Annual / Quarterly Financial Statement • Feb 26, 2025
Annual / Quarterly Financial Statement
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De conformidad con lo dispuesto en el artículo 8.1.b del Real Decreto 1362/2007, de 19 de octubre, los consejeros de Grifols, S.A. (la "Sociedad")
Bajo su responsabilidad que, hasta donde alcanza su conocimiento, las cuentas anuales del ejercicio cerrado a 31 de diciembre de 2024, elaboradas con arreglo a los principios de contabilidad aplicables, ofrecen la imagen fiel del patrimonio, de la situación financiera y de los resultados de la Sociedad y de las empresas comprendidas en la consolidación tomados en su conjunto, y que el informe de gestión incluye un análisis fiel de la evolución y los resultados empresariales y de la posición de la Sociedad y de las empresas comprendidas en la consolidación tomadas en su conjunto, junto con la descripción de los principales riesgos e incertidumbres a que se enfrentan.
En Sant Cugat del Vallés, a 25 de febrero 2025 In Sant Cugat del Vallés, on 25 February 2025
Pursuant to the provisions of article 8.1.b of Royal Decree 1362/2007, of 19 October, the directors of Grifols, S.A. (the "Company")
On their own responsibility that, to the best of their knowledge, the annual accounts for the fiscal year ended on 31 December 2024, prepared in accordance with applicable accounting standards, give a fair view of the net worth, financial situation and results of the Company and of the companies included in its consolidation scope, considered as a whole, and that the director's report contains an accurate analysis of the evolution, business results and position of the Company and of the companies included in its consolidate scope, taken as a whole, together with a description of the main risks and uncertainties which they face.
| Thomas Glanzmann | José Ignacio Abia Buenache | Raimon Grifols Roura |
|---|---|---|
| Chairman | Chief Executive Officer | Board Member |
| Víctor Grifols Deu | Albert Grifols Coma-Cros | Tomás Dagá Gelabert |
| Board Member | Board Member | Board Member |
| Íñigo Sánchez-Asiaín Mardones Board Member |
Anne-Catherine Berner Board Member |
Enriqueta Felip Font Board Member |
| Pascal Ravery | Montserrat Muñoz Abellana | Susana González Rodríguez |
| Board Member | Board Member | Board Member |
| Paul S. Herendeen Board Member |
Núria Martín Barnés Secretary |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| (1) Nature, Principal Activities and Subsidiaries | 1 |
|---|---|
| (2) Basis of Presentation | 1 |
| (3) Business Combinations and Divestments | 11 |
| (4) Significant Accounting Policies | 21 |
| (5) Segment Reporting | 35 |
| (6) Goodwill | 37 |
| (7) Other Intangible Assets | 43 |
| (8) Leases | 44 |
| (9) Property, Plant and Equipment | 45 |
| (10) Equity-Accounted Investees and Joint Business | 46 |
| (11) Financial Assets | 54 |
| (12) Non-current assets held for sale | 56 |
| (13) Inventories | 57 |
| (14) Contract assets | 58 |
| (15) Trade and Other Receivables | 58 |
| (16) Cash and Cash Equivalents | 59 |
| (17) Equity | 59 |
| (18) Earnings Per Share | 65 |
| (19) Non-Controlling Interests | 67 |
| (20) Provisions | 71 |
| (21) Financial Liabilities | 75 |
| (22) Trade and Other Payables | 85 |
| (23) Other Current Liabilities | 86 |
| (24) Net Revenues | 86 |
| (25) Personnel Expenses | 88 |
| (26) Expenses by Nature | 90 |
| (27) Finance Result | 92 |
| (28) Taxation | 92 |
| (29) Other Commitments with Third Parties and Other Contingent Liabilities | 97 |
| (30) Financial Instruments | 102 |
| (31) Balances and Transactions with Related Parties | 115 |
| (32) Environmental Information and Climate Change | 121 |
| (33) Other Information | 123 |
| (34) Subsequent events | 124 |
at 31 December 2024 and 2023 (Expressed in thousands of Euros)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| Assets | Reference | 31/12/2024 | 31/12/2023 (*) | 1/1/2023 (*) |
|---|---|---|---|---|
| Goodwill | Note 6 | 7,403,056 | 6,802,127 | 7,011,909 |
| Other intangible assets | Note 7 | 2,926,132 | 2,832,196 | 2,949,147 |
| Rights of use | Note 8 | 968,304 | 945,240 | 981,260 |
| Property, plant and equipment | Note 9 | 3,341,846 | 3,247,123 | 3,302,858 |
| Investment in equity-accounted investees | Note 10 | 68,996 | 421,763 | 1,497,959 |
| Non-current financial assets measured at fair | ||||
| value | 423,439 | 12,182 | 38,570 | |
| Non-current financial assets at amortized cost | 67,053 | 164,494 | 458,043 | |
| Total non-current financial assets | Note 11 | 490,492 | 176,676 | 496,613 |
| Other non-current contract assets | 59 | — | — | |
| Other non-current assets | Note 10 | 137,141 | 135,633 | 124,191 |
| Deferred tax assets | Note 28 | 341,673 | 300,329 | 174,923 |
| Total non-current assets | 15,677,699 | 14,861,087 | 16,538,860 | |
| Non-current assets held for sale | Note 12 | — | 1,089,856 | 4,969 |
| Inventories | Note 13 | 3,560,098 | 3,482,399 | 3,236,010 |
| Current contract assets | Note 14 | 35,978 | 47,751 | 35,154 |
| Trade and other receivables | ||||
| Trade receivables | 705,452 | 645,113 | 609,081 | |
| Other receivables | 77,556 | 74,933 | 73,181 | |
| Current income tax assets | 52,589 | 47,213 | 56,782 | |
| Trade and other receivables | Note 15 | 835,597 | 767,259 | 739,044 |
| Other current financial assets | ||||
| Current financial assets measured at fair value | 6,064 | 23,644 | 12,629 | |
| Current financial assets at amortized cost | 237,510 | 116,588 | 31,034 | |
| Total current financial assets | Note 11 | 243,574 | 140,232 | 43,663 |
| Other current assets | 72,515 | 73,942 | 82,677 | |
| Cash and cash equivalents | Note 16 | 979,780 | 529,577 | 549,207 |
| Total current assets | 5,727,542 | 6,131,016 | 4,690,724 | |
| Total assets | 21,405,241 | 20,992,103 | 21,229,584 |
(*) Restated figures (Note 2.d)
at 31 December 2024 and 2023 (Expressed in thousands of Euros)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| Equity and liabilities | Reference | 31/12/2024 | 31/12/2023 (*) | 1/1/2023 (*) | |
|---|---|---|---|---|---|
| Share capital | 119,604 | 119,604 | 119,604 | ||
| Share premium | 910,728 | 910,728 | 910,728 | ||
| Reserves | 4,054,505 | 4,040,961 | 4,053,156 | ||
| Treasury stock | (134,448) | (152,748) | (162,220) | ||
| Profit for the year attributable to the Parent | 156,920 | 42,318 | — | ||
| Total shareholder's equity | 5,107,309 | 4,960,863 | 4,921,268 | ||
| Cash Flow hedges | (270) | 998 | (438) | ||
| Other comprehensive Income | (8,787) | (9,117) | (8,084) | ||
| Other comprehensive income from non-current assets held for sale |
— | 1,520 | — | ||
| Other comprehensive income from financial instruments valuation |
Note 11 | (18,351) | — | — | |
| Translation differences | 803,826 | 414,112 | 735,777 | ||
| Other comprehensive expenses | 776,418 | 407,513 | 727,255 | ||
| Equity attributable to the Parent | Note 17 | 5,883,727 | 5,368,376 | 5,648,523 | |
| Non-controlling interests | Note 19 | 2,723,298 | 2,145,319 | 2,327,606 | |
| Total equity | 8,607,025 | 7,513,695 | 7,976,129 | ||
| Liabilities | |||||
| Grants | 13,944 | 13,807 | 15,123 | ||
| Provisions | Note 20 | 125,048 | 116,925 | 110,063 | |
| Non-current financial liabilities | Nota 21 | 9,490,644 | 10,033,604 | 10,074,155 | |
| Other non-current liabilities | 730 | — | 15 | ||
| Deferred tax liabilities | Nota 28 | 1,011,704 | 988,629 | 1,034,823 | |
| Total non-current liabilities | 10,642,070 | 11,152,965 | 11,234,179 | ||
| Provisions | Note 20 | 38,613 | 47,806 | 56,339 | |
| Current other financial liabilities | Note 21 | 676,087 | 1,023,614 | 800,939 | |
| Trade and other payables | |||||
| Suppliers | 852,305 | 822,953 | 787,964 | ||
| Other payables | 210,179 | 133,181 | 114,927 | ||
| Current income tax liabilities | 60,535 | 14,523 | 15,687 | ||
| Total trade and other payables | Note 22 | 1,123,019 | 970,657 | 918,578 | |
| Other current liabilities | Note 23 | 318,427 | 283,366 | 243,420 | |
| Total current liabilities | 2,156,146 | 2,325,443 | 2,019,276 | ||
| Total liabilities | 12,798,216 | 13,478,408 | 13,253,455 | ||
| Total equity and liabilities | 21,405,241 | 20,992,103 | 21,229,584 |
(*) Restated figures (Note 2.d)
for the years ended at 31 December 2024, 2023 and 2022 (Expressed in thousands of Euros)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| Reference | 2024 | 2023 (*) | 2022 (*) | ||
|---|---|---|---|---|---|
| Continuing Operations | |||||
| Net revenue | Note 5 and 24 | 7,212,382 | 6,591,977 | 6,063,967 | |
| Cost of sales | (4,417,844) | (4,108,495) | (3,850,257) | ||
| Gross Margin | 2,794,538 | 2,483,482 | 2,213,710 | ||
| Research and development | (384,036) | (395,282) | (361,140) | ||
| Selling, general and administration expenses Operating Expenses |
(1,255,291) (1,639,327) |
(1,372,665) (1,767,947) |
(1,195,847) (1,556,987) |
||
| Other income | — | 3,042 | 22,235 | ||
| Profit of equity accounted investees with similar activity to that of the Group |
Note 10 | 36,804 | 63,740 | 103,478 | |
| Operating Result | 1,192,015 | 782,317 | 782,436 | ||
| Finance income | 44,423 | 62,430 | 33,859 | ||
| Finance costs | (714,765) | (596,884) | (478,323) | ||
| Dividends | 2,060 | — | — | ||
| Financial cost of sale of trade receivables | Note 15 | (30,782) | (24,993) | (18,201) | |
| Change in fair value of financial instruments | 19,882 | 1,459 | 11,999 | ||
| Impairment of financial assets | (9,081) | — | — | ||
| Exchange differences | (59,756) | (16,386) | 7,725 | ||
| Finance result | Note 27 | (748,019) | (574,374) | (442,941) | |
| Profit/(loss) of other equity accounted investees |
Note 10 | — | (922) | (1,482) | |
| Profit before income tax | 443,996 | 207,021 | 338,013 | ||
| Income tax expense | Note 28 | (231,190) | (43,349) | (90,111) | |
| Consolidated net profit | 212,806 | 163,672 | 247,902 | ||
| Consolidated net profit attributable to: | 212,806 | 163,672 | 247,902 | ||
| Profit attributable to the Parent | 156,920 | 42,318 | 185,035 | ||
| Profit attributable to non-controlling interest | Note 19 | 55,886 | 121,354 | 62,867 | |
| Basic earnings per share (Euros) | Note 18 | 0.23 | 0.06 | 0.27 | |
| Diluted earnings per share (Euros) | Note 18 | 0.23 | 0.06 | 0.27 |
(*) Restated figures (note 2.d)
for the years ended at 31 December 2024, 2023 and 2022 (Expressed in thousands of Euros)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| Reference | 2024 | 2023 (*) | 2022 (*) | |
|---|---|---|---|---|
| Consolidated net profit | 212,806 | 163,672 | 247,902 | |
| Translation differences | 513,450 | (303,352) | 531,238 | |
| Equity accounted investees / Translation differences | Note 10 | (18,466) | (62,191) | (30,771) |
| Other comprehensive income from non-current assets held for sale | (1,520) | 1,520 | — | |
| Cash flow hedges - effective portion of changes in fair value | 2,007 | (20,807) | 40,052 | |
| Cash flow hedges - amounts taken to profit or loss | (3,697) | 22,722 | (44,809) | |
| Tax effect | 423 | (479) | 1,189 | |
| Total other comprehensive (loss) income recognized for the year that may be reclassified subsequently to profit or loss |
492,197 | (362,587) | 496,899 | |
| Gains (losses) from defined benefit plans | 3,231 | (2,842) | (11,776) | |
| Gains (losses) from financial assets measured at fair value through comprehensive income |
(24,468) | — | — | |
| Tax effect | 3,216 | 1,810 | 4,560 | |
| Total other comprehensive income (loss) recognized for the year that will not be reclassified subsequently to profit or loss |
(18,021) | (1,032) | (7,216) | |
| Total Other comprehensive income (loss) for the year | 474,176 | (363,619) | 489,683 | |
| Total comprehensive income (loss) for the year | 686,982 | (199,947) | 737,585 | |
| Total comprehensive income attributable to the Parent | 525,824 | (277,424) | 576,938 | |
| Total comprehensive income attributable to non-controlling interests | 161,158 | 77,477 | 160,647 |
(*) Restated figures (Note 2.d)
31 December 2024, 2023 and 2022 (Expressed in thousands of Euros)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| Reference | 2024 | 2023 (*) | 2022 (*) | |
|---|---|---|---|---|
| Cash flows from operating activities | ||||
| Profit before income tax | 443,996 | 207,021 | 338,013 | |
| Adjustments for: | 1,182,734 | 1,034,458 | 788,272 | |
| Amortization and depreciation | Note 26 | 437,897 | 446,422 | 410,980 |
| Other adjustments: | 744,837 | 588,036 | 377,292 | |
| (Profit) / losses on equity accounted investments | Note 10 | (36,804) | (62,818) | (101,996) |
| Impairment of assets and net provision charges | 73,259 | 100,943 | 69,982 | |
| (Profit) / losses on disposal of fixed assets | 1,378 | 7,182 | (1,731) | |
| Government grants taken to income | (15,254) | (10,260) | (16,440) | |
| Finance cost / (income) | 681,122 | 555,795 | 445,027 | |
| Other adjustments | 41,136 | (2,806) | (17,550) | |
| Change in operating assets and liabilities | 22,376 | (362,843) | (584,351) | |
| Change in inventories | 25,819 | (411,441) | (631,122) | |
| Change in trade and other receivables | (41,883) | (68,815) | (77,494) | |
| Change in current financial assets and other current assets | 9,644 | 12,944 | (2,252) | |
| Change in current trade and other payables | 28,796 | 104,469 | 126,517 | |
| Other cash flows used in operating activities | (746,938) | (659,946) | (543,361) | |
| Interest paid | Note 21(e) | (571,487) | (528,942) | (350,387) |
| Interest received | 10,806 | 13,747 | 4,054 | |
| Income tax paid | (175,563) | (158,854) | (196,436) | |
| Other paid | (10,694) | 14,103 | (592) | |
| Net cash from/(used in) operating activities | 902,168 | 218,690 | (1,427) | |
| Cash flows from investing activities | ||||
| Payments for investments | (701,091) | (433,102) | (2,090,792) | |
| Group companies, associates and business units | Note 3 and 10 | (285,872) | (29,474) | (1,533,264) |
| Property, plant and equipment and intangible assets | (371,367) | (310,320) | (392,872) | |
| Property, plant and equipment | Note 7 | (232,538) | (224,438) | (283,803) |
| Intangible assets | Note 9 | (138,829) | (85,882) | (109,069) |
| Other financial assets | (43,852) | (93,308) | (164,656) | |
| Proceeds from the sale of investments | 1,587,758 | 38,383 | 94,669 | |
| Non-current assets held for sale | Note 11 and 12 | 1,564,256 | — | 91,373 |
| Property, plant and equipment | 23,502 | 23,247 | 3,296 | |
| Other financial assets | — | 15,136 | — | |
| Net cash (used in) investing activities | 886,667 | (394,719) | (1,996,123) | |
| Cash flows from financing activities | ||||
| Proceeds from and payments for equity instruments | — | — | (3,459) | |
| Payments for treasury stock | — | — | (3,459) | |
| Proceeds from and payments for financial liability instruments | (1,352,269) | 170,037 | (168,780) | |
| Issue | 4,006,656 | 1,637,798 | 1,142,760 | |
| Redemption and repayment | (5,247,437) | (1,351,367) | (1,207,253) | |
| Lease payments | Note 8 and 21(e) | (111,488) | (116,394) | (104,287) |
| Dividends | (962) | — | 10,125 | |
| Dividends paid | (962) | — | (592) | |
| Dividends received | Note 10 | — | — | 10,717 |
| Other cash flows used in financing activities | (5,483) | 1,456 | (2,787) | |
| Financing costs included in the amortized cost of the debt | (57,602) | — | — | |
| Other amounts from / (used in) financing activities | 52,119 | 1,456 | (2,787) | |
| Net cash from/(used in) financing activities | (1,358,714) | 171,493 | (164,901) | |
| Effect of exchange rate fluctuations on cash | 20,082 | (15,094) | 35,551 | |
| Net increase / (decrease) in cash and cash equivalents | 450,203 | (19,630) | (2,126,900) | |
| Cash and cash equivalents at beginning of the year | 529,577 | 549,207 | 2,676,107 | |
| Cash and cash equivalents at year end | Note 16 | 979,780 | 529,577 | 549,207 |
(*) Restated figures (Note 2.d)
31 December 2024, 2023 and 2022
(Expressed in thousands of Euros)
| Attributable to shareholders of the Parent | |||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Reference | Accumulated other comprehensive income | ||||||||||||||
| Share Capital |
Share Premium |
Reserves | Profit attributable to Parent |
Interim dividend |
Treasury Stock |
Translation differences |
Other comprehens ive income |
Other comprehens ive income from non current assets held for sale |
Other comprehens ive income from financial instruments valuation |
Cash flow hedges |
Equity to attributable to Parent |
Non controlling interests |
Equity | ||
| Balance at 31 December 2021 | 119,604 | 910,728 | 4,133,388 | 188,726 | — | (164,189) | 333,091 | (869) | — | — | 3,130 | 5,523,609 | 1,793,489 | 7,317,098 | |
| Adjustment due to restatement (Note 2.d) | — | — | (453,700) | (4,399) | — | — | (310) | — | — | — | — | (458,409) | — | (458,409) | |
| Balance at 31 December 2021 (*) | 119,604 | 910,728 | 3,679,688 | 184,327 | — | (164,189) | 332,781 | (869) | — | — | 3,130 | 5,065,200 | 1,793,489 | 6,858,689 | |
| Translation differences | — | — | — | — | — | — | 402,542 | — | — | — | — | 402,542 | 97,780 | 500,322 | |
| Cash flow hedges | Note 30 | — | — | — | — | — | — | — | — | — | — | (3,568) | (3,568) | — | (3,568) |
| Other comprehensive income | — | — | — | — | — | — | — | (7,215) | — | — | — | (7,215) | — | (7,215) | |
| Other comprehensive income / (expense) for the year | — | — | — | — | — | — | 402,542 | (7,215) | — | — | (3,568) | 391,759 | 97,780 | 489,539 | |
| Profit/(loss) for the year | — | — | — | 208,279 | — | — | — | — | — | — | — | 208,279 | 62,867 | 271,146 | |
| Total comprehensive income / (expense) for the year | — | — | — | 208,279 | — | — | — | — | — | — | — | 208,279 | 62,867 | 271,146 | |
| Net change in treasury stock | Note 17(d) | — | — | — | — | — | 1,969 | — | — | — | — | — | 1,969 | — | 1,969 |
| Acquisition / Divestment of non-controlling interests | Note 17(c) and 19 |
— | — | — | — | — | — | — | — | — | — | — | — | 373,468 | 373,468 |
| Other changes | — | — | 4,322 | — | — | — | — | — | — | — | — | 4,322 | 2 | 4,324 | |
| Distribution of 2021 profit: | — | — | — | — | — | — | — | — | — | — | — | — | — | — | |
| Reserves | — | — | 184,327 | (184,327) | — | — | — | — | — | — | — | — | — | — | |
| Dividends | — | — | — | — | — | — | — | — | — | — | — | — | — | — | |
| Interim dividend | — | — | — | — | — | — | — | — | — | — | — | — | — | — | |
| Operations with shareholders or owners | — | — | 188,649 | (184,327) | — | 1,969 | — | — | — | — | — | 6,291 | 373,470 | 379,761 | |
| Balance at 31 December 2022 | 119,604 | 910,728 | 3,868,337 | 208,279 | — | (162,220) | 735,323 | (8,084) | — | — | (438) 5,671,529 | 2,327,606 | 7,999,135 | ||
| Adjustment due to restatement (Note 2.d) | — | — | (216) | (23,244) | — | — | 454 | — | — | — | — | (23,006) | — | (23,006) | |
| Balance at 31 December 2022 (*) | 119,604 | 910,728 | 3,868,121 | 185,035 | — | (162,220) | 735,777 | (8,084) | — | — | (438) 5,648,523 | 2,327,606 | 7,976,129 |
31 December 2024, 2023 and 2022
(Expressed in thousands of Euros)
| Attributable to shareholders of the Parent | |||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Reference | Accumulated other comprehensive income | ||||||||||||||
| Share Capital |
Share Premium |
Reserves | Profit attributable to Parent |
Interim dividend |
Treasury Stock |
Translation differences |
Other comprehens ive income |
Other comprehens ive income from non current assets held for sale |
Other comprehens ive income from financial instruments valuation |
Cash flow hedges |
Equity to attributable to Parent |
Non controlling interests |
Equity | ||
| Balance at 31 December 2022 (*) | 119,604 | 910,728 | 3,868,121 | 185,035 | — | (162,220) | 735,777 | (8,084) | — | — | (438) 5,648,523 | 2,327,606 | 7,976,129 | ||
| Translation differences | — | — | — | — | — | — | (321,565) | — | — | — | — | (321,565) | (43,877) | (365,442) | |
| Cash flow hedges | Note 30 | — | — | — | — | — | — | — | — | — | — | 1,436 | 1,436 | — | 1,436 |
| Other comprehensive income | — | — | — | — | — | — | — | (1,033) | — | — | — | (1,033) | — | (1,033) | |
| Other comprehensive income from non-current assets held for sale | — | — | — | — | — | — | — | — | 1,520 | — | — | 1,520 | — | 1,520 | |
| Other comprehensive income / (expense) for the year | — | — | — | — | — | — | (321,565) | (1,033) | 1,520 | — | 1,436 | (319,642) | (43,877) | (363,519) | |
| Profit/(loss) for the year | — | — | — | 59,315 | — | — | — | — | — | — | — | 59,315 | 121,354 | 180,669 | |
| Total comprehensive income / (expense) for the year | — | — | — | 59,315 | — | — | — | — | — | — | — | 59,315 | 121,354 | 180,669 | |
| Net change in treasury stock | Note 17(d) | — | — | — | — | — | 9,472 | — | — | — | — | — | 9,472 | — | 9,472 |
| Acquisition / Divestment of non-controlling interests | Note 17(c) and 19 |
— | — | (1,525) | — | — | — | — | — | — | — | — | (1,525) | 325 | (1,200) |
| Other changes | — | — | (10,670) | — | — | — | — | — | — | — | — | (10,670) | (260,089) | (270,759) | |
| Distribution of 2022 profit: | — | — | 185,035 | (185,035) | — | — | — | — | — | — | — | — | — | — | |
| Reserves | — | — | — | — | — | — | — | — | — | — | — | — | — | — | |
| Dividends | — | — | — | — | — | — | — | — | — | — | — | — | — | — | |
| Interim dividend | — | — | — | — | — | — | — | — | — | — | — | — | — | — | |
| Operations with shareholders or owners | — | — | 172,840 | (185,035) | — | 9,472 | — | — | — | — | — | (2,723) | (259,764) | (262,487) | |
| Balance at 31 December 2023 | 119,604 | 910,728 | 4,040,961 | 59,315 | — | (152,748) | 414,212 | (9,117) | 1,520 | — | 998 | 5,385,473 | 2,145,319 | 7,530,792 | |
| Adjustment due to restatement (Note 2.d) | — | — | — | (16,997) | — | — | (100) | — | — | — | — | (17,097) | — | (17,097) | |
| Balance at 31 December 2023 (*) | 119,604 | 910,728 | 4,040,961 | 42,318 | — | (152,748) | 414,112 | (9,117) | 1,520 | — | 998 | 5,368,376 | 2,145,319 | 7,513,695 |
31 December 2024, 2023 and 2022
(Expressed in thousands of Euros)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| Attributable to shareholders of the Parent | |||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Accumulated other comprehensive income | |||||||||||||||
| Reference | Share Capital |
Share Premium |
Reserves | Profit attributable to Parent |
Interim dividend |
Treasury Stock |
Translation differences |
Other comprehens ive income |
Other comprehens ive income from non current assets held for sale |
Other comprehens ive income from financial instruments valuation |
Cash flow hedges |
Equity to attributable to Parent |
Non controlling interests |
Equity | |
| Balance at 31 December 2023 (*) | 119,604 | 910,728 | 4,040,961 | 42,318 | — | (152,748) | 414,112 | (9,117) | 1,520 | — | 998 | 5,368,376 | 2,145,319 | 7,513,695 | |
| Translation differences | — | — | — | — | — | — | 389,714 | — | — | — | — | 389,714 | 105,271 | 494,985 | |
| Cash flow hedges | Note 30 | — | — | — | — | — | — | — | — | — | — | (1,268) | (1,268) | — | (1,268) |
| Other comprehensive income | — | — | — | — | — | — | — | 330 | — | — | — | 330 | — | 330 | |
| Other comprehensive income from non-current assets held for sale | — | — | — | — | — | — | — | — | (1,520) | — | — | (1,520) | — | (1,520) | |
| Other comprehensive income from financial instruments valuation | — | — | — | — | — | — | — | — | — | (18,351) | — | (18,351) | — | (18,351) | |
| Other comprehensive income / (expense) for the year | — | — | — | — | — | — | 389,714 | 330 | (1,520) | (18,351) | (1,268) | 368,905 | 105,271 | 474,176 | |
| Profit/(loss) for the year | — | — | — | 156,920 | — | — | — | — | — | — | — | 156,920 | 55,886 | 212,806 | |
| Total comprehensive income / (expense) for the year | — | — | — | 156,920 | — | — | — | — | — | — | — | 156,920 | 55,886 | 212,806 | |
| Net change in treasury stock | Note 17(d) | — | — | — | — | — | 18,300 | — | — | — | — | — | 18,300 | — | 18,300 |
| Acquisition / Divestment of non-controlling interests | Note 17(c) and 19 |
— | — | (9,699) | — | — | — | — | — | — | — | — | (9,699) | (25,519) | (35,218) |
| Other changes | Note 10 | — | — | (19,075) | — | — | — | — | — | — | — | — | (19,075) | 508,212 | 489,137 |
| Distribution of 2023 profit: | — | — | — | — | — | — | — | — | — | — | — | — | — | — | |
| Reserves | — | — | 42,318 | (42,318) | — | — | — | — | — | — | — | — | — | — | |
| Dividends | — | — | — | — | — | — | — | — | — | — | — | — | (65,871) | (65,871) | |
| Interim dividend | — | — | — | — | — | — | — | — | — | — | — | — | — | — | |
| Operations with shareholders or owners | — | — | 13,544 | (42,318) | — | 18,300 | — | — | — | — | — | (10,474) | 416,822 | 406,348 | |
| Balance at 31 December 2024 | 119,604 | 910,728 | 4,054,505 | 156,920 | — | (134,448) | 803,826 | (8,787) | — | (18,351) | (270) 5,883,727 | 2,723,298 | 8,607,025 |
(*) Restated figures (Note 2.d)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Grifols, S.A. (hereinafter the Company) was incorporated with limited liability under Spanish law on 22 June 1987. Its registered and tax offices are in Avinguda de la Generalitat 152-158, 08174 Sant Cugat del Valles, Barcelona. The Company's statutory activity consist of providing corporate and business administration, management and control services, as well as investing in assets and property. Its principal activity involves rendering administrative, management and control services to its subsidiaries.
On 17 May 2006 the Company completed its flotation on the Spanish securities market, which was conducted through the public offering of 71,000,000 ordinary shares of Euros 0.50 par value each and a share premium of Euros 3.90 per share. The total capital increase (including the share premium) amounted to Euros 312.4 million, equivalent to a price of Euros 4.40 per share.
The Company's shares were floated on the Spanish stock exchange IBEX-35 index on 2 January 2008.
All of the Company's shares are listed on the Barcelona, Madrid, Valencia and Bilbao securities markets and on the Spanish Automated Quotation System (SIBE/Continuous Market). On 2 June 2011, Class B non-voting shares (ADRs) were listed on the NASDAQ (USA) and on the Spanish Automated Quotation System (SIBE/Continuous Market).
Grifols, S.A. is the Parent of the subsidiaries listed in Appendix I of this note to the consolidated annual accounts.
Grifols, S.A. and subsidiaries (hereinafter the Group) act on an integrated basis and under common management and their principal activity is the procurement, manufacture, preparation and commercialization of essential plasma medicines, non-plasma therapies and diagnostic solutions.
The main factory locations of the Group's Spanish companies are in Parets del Vallés (Barcelona) and Torres de Cotilla (Murcia), while the US companies are located in Los Angeles (California), Clayton (North Carolina), Emeryville (California), and San Diego (California). Additionally, the Group has manufacturing facilities in Dublin (Ireland), Montreal (Canada) and Dreieich (Germany).
The consolidated annual accounts have been prepared on the basis of the accounting records of Grifols, S.A. and of the Group companies. The consolidated annual accounts for 2024 and its comparative figures have been prepared under International Financial Reporting Standards as adopted by the European Union (IFRS-EU) which for Grifols Group purposes, are identical to the standards as issued by the International Accounting Standard Board (IFRS-IASB) to present fairly the consolidated equity and consolidated financial position of Grifols, S.A. and subsidiaries for 2024, as well as the consolidated results from their operations, consolidated cash flows and consolidated changes in equity for the year then ended.
At their meeting held on 25 February 2025 the Board of Directors of Grifols, S.A. authorized for issue the 2024, consolidated annual accounts.
The figures set out in these consolidated annual accounts are stated in thousand Euro, unless indicated otherwise.
These consolidated annual accounts for 2024 show comparative figures for 2023 and voluntarily show figures for 2022 from the consolidated statement of profit and loss, consolidated statement of comprehensive income, consolidated statement of changes in equity and consolidated statement of cash flows and their corresponding notes thereto. For the purposes of comparing the consolidated statement of profit and loss for 2024, 2023 and 2022 and the consolidated balance sheet for 2024 and 2023, the effects of the application new standards described in note 2 must be taken into account.
The Group adopted IFRS-EU for the first time on 1 January 2004 and has been preparing its annual accounts under International Financial Reporting Standards, as adopted by the European Union (IFRS-EU) as required by Spanish capital market regulations governing the presentation of financial statements by companies whose debt or own equity instruments are listed on a regulated market.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
In accordance with the provision of section 357 of the Irish Companies Act 2014, the Company has irrevocably guaranteed all liabilities of an Irish subsidiary undertaking, Grifols Worldwide Operations Limited (Ireland) (see Appendix I), for the financial year ended 31 December 2024 as referred to in subsection 1(b) of that Act, for the purposes of enabling Grifols Worldwide Operations Limited to claim exemption from the requirement to file their own financial statements in Ireland.
The preparation of the consolidated annual accounts in conformity with IFRS-EU requires management to make judgments, estimates and assumptions that affect the application of Group accounting policies. The following notes include a summary of the relevant accounting estimates and judgments used to apply accounting policies which have the most significant effect on the amounts recognized in the consolidated annual accounts.
No changes have been made to prior year judgments relating to existing uncertainties.
The Group is also exposed to interest rate and currency risks. Refer to sensitivity analysis in note 30.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Appendix I shows details of the percentages of direct or indirect ownership of subsidiaries by the Company at 31 December 2024, 2023 and 2022, as well as the consolidation method used in each case for preparation of the accompanying consolidated annual accounts.
Subsidiaries in which the Company directly or indirectly owns the majority of equity or voting rights have been consolidated. Associates in which the Company owns between 20% or more of the voting rights and over which it has no control but does have significant influence, have been accounted for under the equity method.
Despite the Group has not acquired 100% of Grifols Malaysia Sdn Bhd until November 2024, previously, holding 49% of the shares with voting rights, through a contract with the other shareholder and a pledge on its shares, it controlled the majority of the economic decisions and voting rights of said company, therefore, previously being consolidated too.
On the other hand, the Group holds the 75% of the voting rights of Biotek America LLC ("ITK JV"), a company created as a result of a collaboration with Immunotek GH, LLC (Immunotek) with the aim of building and managing 28 plasma donor centers (see note 10). Such collaboration has been integrated in these consolidated annual accounts as a joint agreement.
The entities Haema Gmbh (formerly Haema AG) and BPC Plasma, Inc., and previously Haema Plasma Kft. until its acquisition in October 2024, of which Grifols does not hold shares, but there exists control over them (see note 19), have been consolidated.
Grifols (Thailand) Ltd. has two classes of shares and the Group, through the class of shares it owns, holds the majority of the voting rights. As a consequence, it has been consolidated.
Mecwins, effective May 2024, ceased to be an associated company of Progenika Biopharma, S.A. as loses its significant influence over its interest.
Changes in associates and jointly controlled entities are detailed in note 10.
In 2024:
During the current financial year 2024, the companies Biotest Italy, S.R.L., Biotest Medical, S.L.U., Biotest Farmaceutica LTDA and Biotest France SAS entered into merger agreements, with the resulting companies being, respectively, Grifols Italia S.p.A., Grifols Movaco, S.A., Grifols Biotest Ltda and Grifols France S.A.R.L.
With effect as of July 25, 2024, Grifols, through its wholly owned subsidiary Grifols Innovation and New Technologies Ltd, reached an agreement to acquire the remaining 20% belonging to the Government of Andorra by an amount of Euros 200 thousands.
With effect as of 31 October 2024, Grifols, through its subsidiary Grifols Worldwide Operations Limited, acquired 100% of the capital of Haema Plasma Kft. from Scranton Plasma, B.V. (an entity related to the Group) for an amount of Euro 35 million, supported by a fairness opinion issued by an independent expert. Given that Grifols already exercised control over that subsidiary prior to the acquisition, the transaction had no impact on Consolidated Statement of Profit and Loss for the 2024 financial year, as it is a transaction with a non-controlling interest in which Grifols retains control over Haema Plasma Kft. (see note 3(e) and note 31). Therefore, the difference between the
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
amount paid and the reduction in the minority interests has been recorded in reserves attributable to the parent company for a negative amount of Euros 14,022 thousand as of December 31, 2024.
With effect as of October 7, 2024, Grifols, through its wholly owned subsidiary Grifols Asia Pacific PTE LTD, reached an agreement to acquire the remaining 51% of shares of Grifols Malaysia SDN BHD by an amount of Euros 16 thousands.
In 2023:
With effect as of 1 January 2023, Grifols Escrow Issuer, S.A., Gripdan Invest, S.L., both wholly-owned subsidiaries, and Grifols, S.A. entered into a merger agreement, with Grifols, S.A. being the surviving company.
This operation has had no impact on the Consolidated Annual Accounts.
With effect as of 1 April 2023, Access Biologicals LLC, Chiquito Acquisition Corp. and Grifols Bio Supplies, Inc., all wholly-owned subsidiaries, entered into a merger agreement, with Grifols Bio Supplies, Inc. being the surviving company.
This operation has had no impact on the Consolidated Annual Accounts.
On 30 June 2023, the company Geotech LLC (D/B/A Medkeeper) has been dissolved.
This operation has had no impact on the Consolidated Annual Accounts.
On 27 July 2023, Grifols reached an agreement to acquire the remaining 10% of shares of Kiro Grifols, S.L. for a total amount of Euros 1,161 thousand. Grifols now owns the 100% of its shares.
On 9 October 2023, Grifols, through its wholly owned subsidiary Grifols Innovation and New Technologies Limited, Inc., reached an agreement to acquire the remaining 51% of shares of AlbaJuna Therapeutics, S.L. for a total amount of 1 Euro (see note 3(c)).
On 1st June 2023, Grifols U.K., Ltd. reached an agreement with Biotest AG to acquire the 100% of shares of Biotest (U.K. Ltd.) for a total amount of Euros 20,079 thousand. With effect 1st November 2023, Biotest (U.K., Ltd.) has transferred its net assets to Grifols U.K., resulting in an amalgamation.
The following companies were formed during 2023 and became part of the Grifols Group consolidated:
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
In 2022:
On 13 January 2022, Grifols, through its wholly owned subsidiary Grifols Innovation and New Technologies Limited, Inc., reached an agreement to acquire 51% of the shares of Albimmune, S.L. for a total amount of Euros 3,000.
On 10 March 2022, Grifols, together with the other shareholders, reached an agreement to sell one hundred percent of the issued and outstanding shares of VCN Bioscience, S.L. for US Dollars 7,700 thousand.
As a result of this divestment, the Group has recognized income of Euros 7,557 thousand in the Consolidated Statement of Profit and Loss.
Effective 1 April 2022, Biomat USA Inc. and Talecris Plasma Resources, Inc. entered into a merger agreement, and the resulting company was Biomat USA, Inc.
On 25 April 2022, and once all regulatory approvals had been obtained, Grifols completed the acquisition of 70.18% of the share capital of Biotest AG and the entire share capital of Tiancheng (Germany) Pharmaceutical Holdings AG, whose current corporate name is Grifols Biotest Holdings GmbH, for Euros 1,460,853 thousand (see note 3).
On 15 June 2022, Grifols, through its wholly owned subsidiary Chiquito Acquisition Corp., exercised a call option to buy the remaining 51% of shares of Access Biologicals LLC for a total of US Dollars 142 million (see note 3 and 10).
Effective 15 December 2022, Grifols México, S.A. de C.V. and Logística Grifols, S.A. de C.V. entered into a merger agreement, and the resulting company was Grifols México, S.A. de C.V.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
As of the date of preparation of these annual financial statements, the following standards published by the IASB and the IFRS Interpretations Committee and adopted by the European Union for application in Europe came into force and, therefore, have been taken into account in the preparation of these consolidated annual accounts:
| Mandatory application for annual periods beginning on or after: |
||||||||
|---|---|---|---|---|---|---|---|---|
| Standards | EU effective date | IASB effective date | ||||||
| IAS 1 | Amendments to IAS 1 Presentation of Financial Statements: - Classification of Liabilities as Current or Non-current Date (issued on 23 January 2020); - Classification of Liabilities as Current or Non-current - Deferral of Effective Date (issued on 15 July 2020); and - Non-current Liabilities with Covenants (issued on 31 October 2022) |
1 January 2024 | 1 January 2024 | |||||
| IFRS 16 | Amendments to IFRS 16 Leases: Lease Liability in a Sale and Leaseback (issued on 22 September 2022) |
1 January 2024 | 1 January 2024 | |||||
| IAS 7 | Amendments to IAS 7 Cash flow statement and NIIF 7 Financial instruments: information to disclose: Financial agreements with suppliers (issued on 25 May 2023). |
1 January 2024 | 1 January 2024 |
The application of these standards and interpretations has had no significant impact on these consolidated annual accounts.
At the date these consolidated annual accounts were authorized for issue, the following IFRS and amendments have been published by the IASB but their application is not mandatory until the future periods indicated below:
| Mandatory application for annual periods beginning on or after: |
||||||
|---|---|---|---|---|---|---|
| Standards | EU effective date | IASB effective date | ||||
| IAS 21 | Amendment to IAS 21 Effects of foreign currency conversions on changes in exchange rates: absence of convertibility |
1 January 2025 | 1 January 2025 | |||
| IFRS 18 | Presentation and Disclosure in Financial Statements (issued on 9 April 2024) |
Pending | 1 January 2027 | |||
| IFRS 19 | Subsidiaries without Public Accountability: Disclosures (issued on 9 May 2024) |
Pending | 1 January 2027 | |||
| IFRS 9 / IFRS 7 |
Amendments to the Classification and Measurement of Financial Instruments (Amendments to IFRS 9 and IFRS 7) (issued on 30 May 2024) |
Pending | 1 January 2026 | |||
| Annual Improvements Volume 11 (issued on 18 July 2024) | Pending | 1 January 2026 | ||||
| IFRS 9 / IFRS 7 |
Contracts Referencing Nature-dependent Electricity – Amendments to IFRS 9 and IFRS 7 (issued on 18 December 2024) |
Pending | 1 January 2026 |
The Group has not applied any of these standards or interpretations in advance of their effective date.
The application of these standards and interpretations would not have significant impact on these consolidated financial statements.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The financial information as of December 31, 2023 presented for comparative purposes, differs from that approved by the Ordinary General Meeting of Shareholders of the Parent Company on June 14, 2024 due to the reclassification between subheadings of the Consolidated Comprehensive Income statement detailed in note 10 and the reasons set out below:
In July 2021, Grifols entered into a collaboration agreement with ImmunoTek GH, LLC (ImmunoTek) to open and manage plasma donation centres. The transaction was implemented through the joint creation of a company in the United States, Biotek America LLC ("ITK JV").
Until 2022, Grifols had recognised its interest in the ITK JV as a financial investment. In 2024, following discussions with the Spanish National Securities Market Commission (CNMV), it was concluded that this agreement should be recognised as a joint operation and therefore the assets, liabilities and results of the jointly controlled entity should be recognised. Consequently, in the consolidated annual accounts at December 31, 2023, the assets and liabilities of the joint operation were integrated in the amount of Euros 151 millions and Euros 191 millions, respectively, recognising a negative adjustment in reserves of Euros 40 millions, net of translation differences. The integration was carried out prospectively from January 1, 2023. This negative adjustment to reserves relates mainly to the losses of Biotek America, LLC in 2021, 2022 and 2023.
To accurately present these losses in the respective income statements for each period, the comparative figures corresponding to the income statement for 2023 and 2022 have been restated in the consolidated financial statements for 2024, the impact of which represents a reduction in results of Euros 23 millions and Euros 17 millions, respectively.
On March 30, 2020, Grifols received shares of Shanghai RAAS Blood Products Co. Limited (hereinafter, "SRAAS") corresponding to 26.2% of its share capital in exchange for having previously delivered shares representing 45% of the economic rights of its subsidiary Grifols Diagnostic Solutions, Inc. (hereinafter "GDS") under the swap agreement entered into with SRAAS in 2019. Grifols therefore held a stake in an associate which in turn holds a stake in the GDS subsidiary.
Since International Financial Reporting Standards (IFRS) do not address the accounting treatment of non-controlling interest when an investment in an associate has a stake in a Group company, Grifols chose the accounting policy to (i) increase the percentage of ownership attributable to Grifols in GDS by the indirect interest Grifols obtained through its stake in SRAAS by 11.79% (26.2% of 45%), thereby reducing the non-controlling interest by that percentage, and (ii) exclude any amount recognized by SRAAS for its stake in GDS from the equity-method investment in SRAAS, as Grifols consolidates 100% of the GDS net assets.
Consequently, due to the accounting policy adopted in March 2020, Grifols had an attributable stake of 66.79% (55% + 11.79%) in GDS, while the non-controlling interest was reduced from 45% to 33.21% amounting to Euros 403 million. This reduction in net equity attributable to the non-controlling interest was offset against consolidated reserves because it was a transaction with minority shareholders without loss of control.
As a result of selling the 20% equity stake in SRAAS in 2024 (see note 12), it has been identified that the initial recognition of the investment in SRAAS should have excluded the amount that SRAAS held in GDS according to Grifols' accounting policy at the transaction date, amounting to Euros 457 million. Therefore, the reduction in equity attributable to non-controlling interest should have decreased the investment in equity-accounted investee in SRAAS instead of affecting consolidated reserves. Consequently, both the stake in SRAAS and consolidated reserves are overvalued by Euros 457 million for the years 2020 to 2023.
The difference between the Euros 457 million and the Euros 403 million initially recorded corresponds to the revaluation of the indirect stake that Grifols acquires in GDS through its stake in SRAAS. This adjustment entails a reduction in consolidated reserves as it is a transaction with a minority shareholder without loss of control.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
In this context, the amounts related to 'Investment in equity-accounted investees', 'Non-current assets held for sale,' and 'Consolidated reserves' as of January 1, 2023 and December 31, 2023, have been restated in the comparative information as detailed in the table below.
Despite this correction resulting in a reduction of consolidated equity by Euros 457 million, it has had no impact on the Consolidated Statements of Profit and Loss; it represents an incorrect accounting treatment without affecting the correct results for each affected financial year. Therefore, the results recognized in the equity-method investment in SRAAS and the results attributable to both the Parent Company and the non-controlling interest in GDS in the consolidated annual accounts from 2020 to 2023 are correctly accounted for. Additionally, following this correction, which decreased the carrying value of the investment in SRAAS, the net gain recorded from the sale of the 20% stake in SRAAS is accurately accounted for in the 2024 financial statements.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The following tables summarize the impacts on the comparative information in the Consolidated Balance Sheet and in the Consolidated Statements of Profit and Loss due to the above:
(Expressed in thousands of Euros)
| Assets | 1/1/2023 | Integration adjustment Biotek America |
Adjustment SRAAS |
Restated 1/1/2023 |
|---|---|---|---|---|
| Rights of use | 897,552 | 83,708 | — | 981,260 |
| Property, plant and equipment | 3,270,937 | 31,921 | — | 3,302,858 |
| Investment in equity-accounted investees | 1,955,177 | — | (457,218) | 1,497,959 |
| Non-current financial assets | 582,175 | (124,132) | — | 458,043 |
| Other non-current assets | — | 124,191 | — | 124,191 |
| Total non-current assets | 16,880,390 | 115,688 | (457,218) | 16,538,860 |
| Inventories | 3,201,357 | 34,653 | — | 3,236,010 |
| Trade and other receivables | 608,688 | 393 | — | 609,081 |
| Other current assets | 81,814 | 863 | — | 82,677 |
| Cash and cash equivalents | 547,979 | 1,228 | — | 549,207 |
| Total current assets | 4,653,587 | 37,137 | — | 4,690,724 |
| Total assets | 21,533,977 | 152,825 | (457,218) | 21,229,584 |
| Equity and liabilities | ||||
| Reserves | 4,534,715 | (24,341) | (457,218) | 4,053,156 |
| Total equity | 5,402,827 | (24,341) | (457,218) | 4,921,268 |
| Translation differences | 735,633 | 144 | — | 735,777 |
| Equity attributable to the Parent | 6,129,938 | (24,197) | (457,218) | 5,648,523 |
| Total equity | 8,457,544 | (24,197) | (457,218) | 7,976,129 |
| Non-current financial liabilities | 9,960,562 | 113,593 | — | 10,074,155 |
| Total non-current liabilities | 11,120,586 | 113,593 | — | 11,234,179 |
| Current financial liabilities | 795,686 | 5,253 | — | 800,939 |
| Trade and other payables | 862,335 | 56,243 | — | 918,578 |
| Other current liabilities | 241,487 | 1,933 | — | 243,420 |
| Total current liabilities | 1,955,847 | 63,429 | — | 2,019,276 |
| Total liabilities | 13,076,433 | 177,022 | — | 13,253,455 |
| Total equity and liabilities | 21,533,977 | 152,825 | (457,218) | 21,229,584 |
(in thousand Euros)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
(Expressed in thousands of Euros)
| Integration adjustment |
Adjustment | Restated | ||
|---|---|---|---|---|
| Assets | 31/12/2023 | Biotek America | SRAAS | 31/12/2023 |
| Investment in equity-accounted investees | 534,970 | — | (113,207) | 421,763 |
| Other non-current assets | 145,522 | (9,889) | — | 135,633 |
| Deferred tax assets | 305,295 | (4,966) | — | 300,329 |
| Total non-current assets | 14,989,149 | (14,855) | (113,207) | 14,861,087 |
| Non-current assets held for sale | 1,433,867 | — | (344,011) | 1,089,856 |
| Inventories | 3,459,277 | 23,122 | — | 3,482,399 |
| Total current assets | 6,451,905 | 23,122 | (344,011) | 6,131,016 |
| Total assets | 21,441,054 | 8,267 | (457,218) | 20,992,103 |
| Equity and liabilities | ||||
| Reserves | 4,482,798 | 15,381 | (457,218) | 4,040,961 |
| Profit for the year attributable to the Parent | 59,315 | (16,997) | — | 42,318 |
| Total equity | 5,419,697 | (1,616) | (457,218) | 4,960,863 |
| Translation differences | 414,068 | 44 | — | 414,112 |
| Equity attributable to the Parent | 5,827,166 | (1,572) | (457,218) | 5,368,376 |
| Total equity | 7,972,485 | (1,572) | (457,218) | 7,513,695 |
| Total trade and other payables | 960,818 | 9,839 | — | 970,657 |
| Total liabilities | 13,468,569 | 9,839 | — | 13,478,408 |
| Total equity and liabilities | 21,441,054 | 8,267 | (457,218) | 20,992,103 |
(in thousand Euros)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
at 31 December 2022
(Expressed in thousands of Euros)
| 2022 | Integration adjustment Biotek America |
Restated 2022 |
|
|---|---|---|---|
| Net revenue | 6,063,967 | — | 6,063,967 |
| Cost of sales | (3,832,437) | (17,820) | (3,850,257) |
| Gross Margin | 2,231,530 | — | 2,213,710 |
| Operating Expenses | (1,551,563) | (5,424) | (1,556,987) |
| Other Income | 22,235 | 22,235 | |
| Profit of equity accounted investees with similar activity to that of the Group | 103,478 | — | 103,478 |
| Operating Result | 805,680 | (23,244) | 782,436 |
| Finance result | (442,941) | (442,941) | |
| Profit/(loss) of equity accounted investees | (1,482) | — | (1,482) |
| Profit before income tax from continuing operations | 361,257 | (23,244) | 338,013 |
| Income tax expense | (90,111) | — | (90,111) |
| Profit after income tax from continuing operations | 271,146 | (23,244) | 247,902 |
| Consolidated profit for the year | 271,146 | (23,244) | 247,902 |
| Profit attributable to the Parent | 208,279 | (23,244) | 185,035 |
| Profit attributable to non-controlling interest | 62,867 | — | 62,867 |
| Basic earnings per share (Euros) | 0.31 | (0.04) | 0.27 |
| Diluted earnings per share (Euros) | 0.31 | (0.04) | 0.27 |
(in thousand Euros)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
at 31 December 2023
(Expressed in thousands of Euros)
| 2023 | Integration adjustment Biotek America |
Restated 2023 |
|
|---|---|---|---|
| Net revenue | 6,591,977 | — | 6,591,977 |
| Cost of sales | (4,097,406) | (11,089) | (4,108,495) |
| Gross Margin | 2,494,571 | — | 2,483,482 |
| Operating Expenses | (1,761,955) | (5,992) | (1,767,947) |
| Other Income | 3,042 | 3,042 | |
| Profit of equity accounted investees with similar activity to that of the Group | 63,740 | — | 63,740 |
| Operating Result | 799,398 | (17,081) | 782,317 |
| Finance result | (574,458) | 84 | (574,374) |
| Profit/(loss) of equity accounted investees | (922) | — | (922) |
| Profit before income tax from continuing operations | 224,018 | (16,997) | 207,021 |
| Income tax expense | (43,349) | — | (43,349) |
| Profit after income tax from continuing operations | 180,669 | (16,997) | 163,672 |
| Consolidated profit for the year | 180,669 | (16,997) | 163,672 |
| Profit attributable to the Parent | 59,315 | (16,997) | 42,318 |
| Profit attributable to non-controlling interest | 121,354 | — | 121,354 |
| Basic earnings per share (Euros) | 0.09 | (0.03) | 0.06 |
| Diluted earnings per share (Euros) | 0.09 | (0.03) | 0.06 |
As a result of the collaboration agreement signed with ImmunoTek GH, LLC, Grifols acquired 7 silos on April 1, 2024 and 7 silos on July 1, 2024, one silo for each plasma center for an amount of US Dollars 134,902 thousand and US Dollars 130,956 thousand, respectively. These transactions enabled Grifols to gain control of the 14 centers as of their acquisition date in 2024, which had previously been considered within a joint operation.
Therefore, Grifols has applied the requirements for a business combination carried out in stages. However, considering that (i) Grifols' effective participation in the joint operation is null and void and (ii) all of the assets and liabilities related to the joint operation are already recognized in the consolidated financial statements, the difference between the consideration paid and the fair value of the assets and liabilities, which does not differ from their carrying amount, has been recognized as provisional goodwill at the date of acquisition.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The aggregate detail of the cost of the business combination and interim goodwill as of the acquisition date is shown below:
| Thousand of Euros | Thousand of US Dollar |
|
|---|---|---|
| Consideration paid | 245,798 | 265,858 |
| Step-up of net assets 1 | — | — |
| Goodwill | 245,798 | 265,858 |
| Adjustments from the acquisition 2 | (12,377) | (13,092) |
| Goodwill, net of adjustments | 233,421 | 252,766 |
11There is no step-up of net of assets since the fair value and the carrying amount do no differ significantly. Additionally, the net assets were previously recognized in the consolidated financial statements as part of the joint operation.
2The adjustments resulting from the acquisition correspond mainly to the elimination of the net balance payable that the silos maintained with Immunotek. The net amount represents the accumulated losses from the silos, which were allocated to Immunotek in accordance with the terms of the contract (see note 10)
The resulting goodwill has been allocated to the Biopharma segment and includes the donor database, licenses and workforce.
The operations of these centers were already consolidated since the beginning of the agreement with Immunotek (see note 10), so there is no impact either on turnover, given that all sales transactions are eliminated in the consolidation process, or on results if both transactions had taken place on January 1, 2024.
On 7 July, 2023, Grifols, through its 100% owned subsidiary Grifols Canada Plasma, Inc. (formerly Prometic Plasma Resources, Inc.), acquired a plasma donation center from Canadian Plasma Resources Corporation which was a business in accordance with IFRS 3. The purchase price was Canadian Dollars 11,558 thousand (Euros 8,018 thousand).
Aggregate details of the cost of the business combination, provisional the fair value of the net assets acquired and the provisional goodwill at the acquisition date are shown below:
| Reference | Thousands of Euros | Thousands of Canadian Dollars |
|
|---|---|---|---|
| Cost of the business combination | |||
| Consideration paid | 8,018 | 11,558 | |
| Total consideration paid | 8,018 | 11,558 | |
| Fair value of net assets acquired | 160 | 231 | |
| Goodwill (excess of the cost of the business combination over the fair value of net assets acquired) |
Note 6 | 7,858 | 11,327 |
(in thousand Euros)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The amounts determined at the acquisition date of the assets acquired are as follows:
| Fair Value | |||
|---|---|---|---|
| Thousands of Euros | Thousands of Canadian Dollars |
||
| Property, plant and equipment | 96 | 138 | |
| Inventories | 64 | 93 | |
| Total Assets | 160 | 231 | |
| Total net assets acquired | 160 | 231 |
The resulting goodwill was allocated to the Biopharma segment and includes the donor database, licenses and workforce. The entire goodwill is considered tax deductible.
On 9 October, 2023, Grifols, through its 100% owned subsidiary Grifols Innovation and New Technologies Limited (GIANT), reached an agreement to acquire the remaining of the 51% of the shares of Albajuna Therapeutics, S.L. (hereinafter "Albajuna") for a total amount of 1 euro.
In 2016, Grifols made a capital investment of Euros 3.75 million in exchange for 30% of the shares of Albajuna Therapeutics, S.L. Since 2018, as a result of a planned investment in accordance with the Shareholders' Agreement of January 2016, Grifols held a 49% of the shares in the company's capital. Albajuna Therapeutics, S.L. is a Spanish research company founded in 2016 whose main activity is the development and manufacture of therapeutic antibodies against HIV.
Aggregate details of the cost of the business combination, the provisional fair value of the net assets acquired and the provisional goodwill at the acquisition date are shown below:
| Reference | Thousands of Euros |
|
|---|---|---|
| Cost of the business combination | ||
| Consideration paid | — | |
| Total consideration paid | — | |
| Fair value of net assets acquired | (1,794) | |
| Goodwill (excess of the cost of the business combination over the fair value of net assets acquired) |
Note 6 | 1,794 |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The amounts determined at the acquisition date of the assets, liabilities and contingent liabilities acquired are as follows:
| Fair Value | |
|---|---|
| Thousands of Euros | |
| Non-current financial assets | 165 |
| Deferred tax assets | 239 |
| Trade and other receivables | 185 |
| Cash and cash equivalents | 86 |
| Total assets | 675 |
| Non-current financial liabilities | (2,300) |
| Current financial liabilities | (164) |
| Trade and other payables | (5) |
| Total Liabilities and contingent liabilities | (2,469) |
| Total net assets acquired | (1,794) |
As future economic benefits cannot be estimated at the acquisition date, the total amount allocated to goodwill has been totally impaired immediately upon recognition (see note 6).
On 31 December 2021, Grifols, through its wholly owned subsidiary Grifols Canada Therapeutics, Inc., acquired all the shares of Prometic Plasma Resources Inc. for a total of Canadian Dollars 11,127 thousand (Euros 7,757 thousand).
Aggregate details of the cost of the business combination, the fair value of the net assets acquired and the goodwill at the acquisition date are shown below:
| Reference | Thousands of Euros | Thousands of Canadian Dollars |
|
|---|---|---|---|
| Cost of the business combination | |||
| Consideration paid | 7,757 | 11,127 | |
| Total consideration paid | 7,757 | 11,127 | |
| Fair value of net assets acquired | 4,933 | 7,075 | |
| Goodwill (excess of the cost of the business combination over the fair value of net assets acquired) |
Note 6 | 2,824 | 4,052 |
At transaction date, total consideration paid was allocated to goodwill, and the amount was restated based on the fair value of the net assets acquired during the following year. Consequently, the amount reflected in note 6 is the movement between both effects, while the amount in the previous table shows the final balance.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The amounts determined at the acquisition date of the assets, liabilities and contingent liabilities acquired are as follows:
| Fair Value | |||
|---|---|---|---|
| Thousands of Euros | Thousands of Canadian Dollars |
||
| Other Intangible Assets | 551 | 791 | |
| Rights of Use | 238 | 341 | |
| Property, plant and equipment | 36 | 51 | |
| Inventories | 71 | 102 | |
| Trade and other reeceivables | 4,603 | 6,602 | |
| Other current assets | 9 | 13 | |
| Cash and cash equivalents | 32 | 46 | |
| Total Assets | 5,540 | 7,946 | |
| Non-current financial liabilities | (32) | (46) | |
| Current financial liabilities | (264) | (379) | |
| Trade and other payables | (311) | (446) | |
| Total Liabilities | (607) | (871) | |
| Total net assets acquired | 4,933 | 7,075 |
The resulting goodwill was allocated to the Biopharma segment and includes the donor database, licenses and workforce.
Grifols Canada Plasma, Inc. acquisition had an impact of Euros 3,933 thousand benefit in the Group result from the acquisition date until the end of fiscal year 2022.
On 1 February 2021, Scranton Plasma B.V. acquired 100% of the shares of Haema Plasma Kft. Scranton Enterprises B.V. (the parent company of Scranton Plasma B.V.) is a shareholder of Grifols.
On 1 February 2021 the Group signed a call option on the shares of Haema Plasma kft, exercisable by the Group only 12 months after signing and with an expiry of 48 months from the date on which the option becomes exercisable. The option price was set at thirteen times EBITDA minus net debt. Grifols did not make any monetary consideration for the purchase option agreement when signing the agreement.
The Group has potential voting rights arising from the option to purchase the shareholding and these are substantive, based on:
The above are indicators of the power that Grifols acquires over this entity, considering that the call option is likely to be exercised and Grifols will have the financial capacity to carry it out.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Consequently, at the time the option became exercisable, the option empowered Grifols, even though it was not yet exercised, and Haema Plasma Kft. was therefore consolidated in Grifols' consolidated financial statements from 2022.
Aggregate details of the cost of the business combination, the fair value of the net assets acquired and the goodwill at the acquisition date are shown below:
| Reference | Thousands of Euros |
Thousands of Hungarian Forint |
|
|---|---|---|---|
| Call option price | 16,948 | 6,228,796 | |
| Total call option price | 16,948 | 6,228,796 | |
| Fair value of net assets acquired | 2,209 | 812,371 | |
| Goodwill (excess of the cost of the business combination over the fair value of net assets acquired) |
Note 6 | 14,739 | 5,416,425 |
Grifols did not give any monetary consideration for this purchase option.
The amounts determined at the date of consolidation of the assets, liabilities and contingent liabilities acquired are as follows:
| Fair Value | ||||
|---|---|---|---|---|
| Thousands of Euros | Thousands of Hungarian Forint |
|||
| Other Intangible assets | 37 | 13,620 | ||
| Rights of Use | 3,421 | 1,257,286 | ||
| Property, plant and equipment | 1,301 | 478,222 | ||
| Other non-current assets | 302 | 110,810 | ||
| Deferred tax assets | 13 | 4,742 | ||
| Inventories | 2,784 | 1,022,926 | ||
| Trade and other receivables | 357 | 131,821 | ||
| Other current assets | 252 | 92,769 | ||
| Cash and cash equivalents | 3,343 | 1,228,356 | ||
| Total Assets | 11,810 | 4,340,552 | ||
| Provisions | (169) | (61,946) | ||
| Non-current financial liabilities | (2,517) | (925,074) | ||
| Current financial liabilities | (4,281) | (1,573,216) | ||
| Trade and other payables | (2,100) | (771,861) | ||
| Other current liabilities | (534) | (196,084) | ||
| Total Liabilities and contingent liabilities | (9,601) | (3,528,181) | ||
| Total net assets acquired | 2,209 | 812,371 |
The resulting goodwill was allocated to the Biopharma segment and includes the donor database, licences and workforce. The entire goodwill is not considered tax deductible.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
On 10 March 2022, Grifols, together with the other shareholders, reached an agreement to sell one hundred percent of the issued and outstanding shares of VCN Bioscience, S.L. for US Dollars 7,700 thousand (Euros 6,901 thousand).
As a result of this divestment, the Group recognized an income of Euros 7,557 thousand under "other income" in the statement of profit and loss. VCN's net assets were derecognised from the consolidated group as of the indicated date.
On 25 April 2022, and once all regulatory approvals were obtained, Grifols completed the acquisition of 70.18% of the share capital of Biotest AG for Euros 1,460,853 thousand. The transaction was structured as follows:
The acquisition was financed through the issuance of bonds in 2021 (see note 21).
The investment in Biotest will significantly strengthen Grifols' capabilities, including its scientific and technical capabilities, helping to strengthen the availability of plasma medicines, its commercial presence and its R&D pipeline. With the opening of 2 new centers, Biotest now has 28 plasma donation centers in Europe.
Aggregate details of the cost of the business combination, the fair value of the net assets acquired and the goodwill at the acquisition date are shown below:
| Reference | Thousands of Euros | |
|---|---|---|
| Cost of the business combination | ||
| Consideration paid | 1,460,853 | |
| Total consideration paid | 1,460,853 | |
| Fair value of net assets acquired | 1,157,229 | |
| Goodwill (excess of the cost of the business combination over the fair value of net assets acquired) |
Note 6 | 303,624 |
The resulting goodwill was allocated to the Biopharma segment.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The amounts determined at the date of consolidation of the assets, liabilities and contingent liabilities acquired are as follows:
| Fair Value | |
|---|---|
| Thousand of Euros | |
| Other Intangible Assets | 1,172,582 |
| Rights of Use | 25,256 |
| Property, plant and equipment | 545,667 |
| Other non-current assets | 13,969 |
| Deferred Tax Assets | 9,109 |
| Inventories | 259,316 |
| Contract Assets | 35,319 |
| Trade and other receivables | 88,249 |
| Other current assets | 25,644 |
| Cash and cash equivalents | 94,662 |
| Total assets | 2,269,773 |
| Non-controlling interests | (356,386) |
| Non-current provisions | (120,298) |
| Non-current financial liabilities | (182,761) |
| Other non-current liabilities | (9) |
| Deferred tax liabilities | (347,192) |
| Current Provisions | (18,239) |
| Current financial liabilities | (35,052) |
| Trade and other payables | (40,489) |
| Other current liabilities | (12,118) |
| Total Liabilities and contingent liabilities | (1,112,544) |
| Total net assets acquired | 1,157,229 |
As part of the purchase price allocation, the company determined that identifiable intangible assets are the research and development projects in progress valued at Euros 946 million, the current product portfolio valued at Euros 202 million as well as certain distribution agreements valued at Euros 24 million.
The fair value of intangible assets was estimated using an income approach and the projected cash flows discounted using rates between 8.6% and 11%. The cash flows were based on estimates used to establish the transaction price and the discount rates applied were compared with reference to the implied rate of return of the transaction model and the weighted average cost of capital.
The fair value of research and development projects in progress involving plasma therapies (Fibrinogen, IgM and IgG) were estimated in accordance with an income approach based on the Multiple-Period Excess Earnings Method for the application of which the results of such projects were adjusted for the probability of success according to the clinical phase of the project at the date of the transaction.
The current product portfolio comprised regulatory approvals, trademarks, patient relationships and physician relationships related to products currently marketed by Biotest in the moment of the transaction. The distribution agreements identified as intangible assets relate to the distribution of certain products in different geographic regions. In both cases, the fair value was determined using the Multiple-Period Excess Earnings Method.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Research and development projects in progress, the current product portfolio and distribution agreements are amortized on a straight-line basis over an average period of 20, 30 and 7.5 years, respectively.
If the acquisition had taken place as of January 1, 2022, the revenue would have changed by Euros 154,846 thousand and the group result by Euros (15,434) thousand.
Biotest Group's acquisition had an impact of Euros 15,605 thousand loss in the Group result from the acquisition date until the end of fiscal year 2022.
The Group recognized under the heading "Selling, general and administration expenses" in the consolidated statement of profit and loss an amount of Euros 23,600 thousand of transaction costs.
On 15 June 2022, Grifols, through its wholly owned subsidiary Chiquito Acquisition Corp., acquired the remaining 51% of the shares of Access Biologicals LLC, by exercising the call option for a total of US Dollars 142 million. With the acquisition of 100% of the stake, Grifols obtained control over Access Biologicals LLC and was therefore considered a group company and consolidated under the full consolidation method. The difference between the fair value of the previous shareholding and the recognised carrying amount was Euros 72,984 thousand (US Dollars 77,209 thousand), and a gain of this amount was recognised under " Profit/(loss) of equity accounted investees " in the consolidated statement of profit and loss (see note 10).
Access Biologicals LLC core business is the collection and manufacture of an extensive portfolio of biological products. Combined with a closed materials sourcing process, it provides support services for different markets such as in-vitro diagnostics, biopharmaceuticals, cell culture and diagnostic research and development.
Aggregate details of the cost of the business combination, the fair value of the net assets acquired and the goodwill at the acquisition date are shown below:
| Reference | Thousands of Euros |
Thousands of US Dollars |
|
|---|---|---|---|
| Cost of the business combination | |||
| Purchase of the first 49% | 48,218 | 51,010 | |
| Purchase of the remaining 51% (present value) | 134,742 | 142,544 | |
| Total consideration paid | 182,960 | 193,554 | |
| Gain on the previously held investment | 72,984 | 77,209 | |
| Accumulated gain for equity method before acquisition date | 8,256 | 8,735 | |
| Step-up of the previously held investment | 81,240 | 85,944 | |
| Fair value of net assets acquired | (83,366) | (88,193) | |
| Goodwill (excess of the cost of the business combination over the fair value of net assets acquired) |
Note 6 | 180,834 | 191,305 |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The amounts determined at the date of consolidation of the assets, liabilities and contingent liabilities acquired are as follows:
| Fair Value | ||||
|---|---|---|---|---|
| Thousands of Euros | Thousands of US Dollars |
|||
| Other Intangible Assets | 82,080 | 86,832 | ||
| Property, plant and equipment | 2,589 | 2,739 | ||
| Other non-current assets | 75 | 79 | ||
| Inventories | 16,836 | 17,811 | ||
| Trade and other receivables | 7,522 | 7,958 | ||
| Other current assets | 1,529 | 1,618 | ||
| Cash and cash equivalents | 2,987 | 3,160 | ||
| Total Assets | 113,618 | 120,197 | ||
| Trade and other payables | (7,249) | (7,669) | ||
| Deferred tax liabilities | (22,981) | (24,312) | ||
| Other non-current liabilities | (22) | (23) | ||
| Total Liabilities and contingent liabilities | (30,252) | (32,004) | ||
| Total net assets acquired | 83,366 | 88,193 |
The resulting goodwill was allocated to the Bio-Supplies segment.
As part of the purchase price allocation, the Company determined that identifiable intangible assets are customer relationships.
Customer relationships were valued using the Multiple-Period Excess Earnings Method, for the application of which a discount rate of 8.1% was considered and a decline rate resulting in an average useful life of 14 years. The cash flows were based on estimates used to establish the transaction price and the discount rate applied was compared with reference to the implied rate of return of the transaction model and the weighted average cost of capital. The excess of the purchase price over the estimated fair value of the net assets acquired was recorded as goodwill. The factors contributing to its recognition were the acquired workforce as well as the expected benefits from the combination of the Group's activities.
If the acquisition had taken place as of January 1, 2022, the consolidated revenue would have changed by Euros 4,402 thousand and the Group result by Euros 1,819 thousand.
Access Biologicals LLC acquisition had an impact of Euros 9,479 thousand benefit in the Group result from the acquisition date until the end of fiscal year 2022.
The Group recognized under operating expense in the consolidated statement of profit and loss an amount of Euros 486 thousand of transaction costs.
In July 2022, Grifols closed an agreement to sell in cash substantially all of the assets of its subsidiary Goetech LLC, whose trade name is MedKeeper, for a US Dollars 91,635 thousand Enterprise Value (Euros 90,002 thousand). MedKeeper develops and markets innovative mobile and cloud-based IT applications aimed at helping hospital pharmacies boost productivity, process safety and compliance.
As a consequence of this divestment, the Group recognized an income of Euros 23,106 thousand in the Statements of Profit and Loss account. Goetech's net assets were derecognized from the consolidated group as of the indicated date.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Subsidiaries are considered to be those over which the Group exercises control. A subsidiary is controlled when, due to its involvement in it, it is exposed, or has the right, to variable returns and has the capacity to influence such returns through the power it exercises over it.
The income, expenses and cash flows of subsidiaries are included in the consolidated annual accounts from the date of acquisition, which is the date on which the Group effectively obtains control of the subsidiaries. Subsidiaries are excluded from consolidation from the date on which control is lost.
Transactions and balances with Group companies and unrealized gains or losses have been eliminated in consolidation.
The accounting policies of the subsidiaries have been adapted to the Group's accounting policies for transactions and other events that, being similar, have occurred in similar circumstances.
The financial statements of the subsidiaries used in the consolidation process are as of the same reporting date and the same period as those of the Parent Company.
Appendix I includes information on the subsidiaries included in the Group's consolidation.
The acquisition method is used to account for the acquisition of businesses in a business combination. The acquisition date is the date on which the Group obtains control of the acquired business.
The acquisition cost of a business is determined at the acquisition date and comprises (i) the fair values of assets acquired, (ii) liabilities incurred or assumed, (iii) equity instruments issued, (iv) the fair value of any asset or liability resulting from a contingent consideration arrangement and (v) the fair value of any previous interest in the business. Any disbursement that is not part of the exchange for the acquired business is excluded.
Acquisition-related costs are expensed as incurred.
The Group recognizes identifiable assets acquired and liabilities and contingent liabilities assumed at fair value at the acquisition date. Non-current assets held for sale, liabilities for employee compensation, transactions with payments based on equity instruments, deferred tax assets and liabilities and right-of-use assets and liabilities and lease liabilities are excluded from the application of this criterion.
The excess of the consideration transferred the amount of any non-controlling interest in the acquired business and the acquisition-date fair value of any previous interest in the acquired business over the fair value of the identifiable net assets is recorded as goodwill. If these amounts are less than the fair value of the identifiable net assets of the acquired subsidiary, the difference is recognized in profit or loss as a bargain purchase.
When settlement of any part of the cash consideration is deferred, amounts payable in the future are discounted to their present value at the date of exchange.
Contingent consideration is classified as equity or a financial liability. Amounts classified as a financial liability are subsequently remeasured at fair value with changes in fair value recognized in profit or loss.
When the business combination could only be determined on a provisional basis, the identifiable net assets are initially recorded at their provisional values, recognizing the adjustments made during the measurement period as if they had been known at the acquisition date, restating comparative figures for the previous year, if applicable. The adjustments to the provisional values only incorporate information relating to facts and circumstances that existed at
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
the acquisition date and which, had they been known, would have affected the amounts recognized at that date. The measurement period should not exceed twelve months from the date of acquisition.
If the business combination is carried out in stages, the acquisition-date carrying amount of the previously held equity interest of the acquiree is remeasured at its acquisition-date fair value, with any resulting gain or loss recognized in profit or loss.
Non-controlling interests in subsidiaries are recorded at the acquisition date at their percentage of interest in the fair value of the identifiable net assets, without considering potential voting rights. In addition, the profit or loss for the year and each component of other comprehensive income allocated to the non-controlling interest is allocated in proportion to its percentage of ownership. Non-controlling interests in the results and equity of subsidiaries are shown separately in the consolidated statement of profit and loss, the consolidated statement of comprehensive income, the consolidated statement of changes in equity and the consolidated balance sheet, respectively.
The increase and reduction of non-controlling interests in a subsidiary while maintaining control is recognized as an equity transaction in reserves.
Associated entities are those over which the Group exercises significant influence, understood as the capacity to intervene in financial and operating decisions, without the existence of control or joint control.
Investments in associates are initially recognized at acquisition cost, including costs directly attributable to the acquisition and any active or passive contingent consideration that depends on future events or the fulfillment of certain conditions.
Subsequently, investments in associates are accounted for by the equity method from the date on which significant influence exists until the date on which the Company can no longer justify the existence of significant influence.
The excess between the cost of the investment and the Group's share of the fair values of the identifiable net assets is recorded as goodwill, which is included in the carrying amount of the investment. The shortfall, once the amounts of the cost of the investment and the identification and valuation of the net assets of the associate have been evaluated, is recorded as income in the determination of the investor's share in the results of the associate for the year in which it was acquired.
The accounting policies of the associated companies have been subject to time and valuation standardization in the same terms as those referred to in the subsidiaries.
The Group's share in the profits or losses of associates obtained from the date that the significant influence exists is recorded as an increase or decrease in the value of the investments with a credit or debit to "Profit of equity accounted investees with similar activity to that of the Group" when the investee companies carry out the same activity as the corporate purpose of the Group described in note 1 and, otherwise, in "Profit /(loss) of equity accounted investees". Likewise, the Group's share in the other comprehensive income of associates obtained since date that the significant influence exists is recorded as an increase or decrease in the value of the investments in associates, with the balancing entry by nature being recognized in other comprehensive income. Dividend distributions are recorded as decreases in the value of investments.
When the Group's share of losses on an equity accounted investment equals or exceeds its interest in the entity, the Group does not recognize additional losses unless it has incurred obligations or made payments on behalf of the other entity.
The Group's share in the profits or losses of associates and changes in equity is determined on the basis of the ownership interest at year-end, without considering the possible exercise or conversion of potential voting rights. However, the Group's share is determined considering the possible exercise of potential voting rights and other derivative financial instruments that, in substance, grant current access to the economic benefits associated with ownership interests, i.e. the right to participate in future dividends and changes in the value of associates.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
After applying the equity method, the Group assesses whether there is objective evidence of impairment of the net investment in the associate. Some of the main evidence include significant cumulative losses, contractual default, financial difficulties and adverse changes in technology, industry or economy affecting the associate. The impairment calculation is determined by comparing the carrying amount of the net investment in the associate with its recoverable amount, where recoverable amount is the higher of value in use or fair value less costs of disposal. In this regard, the value in use is calculated based on the Group's share of the present value of the estimated cash flows from ordinary activities and the amounts that could result from the final disposal of the associate. The recoverable amount of the investment in an associate is assessed in relation to each associate (see note 10),unless it does not constitute a cashgenerating unit (CGU). Impairment losses are not allocated to goodwill or other assets implicit in the investment in associates arising from the application of the acquisition method. In subsequent years, reversals of the value of investments are recognized against income, to the extent that there is an increase in the recoverable value. Impairment losses are presented separately from the Group's share in the results of associates.
Appendix I includes information on subsidiaries and associates included in the Group's consolidation.
Joint arrangements are those in which there is a contractual agreement to share control over an economic activity, so that decisions on the relevant activities require the unanimous consent of the Group and the other participants. Investments in joint arrangements are classified as joint operations or joint ventures, depending on the contractual rights and obligations of each investor, rather than the legal structure of the joint arrangement.
Joint transactions are considered when the participants in the joint arrangement are entitled to the assets and obligations in respect of the liabilities. This type of arrangement is consolidated proportionally integrating the assets and liabilities related to the transaction as described in note 10.
Joint ventures are those when the participants in the agreement have a right to the net assets. This type of arrangement is included in the consolidated financial statements using the equity method, as described in note 10.
Transactions in foreign currencies are translated to the functional currency using the average exchange rate of the previous month provided that it does not differ significantly from the exchange rate at the date of the transaction. Foreign currency gains and losses resulting from the settlement of these transactions and from the translation of monetary assets and liabilities denominated in foreign currencies at closing exchange rates are recognized in profit or loss except when there are qualified cash flow hedges and qualified net investment hedges that are deferred to equity.
The effect of exchange rate changes on cash and cash equivalents denominated in foreign currencies is presented separately in the statement of cash flows as "Effect of exchange rate changes on cash".
The translation of foreign operations whose functional currency is not that of a hyperinflationary country has been made by applying the following criteria:
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
After initial recognition, goodwill is recorded at cost, less any accumulated impairment loss, which is not reversible. Goodwill is not amortized, but is tested for impairment on an annual basis or more frequently in the event that events indicative of a potential loss in the value of the asset have been identified. For these purposes, goodwill resulting from business combinations is allocated to each of the cash generating units (CGUs) or groups of CGUs that are expected to benefit from the synergies of the combination and the criteria referred to in note 6 are applied. CGUs or groups of CGUs are identified at the lowest level that goodwill is controlled for the purpose of internal management (note 6).
Intangible assets are recorded at cost (acquisition or development) or at fair value when acquired in a business combination, less accumulated amortization and any accumulated impairment losses.
Any costs incurred during the research phase of projects are recognized as an expense when incurred.
Costs related to development activities for internally generated intangible assets are capitalized to the extent that:
In relation to the development costs of new products or drugs, they are capitalized as long as their economic profitability is reasonably assured and when they are either in a pivotal phase or correspond to projects related to products that are currently being marketed in various markets, in both cases with expected technical feasibility. Development costs previously recognized as an expense are not recognized as an asset in a subsequent period.
The separate acquisition or through a business combination of an research and development project in progress is capitalized in any case, in accordance with the provisions of IAS 38, since the price paid for the acquisition reflects expectations about the probability that the future economic benefits of the asset are used by the Group. Subsequent costs are recorded following the provisions for internally generated intangible assets.
The Group amortizes its intangible assets with finite useful lives by distributing the cost of the assets on a straightline basis according to the following criteria:
| Amortisation method Rates |
||
|---|---|---|
| Development expenses | Straight line | 10% |
| Concessions, patents, licenses, trademarks and similar | Straight line | 4% - 20% |
| Computer software | Straight line | 33% |
| Currently marketed products | Straight line | 3% - 10% |
Intangible assets with indefinite useful lives are not subject to amortization but are tested for impairment at least once a year.
The Group reviews the useful lives of intangible assets at the end of each year. Changes in the initially established criteria are recognized as a change in estimate.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Property, plant and equipment are stated at cost, less accumulated depreciation and, if applicable, accumulated impairment losses.
Cost includes, among other items, direct labor costs used in the construction of the asset and a portion of the costs indirectly attributable to the asset.
Finance costs incurred that are directly attributable to the acquisition or construction of the asset until the asset is ready for use also form part of the cost.
Likewise, expansion or improvement costs are included as an increase in the value of the asset when they represent an increase in its capacity or an extension of its useful life. However, maintenance costs are recognized in income when incurred.
Depreciation of property, plant and equipment is provided on a straight-line basis over the estimated useful lives of the assets, less their residual value.
Depreciation of property, plant and equipment is determined by applying the following criteria:
| Depreciation method | Rates | |
|---|---|---|
| Buildings | Straight line | 1% - 3% |
| Other property, technical equipment and machinery | Straight line | 4%-10% |
| Other property, plant and equipment | Straight line | 7% - 33% |
The Group reviews the residual value, useful life and depreciation method of property, plant and equipment at the end of each reporting period. Changes in the initially established criteria are recognized as a change in estimate.
The determination of whether a contract is or contains a lease is based on an analysis of the contractual arrangement and requires an assessment of whether the lessee has the right to control the use of the identified asset and to obtain all of the economic benefits from the use of the asset throughout the lease term.
The lease term is the non-cancelable period considering the initial term of each contract unless the Group has a unilateral extension or termination option and there is reasonable certainty that such option will be exercised in which case the corresponding extension or early termination term will be considered.
In lease contracts where the Group acts as lessee, it is recognized at the lease commencement date (i.e. the date on which the underlying asset is available for use):
Lease liabilities include fixed lease payments less any incentives, as well as variable payments that depend on an index or interest rate known at the date of inception of the lease. Also included is the exercise price of the purchase option when the lessee is reasonably certain of exercising it. After initial recognition, the liability is increased by the interest on the lease liability and reduced by the payments made. The liability is also remeasured if there are changes in the amounts payable and the lease terms. Payments included in the lease payments corresponding to maintenance, electricity, water, gas, security, cleaning, among others, are not part of the lease liability and are recognized as an expense.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The incremental borrowing rate is determined taking into account: (i) geographic areas, (ii) financial term, (iii) lease term, (iv) risk-free rate as reference rate and (v) financial spread.
Rights-of-use assets are measured at cost, less accumulated amortization and impairment losses (if any) and adjusted as a result of the remeasurement of the lease liability. Cost includes the amount of the initial valuation of the lease liability, as well as any amounts previously paid to the lessor prior to or at the commencement date of the lease less any incentives received by the lessor and estimated costs to decommission the leased asset. Amortization of rights of use is provided on a straight-line basis over the shorter of the estimated useful life of the asset or the lease term.
The Group applies the exception to recognition for those contracts where the lease term is 12 months or less or where the value of the leased asset (individually) when new, is less than US 5,000 Dollars or its equivalent in another currency. Consequently, in these cases, the amounts accrued will be recognized as an expense during the lease term.
When the Group acts as lessor, it classifies contracts between operating and finance leases. Leases in which the Group acts as lessor while retaining a significant portion of the risks and rewards incidental to ownership of the leased asset are treated as operating leases. Otherwise, the lease is treated as a finance lease.
Goodwill and intangible assets that have an indefinite useful life are not subject to amortization and are tested for impairment annually, or more frequently in the event of events or changes in circumstances that indicate that they may be impaired.
Other assets are tested for impairment whenever events or changes in circumstances indicate that the carrying amount may not be recoverable.
When the recoverable amount is less than the carrying amount of the asset, an impairment loss is recognized in the consolidated statement of profit and loss for the difference between both amounts.
The recoverable amount is the higher of an asset's fair value less costs of disposal and the estimated value in use based on discounted future cash flows expected to arise from the use of the asset. The estimate of value in use considers expectations about possible variations in the amount or timing of cash flows, the time value of money, the price to be paid for bearing the uncertainty related to the asset and other factors that affect the valuation of future cash flows related to the asset.
For the purpose of assessing impairment losses, assets are grouped at the lowest levels for which there are separately identifiable cash inflows that are largely independent of the cash inflows of other assets or groups of assets (cash generating units). Impairment losses on non-financial assets (other than goodwill) are reviewed for possible reversal at the end of each reporting period.
Losses related to the impairment of CGUs are initially allocated to reduce, if applicable, the value of goodwill attributed to the CGU and then to the other assets of the CGU, pro rata based on the carrying amount of each asset, with the limit for each asset being the higher of its fair value less costs of disposal, its value in use and zero.
Impairment losses related to goodwill are not reversible.
The classification of financial assets is determined based on the characteristics of the contractual cash flows of those assets and the business model that represents how the financial assets are managed to achieve a particular business objective. In determining whether the cash flows are obtained through the receipt of contractual cash flows from the
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
assets, consideration is given to the frequency, value and timing of sales in prior periods, the reasons for those sales and expectations regarding future sales activity. This information provides indicative data on how the Group's stated objective regarding the management of financial assets is achieved and, more specifically, how cash flows are obtained.
Therefore, financial assets are classified according to the following valuation categories based on the business model and are only reclassified when, and only when their business model for managing them changes:
a) Financial assets at amortized cost: includes financial assets, including those admitted to trading on an organized market, for which the Group holds the investment under a business model whose objective is to hold financial assets to receive cash flows from the execution of the contract, and the contractual terms of the asset give rise, at specified dates, to cash flows that are solely collections of principal and interest on the principal amount outstanding.
In general, the following are included in this category:
i) Trade receivables: arising from the sale of goods or the rendering of services for trade transactions with deferred payment, and
ii) Receivables from non-trade operations: these arise from loans or credits granted by the Group whose collections are of a determined or determinable amount.
Financial assets are recorded, in general terms, initially at the fair value of the consideration given plus directly attributable transaction costs. However, transaction costs directly attributable to assets recorded at fair value through profit or loss are recognized in the statement of profit and loss for the year.
Financial assets at amortized cost are recorded by applying this valuation criterion, charging to the statement of profit and loss the interest accrued by applying the effective interest rate method.
Financial assets included in the fair value category through other comprehensive income are recorded at fair value, without deducting any transaction costs that may be incurred in their disposal. Changes in fair value are recorded directly in equity until the financial asset is derecognized or impaired, at which time the amount so recognized is taken to the statement of profit and loss.
Financial assets at fair value through profit or loss are measured at fair value and the result of changes in fair value is recorded in the statement of profit and loss.
Financial assets are derecognized when the rights to receive cash flows related to them have expired or have been transferred and the Group has substantially transferred the risks and rewards of ownership. Similarly, they are
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
disposed from the balance sheet when there are transfers of collection rights, whose certain risks are shared with the factor, such as the risk of default, but exists a transfer of control to the factor, understood as the unilateral capacity to sell those assets to a non-related third party without the necessity of enforcing additional restrictions to the sale.
The Group assesses, on a prospective basis, the expected credit losses associated with its debt instruments carried at amortized cost and at fair value through other comprehensive income The methodology applied for impairment depends on whether there has been a significant increase in credit risk.
For trade receivables, the Group applies the simplified approach permitted by IFRS 9 which requires expected losses to be recorded from the initial recognition of the receivables, so that the Group determines expected credit losses as a probability-weighted estimate of such losses over the expected life of the financial instrument.
The practical solution used is the use of a provisioning matrix based on segmentation into homogeneous asset groups, applying historical information on default rates for these groups and applying reasonable information on future economic conditions.
Default rates are calculated based on current default experience over the past year, as it is a very dynamic market, and are adjusted for differences between current and historical economic conditions and considering projected information, which is reasonably available.
Financial liabilities assumed or incurred by the Group are classified in the following measurement categories:
a) Financial liabilities at amortized cost: are those debits and payables of the Group that have arisen from the purchase of goods and services for trading operations, or those which, without having a commercial origin, not being derivative instruments, arise from loan or credit operations received by the Group.
These liabilities are initially measured at the fair value of the consideration received, adjusted for directly attributable transaction costs. Any difference between the amount received and its repayment value is recognized in the consolidated statement of profit and loss during the repayment period of the debt, applying the effective interest rate method.
b) Financial liabilities at fair value through profit or loss.
Liability derivative financial instruments are measured at fair value, following the same criteria as those corresponding to financial assets at fair value through profit or loss described in the preceding section.
The Group derecognizes financial liabilities when the obligations that generated them are extinguished, particularly in commercial transactions when payment is made to the supplier for goods and services.
Assets and liabilities are presented separately in the balance sheet and are only presented at their net amount when the Group has the enforceable right to offset the recognized amounts and, in addition, intends to settle the amounts on a net basis or to realize the asset and settle the liability simultaneously.
The Group holds financial assets, mainly equity instruments, which are measured at fair value. When Group management has opted to present gains and losses in the fair value of equity investments in other comprehensive income, after initial recognition, the equity instruments are measured at fair value, recognizing the gain or loss in other comprehensive income. Amounts recognized in other comprehensive income are not reclassified to profit or loss, but are reclassified to reserves when the instruments are derecognized. Dividends from such investments continue to be recognized in profit or loss as other income when the Group's right to receive payments is established.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Financial derivatives are recognized at fair value at the date of the contract and at each year-end. The method for recognizing the gain or loss depends on whether the derivative is classified as a hedging instrument, and if so, the nature of the hedged asset.
For accounting purposes, they are classified as follows:
Hedge effectiveness is determined at the inception of the hedging relationship, and through periodic prospective effectiveness assessments to ensure that there is an economic relationship between the hedged item and the hedging instrument.
In derivatives such as the euro/Dollar cross-currency swap, the Group uses the hypothetical derivative method to assess effectiveness. This hypothetical derivative is constructed without the inclusion of credit risk and currency spread. Under the hypothetical derivative method, the cumulative change in the fair value of the actual currency swap, excluding the effect of the currency spread, will be compared to the cumulative change in the fair value of the hypothetical swap. Therefore, the hypothetical derivative is constructed as a cross-currency swap with fixed euro payment, fixed U.S. Dollar receipt without the inclusion of credit risk and foreign currency spread and with a fair value of zero at the date of designation.
At the inception of the hedging relationship, the Group documents the economic relationship between the hedging instruments and the hedged items, including whether changes in cash flows of the hedging instruments are expected to offset changes in cash flows of the hedged items. The Group documents its risk management objective and strategy for undertaking its hedging transactions.
The effective portion of changes in the fair value of derivatives designated and classified as cash flow hedges is recognized in equity under "Cash flow hedge reserve". In the case of cross-currency swaps, the currency spread of the hedging relationship is excluded and treated as hedging costs in equity. The gain or loss corresponding to the ineffective portion is recognized immediately in profit or loss for the year under the heading "Change in fair value of financial instruments".
Amounts accumulated in the hedging reserve included in shareholders' equity are transferred to profit or loss when the hedged item affects profit or loss or when ineffectiveness is identified.
The fair value of derivatives designated as hedges is detailed in note 30 Movements in the hedging reserve included in shareholders' equity are shown in note 17(c).
When derivatives do not meet the criteria for hedge accounting, they are classified as "held for trading". Changes in fair value are recognized immediately in the consolidated statement of profit and loss.
In addition, Grifols assesses whether embedded derivatives are present in contracts and financial instruments. Financial instruments that combine a host contract and a financial derivative (embedded derivative) are known as hybrid financial instruments. In hybrid financial instruments, the Group assesses whether the risks and characteristics of the derivative are closely related to those of the host contract. If it is determined that the value of the derivative is closely related to the fair value of the contract, the Group does not account for the derivative separately. Conversely, if the risks and characteristics of the derivative are not closely related to those of the host contract and the host contract is not measured at fair value, the derivative is recognized and accounted for separately recognizing the changes in fair value in the Consolidated Statements of Profit and Loss. Currently there are no separate financial instruments from the host contract.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The acquisition of treasury stock is recorded at acquisition cost, reducing equity until the time of disposal. Gains or losses on the disposal of treasury stock are recorded under "Reserves" in the consolidated balance sheet. Transaction costs related to own equity instruments, net of taxes, are recorded as a reduction of equity.
Inventories are stated at the lower of weighted average cost or net realizable value. Net realizable value is the estimated selling price in the normal course of business, less the estimated costs to complete production and those necessary to make the sale. For raw materials and other supplies it is the replacement cost.
The cost includes direct materials, direct labor and an appropriate proportion of indirect variable and fixed costs, the latter being allocated on the basis of the normal working capacity of the means of production. The cost of plasma inventory includes the amount delivered to donors, or the amount invoiced by the seller when purchased from third parties, as well as the cost of products and devices used in the collection process, and rental and storage costs. The costs of purchased inventories are determined after deducting discounts and rebates when it is probable that the conditions determining their concession will be met. Indirect costs such as management and administrative overheads are recognized as expenses in the period in which they are incurred.
Any previously recognized inventory impairment adjustment is reversed against income under "Cost of sales" when the circumstances that caused the impairment no longer exist or when there is clear evidence of an increase in the net realizable value as a result of a change in economic circumstances. The reversal of the inventory impairment adjustment is limited to the lower of cost and the new net realizable value of inventories.
Cash and cash equivalents include cash on hand, demand deposits with banks, other short-term highly liquid investments with an original maturity of three months or less that are readily convertible to known amounts of cash and which are subject to an insignificant risk of changes in value.
Government grants are recognized when there is reasonable assurance that the conditions attached to the grant will be met and that the grant will be collected.
Non-refundable capital grants are recorded on the liability side of the consolidated balance sheet at the original amount granted and are recognized in the consolidated statement of profit and loss as the related assets financed are depreciated.
Grants received as compensation for expenses or losses already incurred or for the purpose of providing immediate financial support not related to future expenses are credited to the consolidated statement of profit and loss.
Financial liabilities that incorporate implicit aid in the form of the application of below-market interest rates are recognized initially at fair value. The difference between this value, adjusted where appropriate for the costs of issuing the financial liability and the amount received, is recorded as a government grant based on the nature of the grant.
The Group records the contributions to be made to defined contribution plans as they accrue. The amount of accrued contributions is recorded under "Personnel expenses" in the consolidated statement of profit and loss in the year to which the contribution relates.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The liability recognized corresponds to the present value of the obligation at the consolidated balance sheet date less the fair value of plan assets. The defined benefit obligation is calculated annually by independent actuaries using the projected unit credit method. The present value of the obligation is determined by discounting the estimated future cash flows at interest rates of bonds denominated in the currency in which the benefits will be paid and with maturities similar to those of the related obligations. Actuarial gains and losses arising from changes in actuarial assumptions or differences between assumptions and reality are recognized in equity under "Other comprehensive income". Past service costs are recognized in the consolidated statement of profit and loss under "Personnel expenses".
Termination benefits are recognized on the earlier of the following dates: (a) when the Group can no longer withdraw the offer or (b) when the Group recognizes costs of a restructuring within the scope of IAS 37 and this results in the payment of termination benefits.
The Group recognizes the expected cost of short-term compensation in the form of paid leave whose rights accrue as employees render the services that entitle them to receive it.
The Group recognizes the expected cost of profit sharing or employee incentive plans when there is a present legal or constructive obligation as a result of past events and a reliable estimate can be made of the value of the obligation.
The Group has granted different incentive plans based on equity instruments to certain members of the management team who are rendering service to the company, which will be settled with equity instruments or cash, depending on the plan.
The equity instruments granted become vested when the employees complete a certain period of service and/or meet the objectives established in the incentive plan. Grifols recognizes the services received from its employees as such services are rendered during the vesting period as a personnel expense in the Consolidated Statements of Profit and Loss and a corresponding increase in equity if the transaction is equity-settled or a corresponding liability if the transaction is cash-settled, at an amount based on the value of the equity instruments.
In transactions with employees that are equity-settled, the amount recognized corresponds to the amount that will be settled once the agreed conditions are met and will not be reviewed or revalued during the vesting period, as the commitment is equity-settled. The fair value of services received is estimated by estimating the fair value of the shares granted at the grant date, net of estimated dividends to which the employee is not entitled, during the performance period.
For plans that are settled in cash, the services received and the corresponding liability are recognized at the fair value of the liability, referring to the date on which the requirements for recognition are met. Subsequently, and until settlement, the corresponding liability is measured at its fair value at the closing date of each year, with any changes in valuation occurring during the year being recognized in the Consolidated Statements of Profit and Loss. The fair value is determined by reference to the market value of the shares at the date of the estimate, net of estimated dividends to which the employee is not entitled, during the performance period.
Provisions are recognized when the Group has a present legal or constructive obligation as a result of a past event, it is probable that an outflow of resources embodying economic benefits will be required to settle the obligation and a reliable estimate can be made of the amount of the obligation. Provisions are not recognized for future operating losses.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The amount of the provision corresponds to the best estimate at the closing date of the disbursements required to settle the present obligation, after taking into account the risks and uncertainties related to the provision and, when significant, the financial effect of discounting, provided that the disbursements to be made in each period can be reliably determined.
Revenue from the sale of goods or services is recognized at an amount that reflects the consideration the Group expects to be entitled to receive in exchange for transferring goods or services to a customer, at the time the customer obtains control of the goods or services rendered, i.e. when the customer has the ability to direct the use of the goods or services. The consideration committed in a contract with a customer may include fixed amounts, variable amounts, or both. The amount of consideration may vary due to discounts, rebates, incentives, performance bonuses, penalties or other similar items. Variable consideration is only included in the transaction price when it is highly probable that the amount of revenue recognized will not be subject to significant future reversals. Revenue is presented net of value added tax and any other amounts or taxes, which in substance correspond to amounts received on behalf of third parties.
Revenue from the sale of goods is recognized when the Group satisfies the performance obligation by transferring the committed goods to the customer. A good is transferred when the customer obtains control of that asset. In assessing the satisfaction of the performance obligation, the Group considers the following indicators of the transfer of control, which include, but are not limited to, the following:
The nature of the good that the Group undertakes to transfer are mainly: sale of goods, sale of equipment, toll contracts, maintenance and technical service contracts, training, licenses, royalties and know-how and engineering contracts, among others.
In determining the transaction price, it is assumed that the goods and/or services are transferred in accordance with the terms of the contract. The consideration committed to a customer may include fixed amounts, variable amounts, or both. The price should be estimated taking into account the effect of variable consideration (as applicable) for returns, chargebacks/volume discounts or other incentives, provided that the same is highly probable.
The Group participates in state Medicaid programs in the United States. Provision for Medicaid rebates is recorded at the time the sale is recorded in an amount equal to the estimated Medicaid rebate claims attributable to such sale. The Group determines the estimate of the accrual for Medicaid rebates primarily based on historical Medicaid rebate experience, legal interpretations of applicable laws related to the Medicaid program and any new information regarding changes in Medicaid program guidelines and regulations that could affect the amount of the rebates. The Group considers pending Medicaid claims, Medicaid payments, and inventory levels in the distribution channel and adjusts the provision periodically to reflect actual experience. Although rebate payments typically occur with a lag of one to two quarters, adjustments for actual experience have not been material.
As is standard industry practice, certain customers have entered into contracts with the Group for purchases that are eligible for a price discount based on a minimum purchase quantity, volume discounts or cash discounts. These discounts are accounted for as a reduction in revenues and accounts receivable in the same month in which the revenues are recognized based on a combination of the customer's actual purchase data and historical experience when the customer's actual purchase data is later known.
In the United States, the Group enters into agreements with certain customers to establish contractual prices for goods, which these entities purchase from the authorized wholesaler or distributor (collectively, "wholesalers") of
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
their choice. Accordingly, when these entities purchase the products from the wholesalers at the contractual price which is lower than the price charged by the Group to the wholesaler, the Group provides the wholesaler with a credit known as a chargeback. The Group accounts for the accrual of chargebacks at the time of sale. The allowance account for chargebacks is based on the Group's estimate of the wholesaler's inventory levels and the expected direct sale of the products by the wholesalers at the contract price based on past chargeback history and other factors. The Group periodically monitors factors influencing the estimation for rebates and applies adjustments when it believes that actual rebates may differ from the established allowance accounts. These adjustments occur over a relatively short period of time. As these refunds are typically settled within 30 to 45 days of sale, adjustments for actual amounts have not been material.
The amount at closing for the remaining discounts is settled in the following year within 90 to 180 days depending on the type of provision.
Revenue from the rendering of services is recognized over time provided that the following criteria are met (i) the client simultaneously receives and consumes the benefits provided by Grifols' activity as it is carried out, (ii) Grifols produces or improves an asset that the client controls as the asset is produced and (iii) Grifols produces a specific asset for the client, to which cannot give an alternative use, and has an enforceable right of collection of the activity carried out so far. If the performance obligation is fulfilled over time, income is recognized as it is satisfied considering the percentage of completion. If the performance obligation does not meet the above conditions, the following indicators are evaluated to determine that control of the asset has been transferred to the client: (i) through physical possession of the asset where Grifols has the right to demand payment for it and (ii) the client has accepted the asset, the significant risks and rewards inherent in ownership of the asset and has legal title. If the performance obligation is met on a specific date, the corresponding revenue is recognized on that date.
The income tax expense or tax credit for the year comprises both current tax and deferred tax.
Current tax is the amount payable on the taxable income for the current year based on the applicable tax rate for each jurisdiction. It is calculated on the basis of the laws enacted or about to be enacted at the balance sheet date in the countries where subsidiaries and associates operate and generate taxable income. The Group periodically evaluates the positions taken in tax returns with respect to situations where the applicable tax regulations are subject to interpretation and considers such uncertainty in uncertain tax treatments when determining the corresponding tax gain or loss, tax bases, unused tax credits or tax rates.
Deferred taxes are recognized on temporary differences arising between the tax bases of assets and liabilities and their carrying amounts in the consolidated annual accounts. It is determined using tax rates (and laws) enacted or about to be enacted at the balance sheet date that are expected to apply when the related deferred tax asset is realized or the deferred tax liability is settled.
Deferred tax liabilities and assets are recognized:
• Recognition of deferred tax liabilities:
The Group recognizes deferred tax liabilities in all cases except those which:
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
• Recognition of deferred tax assets:
The Group recognizes deferred tax assets whenever:
Deferred tax assets and liabilities are not recognized for temporary differences between the carrying amount and tax base of investments in foreign operations when the company is able to control the date on which the temporary differences will reverse and it is probable that the temporary differences will not reverse in the foreseeable future. Likewise, deferred tax liabilities are not recognized if they arise from the initial recognition of goodwill. Lastly, deferred tax assets are only recognized if it is probable that sufficient future taxable profit will be available against which they can be utilized.
Deferred tax assets and liabilities are offset when there is a legally enforceable right to offset current tax assets and liabilities and when the deferred tax balances relate to the same taxation authority. Current tax assets and liabilities are offset when the entity has a legally enforceable right to offset and intends either to settle on a net basis or to realize the asset and settle the liability simultaneously.
Current or deferred income tax is recognized in profit or loss, unless it arises from a transaction or economic event that has been recognized in other comprehensive income or directly in equity. In such cases, the tax is also recognized in other comprehensive income or directly in equity, respectively.
An operating segment is a component of the Group that engages in business activities from which it may earn revenues and incur expenses, whose operating results are regularly reviewed by the Group's chief operating decision maker in order to decide on the resources to be allocated to the segment, evaluate its performance and for which discrete financial information is available.
The Group carries out operations whose main purpose is to prevent, reduce or repair damage to the environment as a result of its activities.
Items of property, plant and equipment acquired for the purpose of being used on a lasting basis in its activity and whose main purpose is the minimization of environmental impact and the protection and improvement of the environment, including the reduction or elimination of future pollution from the Group's operations, are recognized as assets through the application of measurement, presentation and disclosure criteria consistent with those mentioned in note 4(e).
The criteria for held for sale classification is regarded as met only when the Group determines the sale to be highly probable, management is committed to a decision to sell and all actions required to complete the sale indicate that it is unlikely that significant changes to the sale will be made or that the decision will be withdrawn. These assets are measured at the lower of their carrying value and fair value less costs for its alienation. Once classified as held for sale they are no longer depreciated or amortized.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
In case of having some delays caused by events or circumstances outside Grifols control and there is sufficient evidence of this commitment to sell, the Group will present those assets as held for sale despite the period for completing the sale is extended beyond one year.
The non-current assets held for sale are presented separately in the statement of financial position as "Non-current assets and disposal groups held for sale" and "Liabilities associated with non-current assets and disposal groups held for sale" for the liabilities, if exist.
Additionally, the Group considers as discontinued operations the components (cash-generating units) which represent a separate major line of business or geographic area, that is significant and can be considered separately from the rest, which are sold or disposed in an alternative way or meet the requirements to be presented as held for sale. Likewise, it is considered as discontinued operations those entities acquired exclusively with the finality to be resold. The result after taxes of these discontinued operations are presented in a separate line in the consolidated statement of profit and loss, as "Result from discontinued operations after tax".
Transactions between Group companies, except those related to mergers, spin-offs and non-cash business contributions, are recognised at the fair value of the consideration given or received. The difference between this value and the amount agreed is recognised in line with the underlying economic substance of the transaction.
In non-monetary contributions to Group companies, the contributor will value its interests at the carrying amount of the equity investments, in the consolidated financial statements at the date the transaction occurred.
Any difference between the value assigned to the interest received by the contributor and the carrying amount of the investments contributed will be recognised in reserves.
In accordance with IFRS 8 "Operating Segments", financial information for operating segments is reported in the accompanying Appendix II, which forms an integral part of this note to the consolidated annual accounts.
The definition of business segments is based on the different activities carried out by the Group and their significant importance, as well as the organizational structure for managing the businesses. It also considers how management and administrators analyze key operational and financial metrics to make decisions regarding resource allocation and to evaluate the Group's performance.
Assets, liabilities, income and expenses for segments include directly and reliably attributable items. Items which are not attributed to segments by the Group are:
The operating segments are as follows:
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Details of sales by groups of products for 2024, 2023 and 2022 are as follows:
| Thousands of Euros | ||||
|---|---|---|---|---|
| 2024 | 2023 | 2022 | ||
| Biopharma | ||||
| Haemoderivatives | 6,142,588 | 5,558,301 | 5,005,382 | |
| Diagnostic | ||||
| Transfusional medicine | 625,217 | 648,479 | 640,604 | |
| Other diagnostic | 19,681 | 21,790 | 21,740 | |
| Bio supplies | 215,664 | 159,957 | 146,076 | |
| Others | 209,232 | 203,450 | 250,165 | |
| Total | 7,212,382 | 6,591,977 | 6,063,967 |
The Group has concluded that hemoderivative products are sufficiently alike to be considered as a whole for the following reasons:
At 31 December 2024, 94,9% of the income from the sale of goods and services has been recognized at a certain point-in-time (98.0% in 2023 and 97.6% in 2022).
Geographical information is grouped into four areas:
The definition of these four segments is mainly due to the geographical level that Group management sets to manage its revenue as they respond to specific economic scenarios. The main framework of the Group is consistent with this geographical segment grouping, including the monitoring of its commercial operations and its information systems.
The financial information reported for geographical areas is based on sales to third parties in these markets as well as the location of assets.
In both 2024 and 2022 there is no customer that represents more than 10% of the Group's gross revenue. In 2023, a customer in the Biopharma segment represents approximately the 10.37% of the Group's gross revenue.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Details of and movement in this caption of the consolidated balance sheet at 31 December 2024 are as follows:
| Thousands of Euros | |||||||
|---|---|---|---|---|---|---|---|
| Balance at | Business | Translation | Balance at | ||||
| Segment | 31/12/2023 | Combination | Disposals | Impairment | differences | 31/12/2024 | |
| Net value | |||||||
| Grifols UK, Ltd. (UK) | Biopharma | 7,907 | — | — | — | 380 | 8,287 |
| Grifols Italia.S.p.A. (Italy) | Biopharma | 6,118 | — | — | — | — | 6,118 |
| Biomat USA, Inc. (USA) | Biopharma | 868,674 | — | (11,037) | — | 54,756 | 912,393 |
| Grifols Australia Pty Ltd. (Australia) / Medion Diagnostics AG (Switzerland) |
Diagnostic | 9,846 | — | — | — | (251) | 9,595 |
| Grifols Therapeutics, Inc. (USA) | Biopharma | 2,011,030 | — | — | — | 127,952 | 2,138,982 |
| Progenika Biopharma, S.A. (Spain) | Diagnostic | 40,516 | — | — | — | — | 40,516 |
| Grifols Diagnostic (Novartis & Hologic) (USA, Spain and Hong Kong) |
Diagnostic | 2,628,995 | — | — | — | 165,805 | 2,794,800 |
| Kiro Grifols, S.L. (Spain) | Others | 24,376 | — | — | (8,961) | — | 15,415 |
| Haema, AG. (Germany) | Biopharma | 190,014 | — | — | — | — | 190,014 |
| BPC Plasma, Inc. (formerly Biotest Pharma, Corp.) (USA) |
Biopharma | 155,370 | — | — | — | 9,885 | 165,255 |
| Plasmavita Healthcare GmbH (Germany) | Biopharma | 9,987 | — | — | — | — | 9,987 |
| Alkahest, Inc (USA) | Others | 79,615 | — | — | — | 5,066 | 84,681 |
| Grifols Canada Therapeutics, Inc (Canada) |
Biopharma | 152,841 | — | — | — | (3,129) | 149,712 |
| GigaGen, Inc (USA) | Others | 115,434 | — | — | — | 7,344 | 122,778 |
| Haema Plasma Kft. (Hungary) | Biopharma | 14,149 | — | — | — | (982) | 13,167 |
| Grifols Canada Plasma, Inc. (formerly Prometic Plasma Resources, Inc.) (Canada) |
Biopharma | 10,503 | — | — | — | (215) | 10,288 |
| Grifols Biotest Holdings GmbH / Biotest AG (Germany) |
Biopharma | 303,624 | — | — | — | — | 303,624 |
| Grifols Bio Supplies Inc (USA) | Bio Supplies | 173,128 | — | — | — | 11,015 | 184,143 |
| Biomat Holdings LLC (USA) | Others | — | 233,421 | — | — | 9,880 | 243,301 |
| 6,802,127 | 233,421 | (11,037) | (8,961) | 387,506 | 7,403,056 |
(See note 3)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Details of and movement in this caption of the consolidated balance sheet at 31 December 2023 were as follows:
| Thousands of Euros | |||||||
|---|---|---|---|---|---|---|---|
| Balance at | Business | Translation | Balance at | ||||
| Segment | 31/12/2022 | Combination | Disposals | Transfers | differences | 31/12/2023 | |
| Net value | |||||||
| Grifols UK, Ltd. (UK) | Biopharma | 7,747 | — | — | — | 160 | 7,907 |
| Grifols Italia.S.p.A. (Italy) | Biopharma | 6,118 | — | — | — | — | 6,118 |
| Biomat USA, Inc. (USA) | Biopharma | 899,948 | — | — | — | (31,274) | 868,674 |
| Grifols Australia Pty Ltd. (Australia) / Medion Diagnostics AG (Switzerland) |
Diagnóstico | 9,859 | — | — | — | (13) | 9,846 |
| Grifols Therapeutics, Inc. (USA) | Biopharma | 2,083,432 | — | — | — | (72,402) | 2,011,030 |
| Progenika Biopharma, S.A. (Spain) | Diagnóstico | 40,516 | — | — | — | — | 40,516 |
| Grifols Diagnostic (Novartis & Hologic) (USA, Spain and Hong Kong) |
Diagnóstico | 2,722,785 | — | — | — | (93,790) | 2,628,995 |
| Kiro Grifols, S.L. (Spain) | Otros | 24,376 | — | — | — | — | 24,376 |
| Haema, AG. (Germany) | Biopharma | 190,014 | — | — | — | — | 190,014 |
| BPC Plasma, Inc. (formerly Biotest Pharma, Corp.) (USA) |
Biopharma | 160,964 | — | — | — | (5,594) | 155,370 |
| Plasmavita Healthcare GmbH (Germany) Biopharma | 9,987 | — | — | — | — | 9,987 | |
| Alkahest, Inc (USA) | Otros | 82,481 | — | — | — | (2,866) | 79,615 |
| Grifols Canada Therapeutics, Inc (Canada) |
Biopharma | 154,775 | — | — | — | (1,934) | 152,841 |
| GigaGen, Inc (USA) | Otros | 119,590 | — | — | — | (4,156) | 115,434 |
| Haema Plasma Kft. (Hungary) | Biopharma | 13,529 | — | — | — | 620 | 14,149 |
| Grifols Canada Plasma, Inc. (formerly Prometic Plasma Resources, Inc.) (Canada) |
Biopharma | 2,802 | 7,858 | — | — | (157) | 10,503 |
| Grifols Biotest Holdings GmbH / Biotest AG (Germany) |
Biopharma | 303,624 | — | — | — | — | 303,624 |
| Access Biologicals, LLC (USA) | Bio Supplies | 179,362 | — | — | (174,427) | (4,935) | — |
| Grifols Bio Supplies Inc (USA) | Bio Supplies | — | — | — | 174,427 | (1,299) | 173,128 |
| AlbaJuna Therapeutics, S.L (Spain) | Otros | — | 1,794 | (1,794) | — | — | — |
| 7,011,909 | 9,652 | (1,794) — | (217,640) | 6,802,127 | |||
(see Note 3)
CGUs correspond to the reporting segments except for the Others segment which corresponds to Kiro Grifols, Alkahest and GigaGen as separated CGUs.
As a result of the acquisition of Talecris in 2011, and for impairment testing purposes, the Group combines the CGUs allocated to the Biopharma segment, grouping them together at segment level, because substantial synergies were expected to arise on the acquisition of Talecris, and due to the vertical integration of the business and the lack of an independent organized market for the products. Because the synergies benefit the Biopharma segment globally they cannot be allocated to individual CGUs. The Biopharma segment represents the lowest level to which goodwill is allocated and is subject to control by Group management for internal control purposes.
As a result of the acquisition of Novartis' Diagnostic business unit in 2014, the Group decided to combine Araclon, Progenika, Australia and Hologic's share of NAT donor screening unit acquisition into a single CGU for the Diagnostic business as the acquisition is supporting not only the vertically integration business but also cross-selling opportunities. In addition, for management purposes, the Group's management is focused on the business more than geographical areas or individual companies.
In addition, due to the acquisition of the remaining 51% stake in Access Biologicals LLC in the year 2022, a new CGU for the Bio Supplies business was identified (note 3).
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The CGUs established by Grifols management are:
The recoverable amount of the Biopharma CGU, Bio Supplies and Kiro Grifols CGU has been calculated based on its value in use calculated as the present value of the five-year future cash flows discounted at a discount rate considering the related inherent risk.
The recoverable amount of the Diagnostic CGU has been calculated based on its fair value less costs to sell calculated as the present value of future cash flows approved by Management discounted at a discount rate considering the inherent risk. Due to the reorganization to boost the business units, a long- term strategic plan was approved in order to transform the Diagnostic business unit by investments which will lead to a beyond five-year growth. Consequently, management has estimated future cash flows for the period 2025 – 2034.
For the calculation of the recoverable amount, management has considered:
Cash flows estimated as of the year in which stable growth in the CGU has been reached are extrapolated using the estimated growth rates indicated below. Perpetual growth rates are consistent with the forecasts included in industry reports.
The recoverable amount of the GigaGen CGU has been determined based on the fair value less costs to sell, calculated as the present value of the future cash flows mainly of a research and development project that have been approved by management, adjusted by the probability of success and discounted at a discount rate that includes their inherent risk. Cash flows have been estimated taking into consideration a useful life of 20 years from the product launch and their reduction as of the sixth year.
Alkahest's goodwill was generated as a counterpart to the deferred tax liability corresponding to the intangible assets recognized as a result of the allocation of the excess purchase price over the acquired net assets.
The recoverable amount of Alkahest CGU has been determined based on the fair value less costs to sell, calculated as the present value of the future cash flows mainly of four research and development project that have been approved by management, adjusted by the probability of success and discounted at a discount rate that includes their inherent risk. Cash flows have been estimated taking into consideration a useful life of 20 years from the product launch.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The key assumptions used in calculating impairment testing of the CGUs for 2024 have been as follows:
| Perpetual Growth rate | Pre-tax discount rate | |||
|---|---|---|---|---|
| Biopharma | 2.1% | 11.4% | ||
| Diagnostic | 2.0% | 10.6% | ||
| Bio Supplies | 1.9% | 10.6% | ||
| Kiro Grifols | 1.6% | 11.6% | ||
| GigaGen | N/A | 17.9% | ||
| Alkahest | N/A | 25,9% - 39,8% |
Additionally, the following key assumptions have been used for the GigaGen and Alkahest CGU impairment testing in 2024:
| Sink rate | Success rate | |||
|---|---|---|---|---|
| GigaGen | 5.0% | 20.0% | ||
| Alkahest | N/A | 12,0% - 17,0% |
Likewise, for the impairment test of the Diagnostic CGU in 2024, the sales of Molecular Donor Screening (MDS), Blood Typing Solution (BTS) and those of the Clinical Diagnostic (CDx) have been considered as key assumptions based on the information regarding sales and EBITDA of the CGU detailed below:
| CAGR | CAGR | CAGR | CAGR | |
|---|---|---|---|---|
| sales | sales | EBITDA | EBITDA | |
| 2024-2029 | 2029-2034 | 2024-2029 | 2029-2034 | |
| Diagnostic | 5% | 9% | 10% | 15% |
The discount rate used reflects specific risks relating to the CGUs and the countries in which they operate. The main assumptions used for determining the discount rate are as follows:
The key assumptions used in calculating impairment testing of the CGUs for 2023 were as follows:
| Perpetual Growth rate | Pre-tax discount rate | ||
|---|---|---|---|
| Biopharma | 2.0% | 11.3% | |
| Diagnostic | 2.0% | 10.1% | |
| Bio Supplies | 2.0% | 11.4% | |
| Kiro Grifols | 1.6% | 12.0% | |
| GigaGen | NA | 19.8% | |
| Alkahest | NA | 25,9% - 39,8% |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Additionally, the following key assumptions were used for the GigaGen and Alkahest CGU impairment testing in 2023:
| Sink rate | Success rate | ||
|---|---|---|---|
| GigaGen | 5.0% | 20.0% | |
| Alkahest | NA | 12,0% - 17,0% |
Likewise, for the impairment test of the Diagnostic CGU in 2023, the sales of Molecular Donor Screeing (MDS), Blood Typing Solution (BTS) and those of the Clinical Diagnostic (CDx) were considered as key assumptions.
In 2024, an impairment loss on the goodwill of the Kiro Grifols CGU was recognized for an amount of Euros 8,961 thousand.
Additionally, in 2024, the Parent Company compared the results obtained in the impairment test of the Diagnostics CGU with a report prepared by an independent third expert.
In 2024, and according to the current economic context, the reasonably possible changes considered for the CGUs impairment testing are a variation in the discount rate, as well as in the estimated perpetual growth rate, with independent movements of each other, as follows:
| Perpetual Growth rate | Pre-tax discount rate | |
|---|---|---|
| Biopharma | +/- 50 bps | +/- 50 bps |
| Diagnostic | +/- 50 bps | +/- 100 bps |
| Bio Supplies | +/- 50 bps | +/- 50 bps |
| Kiro Grifols | +/- 50 bps | +/- 50 bps |
| GigaGen | N/A | +/- 200 bps |
| Alkahest | N/A | +/- 200 bps |
Additionally, for the impairment test of the Diagnostic CGU for the year 2024, the following sensitivity scenarios to variations in sales of the MDS, BTS and CDx business lines have also been considered:
In addition, the following reasonably possible change has been considered for the GigaGen CGU impairment testing for the year 2024:
Sink rate
GigaGen +/- 100 bps
The reasonably possible changes in key assumptions considered by management in the calculation of the recoverable amount of the Biopharma and Bio Supplies CGU's would not cause the carrying amount to exceed its recoverable amount.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The reasonably possible changes in key assumptions considered by management in the calculation of the different CGU recoverable amount would cause the carrying amount to exceed its recoverable amount as follows:
| % Asset Value | |
|---|---|
| Aggregate sensitivity scenario to MDS, BTS and CDx sales | -10% |
| Discount rate sensitivity GigaGen +200 bps | -7% |
| Discount rate sensitivity Alkahest +200 bps | -17% |
| Discount rate sensitivity Kiro +50 bps | -5% |
| Perpetual growth rate Kiro -50 bps | -4% |
Detail of the assets by segment value is shown in Appendix II.
In 2023, the reasonably possible changes considered for the Diagnostic CGUs impairment testing were a variation in the discount rate, as well as in the estimated perpetual growth rate, with independent movements of each other, as follows:
| Perpetual Growth rate | Pre-tax discount rate | ||
|---|---|---|---|
| Biopharma | +/- 50 bps | +/- 50 bps | |
| Diagnostic | +/- 50 bps | +/- 100 bps | |
| Bio Supplies | +/- 50 bps | +/- 50 bps | |
| Kiro Grifols | +/- 50 bps | +/- 50 bps | |
| GigaGen | N/A | +/- 200 bps |
Additionally, for the impairment test of the Diagnostic CGU for the year 2023, the following sensitivity scenarios to variations in sales of the MDS, BTS and CDx business lines were also considered:
In addition, the following reasonably possible change for the year 2023 was considered for the GigaGen CGU impairment testing:
Sink rate
GigaGen +/- 100 bps
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Details of other intangible assets and movement during the years ended 31 December 2024 and 2023 are included in Appendix III, which forms an integral part of these notes to the consolidated annual accounts.
Intangible assets acquired from Talecris mainly include currently marketed products. Identifiable intangible assets correspond to Gamunex and have been recognized at fair value at the acquisition date of Talecris and classified as currently marketed products. Intangible assets recognized comprise the rights on the Gamunex product, its commercialization and distribution license, trademark, as well as relations with hospitals. Each of these components is closely linked and fully complementary, are subject to similar risks and have a similar regulatory approval process.
Intangible assets acquired from Progenika mainly include currently marketed products. Identifiable intangible assets correspond to blood, immunology and cardiovascular genotyping. These assets have been recognized at fair value at the acquisition date of Progenika and classified as currently marketed products.
The intangible assets acquired from Biotest mainly include the acquired product portfolio. The identifiable intangible assets correspond to the plasma therapies segment and have been recorded at fair value at the date of acquisition of Biotest and classified as an acquired product portfolio.
The intangible assets acquired from Access Biologicals LLC mainly include customer relationships. This asset has been recorded at fair value at the date of acquisition of Access Biologicals LLC and classified as acquired customer relationships.
The estimated useful life of the currently marketed products acquired from Talecris is considered limited, has been estimated at 30 years on the basis of the expected life cycle of the product (Gamunex) and is amortized on a straightline basis.
At 31 December 2024, the residual useful life of currently marketed products is 16 years and 5 months (17 years and 5 months at 31 December 2023).
The estimated useful life of the currently marketed products acquired from Progenika is considered limited, has been estimated at 10 years on the basis of the expected life cycle of the product and is amortized on a straight-line basis. In 2023 the currently marketed products reached the end of their useful life.
The estimated useful life of the product portfolio acquired from Biotest is considered limited and has been estimated at 30 years, based on the expected life cycle of the products. The amortization method is linear.
The estimated useful life of the customer relationships acquired from Access Biologicals LLC is considered limited and has been estimated at 14 years, based on the rate of decline of the same. The amortization method is linear.
At 31 December 2024 the Group has recognized Euros 106,902 thousand as self – constructed intangible assets (Euros 50,043 thousand at 31 December 2023) in the consolidated profit and loss account.
At 31 December 2024 and 2023, the Group does not have any significant intangible purchase commitments.
At 31 December 2024, the Group has an amount of Euros 1,471,975 thousand as development costs in progress (Euros 1,366,893 thousand at 31 December 2023). This amount includes an amount of Euros 302,433 thousand as of 31 December 2024 (Euros 284,341 thousand as of 31 December 2023) corresponding to the ongoing research and development projects for products for neurodegenerative disorders, neuromuscular diseases, and ophthalmological diseases acquired from Alkahest. Likewise, this amount also includes an amount of Euros 878,872 thousand as of 31 December 2024 (Euros 861,950 thousand as of 31 December 2023)corresponding to the ongoing research and development projects in plasma therapies acquired from Biotest (Fibrinogen and Trimodulin).
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The total losses on disposals and sale of intangible assets amounts to Euros 144 thousand in 2024 (losses of Euros 283 thousand in 2023).
Indefinite-lived intangible assets have been allocated to the corresponding cash-generating unit (CGU). These assets have been tested for impairment together with goodwill (see note 6).
Impairment testing has been analyzed for each of the intangible assets in progress by calculating its recoverable amount based on their fair value based on the discount of free cash flows adjusted by the probability of success according to the clinical phase of the project.
Details of leases in the consolidated balance sheet at 31 December 2024 and 2023 are as follows:
| Right-of-use assets | Thousands of Euros | |
|---|---|---|
| 31/12/2024 | 31/12/2023 | |
| Land and buildings | 956,617 | 933,304 |
| Machinery | 3,173 | 3,718 |
| Computer equipment | 1,032 | 764 |
| Vehicles | 7,482 | 7,454 |
| 968,304 | 945,240 |
| Lease liabilities | Thousands of Euros | ||
|---|---|---|---|
| Reference | 31/12/2024 | 31/12/2023 | |
| Non-current | Note 21 | 1,024,845 | 1,004,227 |
| Current | Note 21 | 116,534 | 107,101 |
| 1,141,379 | 1,111,328 |
The composition of lease liabilities as of 31 December 2024 and 2023 is shown below. Undiscounted future payments classified on a maturity basis are presented together with the effect of the financial discount:
| Thousands of Euros | |||
|---|---|---|---|
| 31/12/2024 | 31/12/2023 | ||
| Maturity: | |||
| Within one year | 116,534 | 107,101 | |
| In the second year | 117,233 | 126,133 | |
| In the third to fifth years | 319,410 | 326,253 | |
| After the fifth year | 1,221,344 | 1,003,424 | |
| 1,774,521 | 1,562,911 | ||
| Discounting effect | (633,142) | (451,581) | |
| Total lease liabilities | 1,141,379 | 1,111,328 | |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
At 31 December 2024, the Group has recognized an amount of Euros 79,051 thousand related to additions of right-ofuse assets (Euros 102,904 thousand at 31 December 2023). Movement at 31 December 2024 and 2023 is included in Appendix IV, which forms an integral part of these notes to the consolidated annual accounts.
At 31 December 2024 and 2023, the amounts recognized in the consolidated statement of profit and loss related to lease agreements are:
| Right-of-use depreciation | Thousands of Euros | ||
|---|---|---|---|
| 2024 | 2023 | ||
| Buildings | 74,929 | 71,157 | |
| Machinery | 1,522 | 1,507 | |
| Computer equipment | 559 | 860 | |
| Vehicles | 5,106 | 5,019 | |
| 82,116 | 78,543 |
| Thousands of Euros | ||||
|---|---|---|---|---|
| Reference | 2024 | 2023 | ||
| Finance lease expenses | Note 27 | 50,870 | 44,587 | |
| 50,870 | 44,587 |
| Thousands of Euros | |||
|---|---|---|---|
| 2024 | 2023 | ||
| Expenses related to short-term contracts | 1,295 | 1,739 | |
| Expenses related to low-value contracts | 15,865 | 13,435 | |
| Other operating lease expenses | 30,101 | 23,820 | |
| 47,261 | 38,994 |
At 31 December 2024, the Group has paid a total of Euros 111,488 thousand related to lease contracts (Euros 116,394 thousand at 31 December 2023).
The total amount recognized in the consolidated balance sheet corresponds to lease contracts in which the Group is the lessee.
Details of property, plant and equipment and movement in the consolidated balance sheet at 31 December 2024 and 2023 are included in Appendix V, which forms an integral part of this note to the consolidated annual accounts.
Property, plant and development under construction at 31 December 2024 and 2023, mainly comprise investments made to extend the companies' equipment and to increase their productive capacity.
In 2024 the Group has capitalized interests for a total amount of Euros 27,772 thousand (Euros 36,892 thousand in 2023) (note 27).
Group policy is to contract sufficient insurance coverage for the risk of damage to property, plant and equipment. At 31 December 2024, the Group has a combined insurance policy for all Group companies, which more than adequately covers the carrying amount of all the Group's assets.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Total losses incurred on disposals of property, plant and equipment for 2024 amount to Euros 3,465 thousand (losses of Euros 5,813 thousand in 2023).
At 31 December 2024 the Group has recognized Euros 62,638 thousand as self -constructed property, plant and equipment (Euros 82,615 thousand at 31 December 2023) in the Consolidated Statements of Profit and Loss.
At 31 December 2024, the Group has property, plant and equipment purchase commitments amounting to Euros 35,009 thousand (Euros 36,487 thousand at 31 December 2023).
Property, plant and equipment under construction as of 31 December 2024 amount to Euros 802,313 thousand (Euros 910,671 thousand in the 2023) and mainly correspond to the investments incurred in the expansion of the facilities of the companies and their productive capacity in the United States, Canada, and Ireland (note 29).
As of December 31, 2024, the Group has recognized an impairment loss amounting to Euros 1,370 thousand.
During 2023 the Group disposed property, plant and equipment as part of the reorganization of the USA donor center network. In this regard, the impairment corresponding to these assets which belong to the Biopharma segment was written off for a total amount of Euros 5.3 million.
Details of this caption in the consolidated balance sheet at 31 December 2024 and 2023 are as follows:
| Thousands of Euros |
Thousands of Euros |
|||
|---|---|---|---|---|
| % ownership (*) |
31/12/2024 | % ownership (*) |
31/12/2023 (') | |
| Shanghai RAAS Blood Products Co., Ltd. | — % | — | 6.58 % | 361,394 |
| Grifols Egypt Plasma Derivatives | 49.00 % | 63,063 | 49.00 % | 46,263 |
| BioDarou P.J.S. Co. | 49.00 % | 5,933 | 49.00 % | 11,265 |
| Total equity accounted investees with similar activity to that of the Group |
68,996 | 418,922 | ||
| Mecwins, S.A. | — % | — | 24.59 % | 2,841 |
| Total of the rest of equity accounted investees | — | 2,841 | ||
| Total equity-accounted investees | 68,996 | 421,763 | ||
(*) This percentage also refers to the voting interest. (') Restated figures (Note 2.d.)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Movement in the investments in equity-accounted investees for the year ended 31 December 2024 is as follows:
| Thousands of Euros | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| 2024 | |||||||||
| Equity accounted investees with similar activity to that of the Group | Rest of equity accounted investees | ||||||||
| Shanghai RAAS Blood Products Co., Ltd. |
Grifols Egypt Plasma Derivatives |
BioDarou P.J.S. Co. |
Total | Mecwins, S.A. | Total | Total | |||
| Balance at 1 January (*) | 361,394 | 46,263 | 11,265 | 418,922 | 2,841 | 2,841 | 421,763 | ||
| — | — | ||||||||
| Acquisitions | — | 40,250 | — | 40,250 | — | — | 40,250 | ||
| Share of profit / (losses) | 12,595 | 333 | (4,388) | 8,540 | — | — | 8,540 | ||
| Share of other comprehensive income / translation differences |
435 | (23,783) | 4,882 | (18,466) | — | — | (18,466) | ||
| Collected dividends | (6,724) | — | — | (6,724) | — | — | (6,724) | ||
| Impairment loss | — | — | (5,826) | (5,826) | — | — | (5,826) | ||
| Transfers | (367,700) | — | — | (367,700) | (2,841) | (2,841) | (370,541) | ||
| Balance at 31 December | — | 63,063 | 5,933 | 68,996 | — | — | 68,996 | ||
(*) Restated figures (Note 2.d.)
Additionally, as a result of the sale of SRAAS (note 12), an operating profit of Euros 34,090 thousand has been generated, which has been recorded under the heading 'Profit of equity accounted investees with similar activity to that of the Group' in the attached Consolidated Statements of Profit and Loss.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Movement in the investments in equity-accounted investees for the year ended 31 December 2023 is as follows:
| 2023 | ||||||||
|---|---|---|---|---|---|---|---|---|
| Equity accounted investees with similar activity to that of the Group | Rest of equity accounted investees | |||||||
| Shanghai RAAS Blood Products Co., Ltd. |
Grifols Egypt Plasma Derivatives |
BioDarou P.J.S. Co. |
Total | Albajuna Therapeutics, S.L. |
Mecwins, S.A. | Total | Total | |
| Balance at 1 January (*) | 1,453,210 | 36,111 | 5,051 | 1,494,372 | 622 | 2,965 | 3,587 | 1,497,959 |
| Acquisitions | — — |
— 20,342 |
— | 20,342 | — | — | — | 20,342 |
| Share of profit / (losses) | 61,979 | (1,025) | 2,786 | 63,740 | (798) | (124) | (922) | 62,818 |
| Share of other comprehensive income / translation differences (1) |
(57,048) | (9,165) | 3,846 | (62,367) | 176 | — | 176 | (62,191) |
| Collected dividends | (6,891) | — | — | (6,891) | — | — | — | (6,891) |
| Uncollected dividends | — | — | (418) | (418) | — | — | — | (418) |
| Transfers (*) | (1,089,856) | — | — | (1,089,856) | — | — | — | (1,089,856) |
| — | — | — | — | — | — | — | — | |
| Balance at 31 December (*) | 361,394 | 46,263 | 11,265 | 418,922 | — | 2,841 | 2,841 | 421,763 |
(*) Restated figures (Note 2.d.)
(1) Due to an imprecision in the sign of the subheading "Equity accounted investees / Translation differences" of the Consolidated Statement of Comprehensive Income for the years 2023 and 2022, in the current financial year the sign of this caption has been modified, with the counterpart item being the subheading "Translation differences", of the consolidated Statement of Comprehensive Income.
As a result of this imprecision, this subheading has been modified for the amount of Euros 124 million and Euros 61 million as of December 31, 2023 and 2022, respectively, against the subheading "Participation in other comprehensive income of the investments accounted for by the equity method - Translation differences". This imprecision has not had any impact on the total heading "Translation differences" considered globally in the Consolidated Balance Sheet.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Movement in the investments in equity-accounted investees for the year ended 31 December 2022 s as follows:
| Thousands of Euros | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| 2022 | |||||||||
| Equity accounted investees with similar activity to that of the Group | Rest of equity accounted investees | ||||||||
| Access Biologicals LLC |
Shanghai RAAS Blood Products Co., Ltd. |
Grifols Egypt Plasma Derivatives |
BioDarou P.J.S. Co. |
Total | Albajuna Therapeutics, S.L |
Mecwins, S.A. |
Total | Total | |
| Balance at 1 January (*) | 53,264 | 1,452,378 | 31,847 | — | 1,537,489 | 1,910 | 3,159 | 5,069 | 1,542,558 |
| Acquisitions | — | — | — | 4,534 | 4,534 | — | — | — | 4,534 |
| Transfers | (129,459) | — | — | — | (129,459) | — | — | — | (129,459) |
| Share of profit / (losses) | 76,895 | 26,680 | 865 | (962) | 103,478 | (1,288) | (194) | (1,482) | 101,996 |
| Share of other comprehensive income / translation differences |
3,028 | (18,859) | (16,419) | 1,479 | (30,771) | — | — | — | (30,771) |
| Collected dividends | (3,728) | (6,989) | — | — | (10,717) | — | — | — | (10,717) |
| Others | — | — | 19,818 | — | 19,818 | — | — | — | 19,818 |
| Balance at 31 December (*) | — | 1,453,210 | 36,111 | 5,051 | 1,494,372 | 622 | 2,965 | 3,587 | 1,497,959 |
(*) Restated figures (Note 2.d.)
(1) Due to an imprecision in the sign of the subheading "Equity accounted investees / Translation differences" of the Consolidated Statement of Comprehensive Income for the years 2023 and 2022, in the current financial year the sign of this caption has been modified, with the counterpart item being the subheading "Translation differences", of the consolidated Statement of Comprehensive Income.
As a result of this imprecision, this subheading has been modified for the amount of Euros 124 million and Euros 61 million as of December 31, 2023 and 2022, respectively, against the subheading "Participation in other comprehensive income of the investments accounted for by the equity method - Translation differences". This imprecision has not had any impact on the total heading "Translation differences" considered globally in the Consolidated Balance Sheet.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The main movements of the equity-accounted investees with similar activity to that of the Group are explained below:
On 29 July 2021, a cooperation agreement was signed with the National Service Projects Organization (NSPO) to help build a platform to bring self-sufficiency in plasma-derived medicines to Egypt. The Company made a first contribution of US Dollars 36,750 thousand (equivalent to Euros 30,454 thousand at the date of integration), and in exchange received Grifols Egypt for Plasma Derivatives (S.A.E.) shares representing 49% of its share capital, which will amount to US Dollars 300 million. The Company has undertaken to make the contributions for the outstanding amount corresponding to its interest as the capital requirements are approved. As a result, the Group made a further capital contribution of US Dollars 44,100 thousand during 2024 (US Dollars 22,050 and 22,050 thousand in 2023 and 2022, respectively), equivalent to 49% of the total capital capital increase made of US Dollars 90 million (US Dollars 45 and 45 million in 2023 and 2022, respectively). Thus, the total contributions made by the Group amount to US Dollars 124,950 thousand, equivalent to 49% of its share capital, which total amount is US Dollar 255 millions. Additionally, the Group has committed to make a capital contribution of US Dollars 22,050 thousand during the second quarter of 2025.
On December 29, 2023, Grifols reached an agreement with Haier for the sale of a 20% shareholding subject to regulatory approvals and other conditions agreed in the agreement. As a result of the Share Purchase Agreement, at December 31, 2023 the amount equivalent to 20% of the shareholding in SRAAS was reclassified to Non-current assets held for sale for Euros 1,089,856 thousand (note 12).
According to the fair value implicit in the transaction with Haier, there was no impairment indication in SRAAS investment as of 31 December 2023. At 31 December 2023 Shanghai RAAS Blood Products Co. Ltd. stock market capitalization totaled RMB 53,164 million (RMB 42,737 million at 31 December 2022).
| Agreed price in transaction with Haier |
31/12/2023 | Date of acquisition | |
|---|---|---|---|
| SRAAS shares price | CNY 9.405 | CNY 8.00 | CNY 7.91 |
On June 18, 2024 the sale transaction was closed and Grifols loses its significant influence over its interest in SRAAS at the closing of the transaction. The remaining 6.58% interest in the shares of SRAAS is considered a financial asset measured at fair value through "Other comprehensive income" at the transaction date and has been reclassified to financial asset (note 11 and 12).
On 12 January 2017, the group announced the acquisition of 49% of the voting rights in Access Biologicals LLC, a company based in San Diego, California, USA, for the amount of US Dollars 51 million. Grifols entered into an option agreement to purchase the remaining 51% voting rights in five years, in 2022. Grifols also signed a supply agreement to sell biological products not meant for therapeutic use to Access Biologicals LLC.
The principal business activity of Access Biologicals LLC is the collection and manufacturing of an extensive portfolio of biological products. Combined with closed-loop material sourcing, it provides critical support for various markets such as in-vitro diagnostic manufacturing, biopharmaceutical, cell culture and diagnostic research and development.
On 15 June 2022, Grifols, through its wholly-owned subsidiary Chiquito Acquisition Corp., reached an agreement to acquire all the shares of Access Biologicals LLC, exercising the call option for the remaining 51%, for a total of US Dollars 142 million. With the acquisition of 100% of the shares, Grifols obtained control over Access Biologicals LLC and, therefore, it was considered a Group company and is consolidated under the full consolidation method (note 3). In 2023, all wholly-owned subsidiaries Access Biologicals, LLC, Chiquito Acquisition Corp. and Grifols Bio Supplies, Inc. entered into a merger agreement, with the surviving company being Grifols Bio Supplies, Inc. (note 2).
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
On 25 April 2022, and after obtaining all regulatory approvals, Grifols closed the acquisition of 70.18% of the share capital of Biotest AG for Euros 1,460,853 thousand (note 3). Biotest AG is the parent company of a consolidated group of companies, which includes a joint venture investment corresponding to a 49% interest held by Biotest Pharma GmbH in BioDarou P.J.S. Co, whose registered office is in Tehran, Iran, and which is accounted for using the equity method.
The company's goal is to collect plasma, process it into immunoglobulins, factors and human albumin through Biotest AG and then sell the finished products in Iran.
In 2016, Grifols made a capital investment of Euros 3.75 million in exchange for 30% of the shares of Albajuna Therapeutics, S.L. Since 2018, as a result of a planned investment in accordance with the Shareholders' Agreement of January 2016, Grifols held a 49% stake in the company's capital. Albajuna Therapeutics, S.L. is a Spanish research company founded in 2016 which main activity is the development and manufacture of therapeutic antibodies against HIV.
On 9 October, 2023, Grifols, through its 100% owned subsidiary Grifols Innovation and New Technologies Limited, reached an agreement to acquire all the shares of Albajuna Therapeutics, S.L. for the remaining 51% for a total amount of Euro 1. With the acquisition of 100% of the shares, Grifols obtained control over Albajuna Therapeutics, S.L. and, therefore, it has become a group company and is consolidated (note 3).
In February 2019, the Group completed the acquisition of 45% of the shares in Medcom Advance, S.A. for an amount of Euros 8,602 thousand. Medcom Advance, S.A. is a company dedicated to research and development with a view to create proprietary patents using nanotechnology. The company was equity-accounted. At 31 December 2023 and 2024, this investment is fully impaired.
On 22 October 2018 Grifols allocated Euros 2 million to the capital increase of Mecwins through Progenika Biopharma, reaching 24.99% of the total capital.
Mecwins is a spin-off of the Institute of Micro and Nanotechnology of the Center for Scientific Research (CSIC), specialized in the development of innovative nanotechnological analysis tools for the diagnosis and prognosis of diseases.
Mecwins has developed ultrasensitive optical reading immunoassay technology from nanosensors for the detection of protein biomarkers in blood. This technology has potential applications in fields such as oncology, cardiovascular and infectious diseases.
The injection of capital, in which CRB Inverbio also participated with an additional Euros 2 million, will enable Mecwins to start developing pre-commercial prototypes of this technology and for Grifols to position itself in the field of nanotechnology applied to diagnosis.
In 2021, Mecwins, S.A. acquired own shares from Progenika Biopharma, S.A. to generate treasury stock. This acquisition caused the percentage of ownership in Mecwins, S.A. to decrease to 24.59%.
As of December 31, 2023, the company maintained the investment accounted for using the equity method. As of December 31, 2024, since the group ceased to exercise significant influence because it no longer had representation on the Board of Directors and could not intervene in financial policy decisions or its operation, the investment has been reclassified as a financial asset with changes in "Other Comprehensive Income" (note 11).
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The most recent financial statements available of the main equity-accounted investments of Grifols are as follows:
| Balance sheet: | Thousands of Euros | |||||
|---|---|---|---|---|---|---|
| 31/12/2024 | 31/12/2023 | |||||
| Grifols Egypt Plasma Derivatives |
Shanghai RAAS Blood Products Co. Ltd. |
Grifols Egypt Plasma Derivatives |
||||
| Non-current assets | 71,167 | 2,990,702 | 74,169 | |||
| Current assets | 64,680 | 561,804 | 28,131 | |||
| Cash and cash equivalents | 47,993 | 512,309 | 36,947 | |||
| Non-current liabilities | (1,296) | (2,182) | (1,996) | |||
| Non-current financial liabilities | (8,048) | (211) | (11,044) | |||
| Current liabilities | (45,796) | (263,827) | (31,793) | |||
| Net assets | 128,700 | 3,798,595 | 94,414 |
| P&L: | Thousands of Euros | ||||
|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | |||
| Grifols Egypt Plasma Derivatives |
Shanghai RAAS Blood Products Co. Ltd. |
Grifols Egypt Plasma Derivatives |
Shanghai RAAS Blood Products Co. Ltd. |
Grifols Egypt Plasma Derivatives |
|
| Net revenue | 13,941 | 778,328 | 196 | 700,831 | — |
| Net profit | (2,318) | 234,416 | (4,423) | 227,000 | 3,397 |
Joint arrangement:
Grifols entered into a collaboration agreement with ImmunoTek GH, LLC (ImmunoTek) for the opening and management of 28 plasma collection centers. The transaction was executed through the creation of Biotek America LLC ("ITK JV"), which created a series of shares for each center (silos). Grifols holds 75% of each series of shares, and ImmunoTek holds the remaining 25%. Approximately three years after the opening of each center, according to the agreement, Grifols acquires the collection center. As of December 31, 2024, Grifols has acquired 14 plasma centers (see note 3.a.).
The collaboration agreement between the Group and Immunotek has involved, as of December 31, 2024 and 2023:
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The amounts payable net of deposits and on the basis of a minimum production and existence of the centers at the time of purchase, would be the following amounts according to the estimated payment schedule:
| Thousand | |||
|---|---|---|---|
| US Dollar | Euros | ||
| 2025 | 78,888 | 75,131 | |
| 2026 | 62,428 | 59,455 | |
| Total | 141,316 | 134,586 |
Regardless of whether Grifols holds a 75% stake and whether the management has been transferred to ImmunoTek, there is joint control until Grifols acquires the centers and will be accounted for as a joint operation based on the contractual conditions: (i) joint decision-making power on the relevant activities; (ii) Grifols' exposure to the 75% stake, the advances paid, the guarantees granted and the contracts for the purchase of plasma supply; (iii) significant exposure of the other shareholder to the results of the silos generated and their fees, given that it does not act with delegated power and, (iv) relation between the two.
Therefore, to the extent that there is joint control and each series is representative of a SILO and has been designed and created to sell all the plasma collected to Grifols and advances the necessary funds for the development of the series and guarantees the obligations, they should be considered joint agreements. However, there is a disproportion between Grifols' percentage stake in the series, which amounts to 75%, and the economic exposure to assets and liabilities of 100%, while the income and expenses and tax benefits derived therefrom from the period prior to the acquisition must be attributed to ImmunoTek. As a result, the losses generated by the series during the period prior to the acquisition belong to the other shareholder under the tax transparency regime.
As described in Note 2d), the series has been integrated in accordance with IFRS 11 Joint Arrangements, with the comparative figures for 2023 and 2022 restated accordingly.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Below is a breakdown of the aggregate balances of the 14 centers as of 31 December 2024 and 28 centers as of 31 December 2023, excluding balances with Grifols:
| Thousands of | ||||
|---|---|---|---|---|
| US Dollars | Euros | |||
| 31/12/2024 | 31/12/2023 | 31/12/2024 | 31/12/2023 | |
| Non-current assets | 54,309 | 120,133 | 52,275 | 108,718 |
| Current assets | 26,623 | 46,877 | 25,626 | 42,423 |
| Total assets | 80,932 | 167,010 | 77,901 | 151,141 |
| Non-current liabilities | 55,674 | 119,449 | 53,589 | 108,099 |
| Current liabilities | 46,759 | 71,706 | 45,008 | 64,892 |
| Total liabilities | 102,433 | 191,155 | 98,597 | 172,991 |
| Grifols' balances | 5,965 | 12,556 | 5,742 | 11,363 |
| Total Equity | (21,501) | (36,701) | (20,696) | (33,213) |
| Thousands of | ||||
| US Dollars | Euros | |||
| 2024 | 2023 | 2024 | 2023 | |
| Net revenue | 206,125 | 271,693 | 189,957 | 251,805 |
Details of non-current financial assets on the consolidated balance sheet at 31 December 2024 and 2023 are as follows:
Net profit 6,248 (18,453) 5,743 (16,997)
| Thousands of Euros | |||
|---|---|---|---|
| Reference | 31/12/2024 | 31/12/2023 | |
| Other non-current investments | 422,258 | 11,139 | |
| Non-current derivatives | Note 30 | 1,181 | 1,043 |
| Total Non-current financial assets measured at fair value | 423,439 | 12,182 | |
| Non-current guarantee deposits | 9,420 | 8,872 | |
| Other non-current financial assets | (a) | 37,718 | 18,996 |
| Non-current loans | (b) | 19,915 | 136,626 |
| Total Non-current financial assets measured at amortized cost | 67,053 | 164,494 |
In Non-current guarantee deposits, there are long-term deposits with related parties that amount Euros 943 thousand at 31 December 2024 (Euros 934 thousand at 31 December 2023) (note 31).
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The remaining 6.58% interest in SRAAS shares is included under "Other non-current investments". This investment has been considered a financial asset measured at fair value with changes in 'Other Comprehensive Income of financial investments' whose fair value at December 31, 2024 has been calculated on the basis of the SRAAS share price at that date (CNY 7.22 per share) in the amount of Euros 416,131 thousand recognizing a loss under the heading of other comprehensive income of Euros 18,351 thousand net of tax.
Details of current financial assets on the consolidated balance sheet at 31 December 2024 and 2023 are as follows:
| Thousands of Euros | |||
|---|---|---|---|
| Reference | 31/12/2024 | 31/12/2023 | |
| Current derivatives | Note 31 | 6,064 | 23,644 |
| Total Non-current financial assets measured at fair value | 6,064 | 23,644 | |
| Thousands of Euros | |||
| Reference | 31/12/2024 | 31/12/2023 | |
| Deposits and guarantees | 3,000 | 325 | |
| Other current financial assets | (a) | 21,179 | 14,926 |
| Current loans | (b) | 213,331 | 101,337 |
| Total other current financial assets measured at amortized cost | 237,510 | 116,588 |
Details of other non-current and current financial assets are as follows:
| Thousands of Euros | ||||
|---|---|---|---|---|
| Reference | 31/12/2024 | 31/12/2023 | ||
| Other financial assets with associated parties | Note 31 | 418 | 418 | |
| Other financial assets with third parties | 58,479 | 33,504 | ||
| Total other non-current and current financial assets | 58,897 | 33,922 |
Details of non-current and current loans are as follows:
| Thousands of Euros | |||
|---|---|---|---|
| Reference | 31/12/2024 | 31/12/2023 | |
| Loans to related parties | Note 31 | 214,119 | 216,426 |
| Loans to third parties | 19,127 | 21,537 | |
| Total current and non-current loans | 233,246 | 237,963 |
"Loans to related parties" includes by an amount of Euros 82,255 thousand (Euros 101,217 thousand as of 31 December 2023) the open balance of the cash pooling that Haema GmbH and BPC Plasma, Inc. have with Scranton Plasma B.V. (note 31). Despite their maturity date being 2027, these have been maintained in the short term as their recovery is expected through the collection of dividends in the coming year. Both in 2024 and 2023, BPC Plasma Inc. distributed to its shareholder Scranton Plasma B.V. a dividend without cash outflow compensating "Loans to related parties". In 2024 the dividend amounted Euros 39,509 thousand, being the dividend distributed in 2023 the result of the previous 4 years for a value of Euros 266,406 thousand. This distribution had an impact against the Group's noncontrolling interests reserves (see note 19). Furthermore, through the execution of a quota transfer agreement on 31 October 2024, Grifols Worldwide Operations Limited ("GWWO") as purchaser, acquired 100% of the share capital of Haema Plasma Kft, from Scranton Plasma B.V., as seller (the "SPA"), all of which in exchange of Euros 35,000 thousand (the "Purchase Price"). The Purchase Price has been paid by GWWO to Scranton Plasma B.V. through the
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
partial assignment by GWWO to Scranton Plasma B.V. of part of certain receivable held by GWWO against Haema GmbH (under certain advance payment made in the past by GWWO to Haema GmbH for the purchase of plasma (the "Plasma Advance Receivable")) in the amount of the Purchase Price (the "Assigned Receivable"). Now therefore, the amount of the Plasma Advance Receivable has been reduced in the amount of the Assigned Receivable. In turn and in addition, upon receipt by Scranton Plasma B.V. of the Assigned Receivable, Scranton Plasma B.V., as creditor under the Assigned Receivable against Haema GmbH, as debtor thereunder, has settled its debt position under the cashpooling financing agreement in the amount of the Assigned Receivable (and hence, the amount outstanding under the cash-pooling arrangement between Haema GmbH, as creditor and Scranton Plasma B.V., as debtor, has been reduced in the amount of the Assigned Receivable).
Additionally, this caption includes the loan granted to Scranton Enterprises BV by the Group related to the payment of the sale of the shares of BPC Plasma, Inc. and Haema, GmbH (note 31). The initial amount of the loan was US Dollars 95,000 thousand (Euros 86,969 thousand). Furthermore, in 2023 an additional amount of Euros 15,000 thousand was drawn under the same terms as the original loan. As of 31 December 2024, the recorded amount stands at Euros 131,864 thousand, including accrued and capitalized interest to date (Euros 115,209 thousand as of 31 December 2023).
On December 29, 2023, Grifols reached an agreement with Haier Group Corporation for the sale of a 20% equity interest in Shanghai RAAS (SRAAS) for RMB 12,500,000 thousand. Pursuant to IFRS 5, such stake subject to the sale transaction was considered as a "Non-current asset held for sale" in the consolidated statement of financial position as at December 31, 2023 in the amount of Euro 1,089,856 thousand.
On June 18, 2024, after obtaining the necessary authorizations from the required regulatory authorities and fulfilling certain agreed-upon conditions, the sale took place for an amount of RMB 12,163,730 thousand, net of taxes paid in China (Euros 1,564,256 thousand at the exchange rate on the transaction date). To reduce exposure to EUR/RMB exchange rate fluctuations and ensure the amount received in euros, Grifols contracted a EUR/RMB forward exchange rate financial instrument (Fx Forward), which was not recorded as hedge accounting.
On July 5, 2024, these funds were deposited into a Grifols Euro bank account, amounting to Euros 1,559,943 thousand at the contracted Forward exchange rate, recognizing a foreign exchange loss of Euros 17,790 thousand, presented under the heading 'Foreign Exchange Differences,' and a financial gain from the derivative of Euro 13,476 thousand, recognized under the heading 'Fair Value Change in Financial Instruments' (note 27). These funds have been used to reduce the Group's debt (note 21).
As a result of this sale transaction, Grifols loses its significant influence over its interest in SRAAS at the closing of the transaction. The remaining 6.58% stake in SRAAS shares is considered a financial asset valued at fair value with changes in "FV through OCI" which fair value at the date of the transaction was calculated on the basis of the listed price of the SRAAS share at that date in the amount of Euros 434,481 thousand (note 11). Grifols also lost its indirect stake in GDS which was held through its shareholding in SRAAS, resulting in an increase of Euros 507,803 thousand in equity attributable to minority interests. In addition, as part of the transaction, a series of agreements were signed (note 29), including the extension of the exclusive distribution agreement for albumin.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
This transaction has not had a material impact on the Consolidated Statements of Profit and Loss for 2024 and is calculated as follows:
| Thousands of euros |
|
|---|---|
| Selling price | 1,607,500 |
| Fair value of SRAAS 6,58% | 434,481 |
| Minus: book value of the Non-current asset held for sale and transaction costs | (1,123,588) |
| Minus: book value of the Investment accounted for using the equity method as the date of loss of the significant influence |
(367,700) |
| Minus:increase of the minority interest of GDS (see Note 19) | (507,803) |
| Other contractual obligations (see Note 32) | (10,433) |
| Result before the reclassification of translation differences | 32,457 |
| Accumulated translation differences in equity | 1,633 |
| Transaction result:profit | 34,090 |
| Taxes on profits in China and Spain | (34,544) |
| Result net of taxes | (454) |
The result of the transaction includes an unrealized gain corresponding to the revaluation of the investment retained by Grifols in SRAAS at fair value in the amount of Euros 68,414 thousand.
Details of inventories at 31 December 2024 and 2023 are as follows:
| Thousands of Euros | ||
|---|---|---|
| 31/12/2024 | 31/12/2023 (*) | |
| Goods for resale | 164,624 | 167,894 |
| Raw materials and supplies | 955,503 | 1,092,301 |
| Work in progress and semi-finished goods | 1,405,231 | 1,210,085 |
| Finished goods | 1,034,740 | 1,012,119 |
| 3,560,098 | 3,482,399 |
(*) Restated figures (Note 2.d)
Movement in the inventory provision was as follows:
| Thousands of Euros | |||
|---|---|---|---|
| 31/12/2024 | 31/12/2023 | 31/12/2022 | |
| Balance at 1 January | 123,656 | 84,740 | 158,724 |
| Net charge for the year | 22,711 | 57,041 | (66,647) |
| Cancellations for the year | (133) | (15,985) | (12,155) |
| Translation differences | 4,198 | (2,140) | 4,818 |
| Balance at 31 December | 150,432 | 123,656 | 84,740 |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Short term contract assets relate to contractual obligations from contract fractionation agreements entered into by Biotest AG. The resulting performance obligations are generally fulfilled by Biotest over a period of up to 12 months. Receivables from this business, which usually have a due date of between 90 and 120 days, are recognized when the right to receive the consideration becomes unconditional. This is the case when the biological drugs produced from the blood plasma provided by the customer are delivered to the customer. These are service transactions that are valued at the corresponding costs of sales incurred plus profit margin, if it can be estimated.
Details of short term contract assets at 31 December 2024 and 2023 are as follows:
| Thousands of Euros | ||
|---|---|---|
| 31/12/2024 | 31/12/2023 | |
| Contract assets (gross) | 36,074 | 47,839 |
| Allowances for expected credit losses | (96) | (88) |
| Contract assets (net) | 35,978 | 47,751 |
Default risks are accounted for by making value adjustments to the contract assets. The allowance for expected credit losses is calculated as the difference between the nominal amount of the contract assets and the estimated recoverable amount.
Movement in allowance for expected credit losses corresponding to contract assets is included in note 30.
Details at 31 December 2024 and 2023 are as follows:
| Thousands of Euros | ||||
|---|---|---|---|---|
| Reference | 31/12/2024 | 31/12/2023 | ||
| Trade receivables | 677,147 | 449,139 | ||
| Receivables from associates | Note 31 | 38,657 | 227,550 | |
| Impairment losses | Note 30 (i) | (10,352) | (31,576) | |
| Trade receivables | 705,452 | 645,113 | ||
| Other receivables | Note 30 (i) | 10,529 | 27,444 | |
| Personnel | 1,489 | 1,123 | ||
| Advance payments | Note 30 (i) | 5,590 | 4,150 | |
| Taxation authorities, VAT recoverable | 53,532 | 32,587 | ||
| Other public entities | 6,416 | 9,629 | ||
| Other receivables | 77,556 | 74,933 | ||
| Current income tax assets | 52,589 | 47,213 | ||
| Total trade and other receivables | 835,597 | 767,259 |
During 2024, 2023 and 2022, the Grifols Group has sold receivables without recourse to some financial institutions (factors), to which the risks and benefits inherent to the ownership of the assigned credits are substantially transferred. Also, the control over the assigned credits, understood as the factor's ability to sell them to an unrelated third party, unilaterally and without restrictions, has been transferred to the factor.
The main conditions of these contracts include the advanced collection of the assigned credits that vary between 70% and 100% of the nominal amount and a percentage of insolvency risk coverage on the factor side that varies between 90% and 100% of the nominal of the assigned credits.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
These contracts have been considered as without recourse factoring and the amount advanced by the factors has been derecognized from the balance sheet.
Likewise, in financial years 2024, 2023 and 2022, some receivables assignment contracts were signed with a financial institution, in which the Group retains the risks and benefits inherent to the ownership of the assigned credits. These contracts have been considered as factoring with recource and the assigned amount remains in the consolidated balance sheet at year end and a short-term debt is recognized for an amount equal to the consideration received from the factor for the assignment. There is no amount recognized at 31 December 2024 (Euros 16,985 thousand at 31 December 2023).
At 31 December 2024, the finance cost of credit rights sold for the Group totals Euros 30,782 thousand which has been recognized under finance costs in the consolidated statement of profit and loss for (Euros 24,993 thousand in 2023 and Euros 18,201 thousand in 2022) (note 27).
The volume of invoices sold without recourse to various financial institutions which, based on their due date would not have been collected at 31 December 2024, totals Euros 334,430 thousand (Euros 391,886 thousand at 31 December 2023).
Details of balances with related parties are shown in note 31.
Details of this caption of the consolidated balance sheet at 31 December 2024 and 2023 are as follows:
| Thousands of Euros | ||
|---|---|---|
| 31/12/2024 | 31/12/2023 | |
| Current deposits | 5,100 | 6,506 |
| Cash in hand and at banks | 974,680 | 523,071 |
| Total cash and cash equivalents | 979,780 | 529,577 |
Details of consolidated equity and movement are shown in the consolidated statement of changes in equity.
At 31 December 2024 and 2023, the Company's share capital amounts to Euros 119,603,705 and comprises:
Our Class B shares have substantially similar dividend and other economic rights as our Class A shares, but differ from the Class A shares in some important respects that are outlined below.
Holders of our Class B shares generally do not have voting rights, except with respect to certain extraordinary matters, with respect to which approval by a majority of our outstanding Class B shares is required.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Notwithstanding the lack of voting rights of our Class B shares generally, resolutions on the matters detailed below (each, an"extraordinary matter") require the approval of a majority of our outstanding Class B shares.
The general shareholders' meeting has the power to decide on all matters assigned to it by law or by the Articles of Association and, in particular, without limitation to the foregoing, shall be the only corporate body or office entitled to decide on these extraordinary matters.
Each of our Class B shares entitles its holder to receive a minimum annual preferred dividend out of the distributable profits at the end of each fiscal year the share is outstanding equal to Euros 0.01 per Class B share. In any given fiscal year, we will pay a preferred dividend to the holders of our Class B shares before any dividend out of the distributable profits for such fiscal year is paid to the holders of our Class A shares. The preferred dividend on all issued Class B shares will be paid by us within the nine months following the end of that fiscal year, in an amount not to exceed the distributable profits obtained by us during that fiscal year.
If, during a fiscal year, we have not obtained sufficient distributable profits to pay in full, out of those profits, the preferred dividend on all the Class B shares outstanding, the preferred dividend amount exceeding the distributable profits obtained by us will not be paid and will not be accumulated as a dividend payable in the future.
Lack of payment, total or partial, of the preferred dividend during a fiscal year due to insufficient distributable profits to pay in full the preferred dividend for that fiscal year will not cause our Class B shares to recover any voting rights.
Each Class B share is entitled to receive, in addition to the preferred dividend referred to above, the same dividends and other distributions (in each case, whether in cash, securities of Grifols or any of our subsidiaries, or any other securities, assets or rights) as one Class A share. Each Class B share is treated as one Class A share for the purpose of any dividends or other distributions made on our Class A shares, including as to the timing of the declaration and payment of any such dividend or distribution.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Each holder of our Class B shares is entitled to redeem those shares as set forth in this section if a tender offer for all or part of our share capital is made and settled (in whole or in part), except if holders of our Class B shares were entitled to (i) participate in such offer and (ii) have their shares acquired in such offer equally and on the same terms as holders of our Class A shares (including, without limitation, for the same consideration).
Upon the closing and settlement (in whole or in part) of a tender offer for our shares in which holders of our Class B shares were not entitled to (i) participate and (ii) have their shares acquired in such offer equally and on the same terms as holders of our Class A shares (including, without limitation, for the same consideration), the redemption process will follow the process detailed below.
The number of our Class B shares redeemed shall not represent a percentage over our total Class B shares issued and outstanding at the time the tender offer is made in excess of the percentage that the sum of our Class A shares (i) to which the tender offer is addressed, (ii) held by the offerors in that offer and (iii) held by persons acting in concert with the offerors or by persons having reached an agreement relating to the offer with the offerors represent over the total Class A shares issued and outstanding at the time the tender offer causing the redemption of our Class B shares is made.
Payment of the redemption price will be subject to us having sufficient distributable reserves but, after a tender offer occurs and until the redemption price for our Class B shares is paid in full, we will not be able to declare or pay any dividends nor any other distributions to our shareholders (in each case, whether in cash, securities of Grifols or any of our subsidiaries, or any other securities,assets or rights).
Each Class B share entitles its holder to receive, upon our winding-up and liquidation, an amount equal to the sum of (i) the nominal value of such Class B share and (ii) the share premium paid up for such Class B share when it was subscribed for.
We will pay the liquidation amount to the holders of our Class B shares before any amount on account of liquidation is paid to the holders of our Class A shares.
Each of our Class B shares entitles its holder to receive, in addition to the liquidation preference amount, the same liquidation amount paid for a Class A share.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Each Class B share entitles its holder to the same rights (including preferential subscription rights and free allotment rights) as one Class A share in connection with any issuance, granting or sale of (i) any shares in Grifols, (ii) any rights or other securities exercisable for, exchangeable or convertible into shares in Grifols or (iii) any options, warrants or other instruments giving the right to the holder thereof to purchase, convert, subscribe or otherwise receive any securities in Grifols.
As an exception, the preferential subscription rights and the free allotment rights of the Class B shares will only be for new Class B shares or for instruments giving the right to purchase, convert, subscribe for or otherwise receive Class B shares, and the preferential subscription right and the free allotment right of an Class A share will only be for new Class A shares or for instruments giving the right to purchase, convert, subscribe or otherwise receive Class A shares, for each capital increase or issuance that meets the following three requirements: (i) the issuance of Class A shares and Class B shares is in the same proportion of our share capital as they represent at the time the resolution on the capital increase is passed; (ii) grants of preferential subscription rights or free allotment rights,as applicable, to the Class B shares for the Class B shares are under the same terms as the preferential subscription rights or free allotment rights, as applicable, granted to the Class A shares for the Class A shares; and (iii) no other shares or securities are issued.
Class B shares are in book-entry form on Iberclear and are indivisible, in the same terms as the Class A shares.
Since 23 July 2012 the ADSs (American Depositary Shares) representing Grifols' Class B shares (non-voting shares) have had an exchange ratio of 1:1 in relation to Class B shares, ie.1 ADS represents 1 Class B share. The previous rate was 2 ADS per 1 Class B share.
The Company's knowledge of its shareholders is based on information provided voluntarily or in compliance with applicable legislation. According to the information available to the Company, there are no interests representing more than 10% of the Company's total capital at 31 December 2024 and 2023 (note 17(g)).
At 31 December 2024 and 2023, the number of outstanding shares is equal to the total number of Company shares, less treasury stock.
Movement in outstanding shares during 2024 is as follows:
| Reference | Class A shares | Class B shares | |
|---|---|---|---|
| Balance at 1 January 2024 | 422,185,368 | 256,906,911 | |
| (Acquisition) / disposal of treasury stock | Note 17(d) | — | 1,316,825 |
| Balance at 31 December 2024 | 422,185,368 | 258,223,736 |
Movement in outstanding shares during 2023 is as follows:
| Reference | Class A shares | Class B shares | |
|---|---|---|---|
| Balance at 1 January 2023 | 422,185,368 | 256,225,326 | |
| (Acquisition) / disposal of treasury stock | Note 17(d) | — | 681,585 |
| Balance at 31 December 2023 | 422,185,368 | 256,906,911 |
Movement in the share premium is described in the consolidated statement of changes in equity, which forms an integral part of this note to the consolidated annual accounts.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The drawdown of accumulated gains is subject to legislation applicable to each of the Group companies.
The movement in this caption of the consolidated balance sheet during the years ended at 31 December 2024, 2023 and 2022 is reflected in the consolidated statement of changes in equity. The most significant movements in the current year relate to the acquisitions of Haema Plasma Kft, Grifols Pyrenees Research Center, S.L., and Grifols Malaysia SDN BHD (note 2). The first two acquisitions had a negative impact on reserves, decreasing them by Euro 14,022 thousand and Euro 356 thousand, respectively. On the other hand, the acquisition of Grifols Malaysia SDN BHD generated a positive effect, increasing reserves by Euros 4,679 thousand.
Companies in Spain are obliged to transfer 10% of each year's profits to a legal reserve until this reserve reaches an amount equal to 20% of share capital. This reserve is not distributable to shareholders and may only be used to offset losses if no other reserves are available. Under certain conditions it may be used to increase share capital provided that the balance left on the reserve is at least equal to 10% of the nominal value of the total share capital after the increase.
At 31 December 2024 and 2023 the legal reserve of the Parent amounts to Euros 23,921 thousand which corresponds to 20% of the share capital.
Distribution of the legal reserves of Spanish companies is subject to the same restrictions as those of the Company and at 31 December 2024 the balance of the legal reserve of other Spanish companies amounts to Euros 2,171 thousand (Euros 1,711 thousand at 31 December 2023).
Other foreign Group companies have a legal reserve amounting to Euros 3,744 thousand at 31 de diciembre de 2024 (Euros 4,227 thousand at 31 December 2023).
At 31 December 2024, Euros 18,925 thousand equivalent to the carrying amount of development costs pending amortization of certain Spanish companies (Euros 7,179 thousand at 31 December 2023) are, in accordance with applicable legislation, a distribution limitation until these development costs have been amortized.
The hedging reserve includes the cash flow hedge reserve and the costs of hedging reserve, see note 4(i) or details. The cash flow hedge reserve is used to recognize the effective portion of gains or losses on derivatives that are designated and qualify as cash flow hedges, as described in note 30.
The Group defers the changes in the forward element of forward contracts and the time value of option contracts in the costs of hedging reserve.
The Parent held Class A and B treasury stock equivalent to 1,0% of its capital at 31 December 2024 (1.2% of its capital in Class A and B treasury stock at 31 December 2023).
During the years ended at 31 December 2024 and 2023 there have been no movements in Class A treasury shares, with a total of 3,944,430 shares and 89,959 thousand euros.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Movement in Class B treasury stock during 2024 is as follows:
| No. of Class B shares | Thousands of Euros | |
|---|---|---|
| Balance at 1 January 2024 | 4,518,199 | 62,789 |
| Disposal Class B shares | (1,316,825) | (18,300) |
| Balance at 31 December 2024 | 3,201,374 | 44,489 |
In April and October 2024, the Group delivered 1,316,825 treasury stocks (Class B shares) to eligible employees as compensation under the Restricted Share Unit Retention Plan.
Movement in Class B treasury stock during 2023 was as follows:
| No. of Class B shares | Thousands of Euros | |
|---|---|---|
| Balance at 1 January 2023 | 5,199,784 | 72,261 |
| Disposal Class B shares | (681,585) | (9,472) |
| Balance at 31 December 2023 | 4,518,199 | 62,789 |
In March, May and October 2023, the Group delivered 681,585 treasury stocks (Class B shares) to eligible employees as compensation under the Restricted Share Unit Retention Plan.
The profits of Grifols, S.A. and subsidiaries will be distributed as agreed by respective shareholders at their general meetings.
The proposed distribution of profit of the Parent Grifols, S.A. for the years ended 31 December 2024,and the distribution of profit approved for 2023, presented at the general meeting held on 14 June 2024, is as follows:
| Thousands of Euros | |||
|---|---|---|---|
| 31/12/2024 | 31/12/2023 | ||
| Voluntary reserve | (83,138) (246,735) |
||
| Losses of the Parent | (83,138) (246,735) |
The distribution of profit corresponding to the year ended 31 December 2024 and 2023 presented in the statement of changes in consolidated equity.
At 31 December 2024 and 2023, no dividend or interim dividend have been paid
The Group has set up a Restricted Share Unit Retention Plan (hereinafter RSU Plan) and a long-term incentive plan for certain employees (note 29).This commitment will be settled using equity instruments and the cumulative accrual amounts to Euros 6,648 thousand at 31 December 2024 (Euros 8,282 thousand at 2023).
The incentive plan that has been granted equity instruments to certain employees as part of their compensation package, subject to the achievement of various metrics, both financial and non-financial. The plan has been assessed by calculating the unit value of the options at the valuation date and multiplying it by the total number of options to be granted. Subsequently, this unit value will be adjusted based on the likelihood of achieving the specified objectives.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The most significant shareholdings in the share capital of Grifols, S.A. as of December 31, 2024, according to publicly available information or communication made to the Company, are as follows:
| % of voting rights attached to the shares |
% of voting rights through financial instruments |
% of total voting |
|||
|---|---|---|---|---|---|
| Name or company name of shareholder | Direct | Indirect | Direct | Indirect | rights |
| Marc P. Andersen | — % | 3.13 % | — % | — % | 3.13 % |
| BlackRock, Inc. | — % | 2.90 % | — % | 1.41 % | 4.31 % |
| Capital Research and Management Company | — % | 3.68 % | — % | 0.90 % | 4.58 % |
| Deria, S.A. | 9.20 % | — % | — % | — % | 9.20 % |
| Europacific Growth Fund | 2.88 % | — % | 0.35 % | — % | 3.23 % |
| Flat Footed Llc. | — % | 3.13 % | — % | — % | 3.13 % |
| JPMorgan Chase & Co. | — % | — % | — % | 3.32 % | 3.32 % |
| Mason Capital Master Fund L.P. | — % | 2.11 % | — % | — % | 2.11 % |
| Melqart Opportunities Master Fund Ltd. | — % | — % | 1.06 % | — % | 1.06 % |
| Ponder Trade, S.L. | 7.09 % | — % | — % | — % | 7.09 % |
| Ralledor Holding Spain, S.L. | 6.15 % | — % | — % | — % | 6.15 % |
| Rokos Global Macro Master Fund Lp. | — % | — % | 1.14 % | — % | 1.14 % |
| Scranton Enterprises, B.V. | 8.40 % | — % | — % | — % | 8.40 % |
| Armistice Capital Master Fund Ltd | 1.06 % | — % | — % | — % | 1.06 % |
The calculation of basic earnings per share is based on the profit for the year attributable to the shareholders of the Parent divided by the weighted average number of ordinary shares outstanding throughout the year, excluding treasury stock.
Details of the calculation of basic earnings per share are as follows:
| 31/12/2024 | 31/12/2023 (*) | 31/12/2022(*) | |
|---|---|---|---|
| Profit for the year attributable to shareholders of the Parent (Thousands of Euros) |
156,920 | 42,318 | 185,035 |
| Weighted average number of ordinary shares outstanding | 679,668,551 | 679,756,294 | 679,805,142 |
| Basic earnings per share (Euros per share) | 0.23 | 0.06 | 0.27 |
(*) Restated figures (Note 2.d)
The basic earnings per share (Euros per share) for the years 2023 and 2022 before the restatement detailed in note 2(d)were Euros 0.09 and Euros 0.31 respectively.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The weighted average number of ordinary shares outstanding (basic) is as follows:
| Number of shares | ||||
|---|---|---|---|---|
| 31/12/2024 | 31/12/2023 | 31/12/2022 | ||
| Issued shares outstanding at 1 January Effect of treasury stock |
679,092,279 576,272 |
679,469,076 287,218 |
679,598,330 206,812 |
|
| Weighted average number of ordinary shares outstanding (basic) at 31 December |
679,668,551 | 679,756,294 | 679,805,142 |
Diluted earnings per share are calculated by dividing profit for the year attributable to shareholders of the Parent by the weighted average number of ordinary shares outstanding considering the diluting effects of potential ordinary shares.
The RSUs granted by the Group and payable in shares, assumes the existence of dilutive potential shares. Diluted earnings per share have been calculated as follows:
| 31/12/2024 | 31/12/2023(*) | 31/12/2022(*) | |
|---|---|---|---|
| Profit for the year attributable to shareholders of the Parent (Thousands of Euros) |
156,920 | 42,318 | 185,035 |
| Weighted average number of ordinary shares outstanding (diluted) | 679,916,715 | 677,101,992 | 679,292,729 |
| Diluted earnings per share (Euros per share) | 0.23 | 0.06 | 0.27 |
(*) Restated figures (Note 2.d)
The diluted earnings per share (Euros per share) for the years 2023 and 2022 before the restatement detailed in note 2(d) were Euros 0.09 and Euros 0.31 respectively.
The weighted average number of ordinary shares outstanding diluted has been calculated as follows:
| Number of shares | ||||
|---|---|---|---|---|
| 31/12/2024 31/12/2023 |
31/12/2022 | |||
| Ordinary shares outstanding at 1 January | 679,092,279 | 679,469,076 | 679,598,330 | |
| Plans of rights over shares | 248,164 | (2,654,302) | (512,413) | |
| Effect of treasury stock | 576,272 | 287,218 | 206,812 | |
| Weighted average number of ordinary shares outstanding (diluted) at 31 December |
679,916,715 | 677,101,992 | 679,292,729 |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Details of non-controlling interests and movement at 31 December 2024 are as follows:
| Thousands of Euros | ||||||||
|---|---|---|---|---|---|---|---|---|
| Referenc e |
Balance at 31/12/2023 |
Additions | Business combinations / Perimeter additions |
Dividends | Other movements |
Translation differences |
Balance at 31/12/2024 |
|
| Grifols (Thailand) Pte Ltd | 5,244 | 213 | — | (65) | — | 345 | 5,737 | |
| Grifols Malaysia Sdn Bhd | 4,230 | 180 | (4,697) | — | — | 287 | — | |
| Araclon Biotech, S.A. | (1,137) | (267) | — | — | — | — | (1,404) | |
| Haema GmbH | 253,620 | 6,191 | — | — | — | — | 259,811 | |
| BPC Plasma, Inc | 147,657 | 27,722 | — | (39,509) | 14 | 9,718 | 145,602 | |
| Grifols Diagnostics Solutions Inc. | 1,347,323 | 47,619 | 507,803 | (25,400) | 396 | 92,365 | 1,970,106 | |
| Plasmavita Healthcare | 12,768 | 3,693 | — | — | — | — | 16,461 | |
| Haema Plasma Kft | Note 2 (b) | 20,344 | 204 | (20,978) | — | — | 430 | — |
| G Pyrenees Research Cntr | 22 | (179) | 157 | — | — | — | — | |
| Albimmune SL | (1,762) | (805) | — | — | — | — | (2,567) | |
| Biotest AG | 357,010 | (28,685) | — | (898) | — | 2,125 | 329,552 | |
| 2,145,319 | 55,886 | 482,285 | (65,872) | 410 | 105,270 | 2,723,298 |
On October 22, 2024, the Group acquired the entirety of Haema Plasma Kft., as detailed in note 2(b), which has resulted in a reduction of said non-controlling interest in its entirety.
Additionally, in the context of the agreement for the sale of the 20% stake in SRAAS (note 12), the effective percentage of the non-controlling interest in Grifols Diagnostic Solutions Inc. has increased by 11.96% reaching a 45%, representing an increase in the equity attributed to minority parties of Euros 507,803 thousand .
In 2024, Grifols Diagnostic Solutions Inc. has distributed a dividend of US Dollar 60 million, having an impact against Group's non-controlling reserves of Euros 25,400 thousand. Furthermore, BPC Plasma, Inc. has made a distribution of dividends without cash outflow and in compensation for "Other loans to related parties" to its shareholder Scranton Plasma B.V. worth Euros 39,509 thousand (notes 11 and 31).
Details of non-controlling interests and movement at 31 December 2023 are as follows:
| Thousands of Euros | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Reference Balance at 31/12/2022 |
Additions | Business combinations / Perimeter additions |
Dividends | Other movements |
Translation differences |
Balance at 31/12/2023 |
|||
| Grifols (Thailand) Pte Ltd | 4,779 | 642 | — | (28) | — | (149) | 5,244 | ||
| Grifols Malaysia Sdn Bhd | 3,663 | 850 | — | — | — | (283) | 4,230 | ||
| Araclon Biotech, S.A. | (593) | (544) | — | — | — | — | (1,137) | ||
| Kiro Grifols, S.L. | (25) | (301) | 326 | — | — | — | — | ||
| Haema GmbH | 228,684 | 24,936 | — | — | — | — | 253,620 | ||
| BPC Plasma, Inc | 354,502 | 67,892 | — | (266,406) | 11 | (8,342) | 147,657 | ||
| Grifols Diagnostics Solutions Inc. | 1,353,674 | 39,670 | — | — | 74 | (46,095) | 1,347,323 | ||
| Plasmavita Healthcare | 10,134 | 2,634 | — | — | — | — | 12,768 | ||
| Haema Plasma Kft | Nota 2 (b) | 11,939 | 7,769 | — | — | — | 636 | 20,344 | |
| G Pyrenees Research Cntr | (6) | (12) | — | — | 40 | — | 22 | ||
| Albimmune SL | (741) | (1,021) | — | — | — | — | (1,762) | ||
| Biotest AG | 361,596 | (21,161) | 6,283 | — | (64) | 10,356 | 357,010 | ||
| 2,327,606 | 121,354 | 6,609 | (266,434) | 61 | (43,877) | 2,145,319 |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
During the 2023 financial year, BPC Plasma, Inc. distributed a dividend without cash outflow compensating "Other loans to related parties". This dividend corresponded to the result of the previous 4 financial years, valued at Euros 266,406 thousand to its shareholder Scranton Plasma B.V. This distribution had an impact against the Group's noncontrolling interests reserves (note 11).
During 2023, Grifols' stake in SRAAS increased from 26.20% to 26.58% as a result of the purchase of SRAAS's own shares. Therefore, the effective percentage of non-controlling interest was reduced from 33.21% to 33.04%.
At 31 December 2024 and 2023, the main items of the statement of financial positions of the most significant noncontrolling interests are as follows:
| Thousands of Euros | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| 31/12/2024 | ||||||||||
| Non current assets |
Current assets |
Non current liabilities |
Current liabilities |
Equity | Consolidated Adjustments |
Total Consolidated Equity |
% Non controlling Interest |
Non controlling interests |
||
| Grupo Biotest | 617,792 | 808,684 | (743,237) | (159,120) | 524,119 | 581,020 | 1,105,139 | 29.8 % | 329,552 | |
| Grupo GDS | 4,626,938 | 253,256 | (367,987) | (134,193) | 4,378,014 | — | 4,378,014 | 45.0 % | 1,970,106 | |
| Haema GmbH | 58,753 | 120,902 | (33,986) | (50,293) | 95,376 | 164,435 | 259,811 | 100.0 % | 259,811 | |
| BPC Plasma, Inc | 86,112 | 26,085 | (53,382) | (22,236) | 36,579 | 109,023 | 145,602 | 100.0 % | 145,602 | |
| 5,389,595 | 1,208,927 | (1,198,592) | (365,842) | 5,034,088 | 854,478 | 5,888,566 | 2,705,071 |
| Thousands of Euros | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| 31/12/2023 | |||||||||
| Non current assets |
Current assets |
Non current liabilities |
Current liabilities |
Equity | Consolidated Adjustments |
Total Consolidated Equity |
% Non controlling Interest |
Non controlling interests |
|
| Grupo Biotest | 654,481 | 756,382 | (528,649) | (383,361) | 498,853 | 698,365 | 1,197,218 | 29.8 % | 357,010 |
| Grupo GDS | 4,216,198 | 273,576 | (323,673) | (109,121) | 4,056,980 | — | 4,056,980 | 33.2 % | 1,347,323 |
| Haema GmbH | 61,271 | 127,818 | (28,859) | (74,680) | 85,550 | 168,070 | 253,620 | 100.0 % | 253,620 |
| BPC Plasma, Inc | 84,037 | 23,043 | (48,510) | (19,329) | 39,241 | 108,416 | 147,657 | 100.0 % | 147,657 |
| 5,015,987 | 1,180,819 | (929,691) | (586,491) | 4,680,624 | 974,851 | 5,655,475 | 2,105,610 |
| Thousands of Euros | Thousands of Euros 2023 |
||||||||
|---|---|---|---|---|---|---|---|---|---|
| 2024 | |||||||||
| Ordinary Income |
Consolidated Net Income |
% Non controlling Interest |
Non controlling interests |
Ordinary Income |
Consolidated Net Income |
% Non controlling Interest |
Non controlling interests |
||
| Biotest group | 726,317 | (96,194) | 29.8 % | (28,685) | 684,521 | (70,962) | 29.8 % | (21,161) | |
| GDS Group | 578,000 | 122,440 | 45.0 % | 47,619 | 605,851 | 119,453 | 33.2 % | 39,670 | |
| Haema GmbH | 203,664 | 6,191 | 100.0 % | 6,191 | 194,892 | 24,936 | 100.0 % | 24,936 | |
| BPC Plasma, Inc | 223,755 | 27,720 | 100.0 % | 27,722 | 248,918 | 67,892 | 100.0 % | 67,892 | |
| 1,731,736 | 60,157 | 52,847 | 1,734,182 | 141,319 | 111,337 |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Detail of cash flows of the most significant non-controlling interests is as follows:
| Thousands of Euros | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | ||||||||
| Haema GmbH |
BPC Plasma |
Biotest Group |
GDS Group |
Haema GmbH |
BPC Plasma |
Biotest Group |
GDS Group |
||
| Net cash flows from operating activities | 17,640 | 39,188 | 62,960 | 212,945 | 23,278 | 5,814 | (3,608) | 232,418 | |
| Net cash flows from investing activities | (11,474) | (32,996) | (26,702) | (53,711) | (28,367) | (8,421) | 209 | (204,591) | |
| Net cash flows from financing activities | — | — | (36,427) | (159,695) | — | — | (4,829) | (27,378) | |
| 6,166 | 6,192 | (169) | (461) | (5,089) | (2,607) | (8,228) | 449 |
In mid-2018, Grifols acquired 100% of the shares of Haema GmbH and BPC Plasma, Inc., which were subsequently sold to Scranton in December 2018, for the same amount and conditions under which they were acquired.
The following indicators support the power that Grifols maintains over these companies, even after their sale to Scranton and that, therefore, it retains control over Haema and BPC in accordance with IFRS 10:
As a result of all of the above, Grifols has the power to direct the relevant activities of these companies, since it manages them and jointly determines their business plan, having the unilateral right to repurchase 100% of both companies. The fact that Grifols has a currently exercisable purchase option implies that it acts as principal in the exercise of power (i) through the management contract and (ii) by not having delegated said power. Therefore, Grifols maintains control in both companies and therefore consolidates them.
In relation to the purchase option and given that it is based on a variable number of shares and a variable acquisition price, said instrument is a derivative financial instrument that must be valued at fair value with changes in the profit and loss account.
Based on the abovementioned contractual conditions, Grifols has estimated the value of the exercise of the repurchase option as follows: (i) the price at which the Selling Companies sold the shares to Scranton (totalling USD 538,000,000) increased by any expenses relating to the completion of the transactions contemplated in the relevant share purchase agreement, plus (ii) the change in working capital. Based on the business models of Haema and BPC, this change in working capital is expected to primarily reflect the undistributed profits at the time of exercise of the
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
repurchase option. Given that the price of the exercise of the repurchase option aligns closely with the fair value of BPC and Haema, this option's overall value is not considered significant. Furthermore, since the valuation of the option relies on unobservable market factors, it falls under Level 3 of the fair value hierarchy. Considering the uncertainties underlying the valuation of the option as it deals with non-observable variables, and the value of the same not being significant, said value has not been recognized as a 31 December 2024 and 2023 (not 29).
Previous to the sale of the 20% participation in SRAAS, there was an indirect participation:
Since IAS 28 does not address how to account for cross-participations, Grifols opted to: in the equity method of integration of the result of SRAAS, the result that SRAAS recognized when integrating the result of GDS by its percentage of participation (45% of GDS) was excluded. Therefore, Grifols' consolidated result did not include 11.96% of GDS's result recognized in SRAAS (equivalent to 45%*26.58%) to avoid duplications, since the GDS Group is consolidated by global integration.
When determining the allocation of the GDS result attributed to the non-controlling interest (SRAAS), SRAAS's percentage of participation in GDS was adjusted by 11.96% and therefore, the percentage to attribute the result was 33.04% (45% - 11.96%) and 33.21% for the period ended as of 31 December 2023 and 31 December 2022 respectively.
As a result of the sale transaction (note 12), Grifols now owns 6,58% of the participation in SRAAS (financial investment), so it losses its significant influence over its interest in SRAAS and, consequently, its indirect 11.96% stake in GDS' capital that it held. In the current year, the effective percentage of non-controlling interest recognized in GDS increased to 45%.
Grifols, S.A. has control over Grifols Diagnostic Solutions, Inc (hereinafter GDS) through Grifols Shared Services North America, Inc (hereinafter GSSNA), following the entry of the new shareholder Shanghais RAAS Blood Products Co Ltd (hereinafter SRAAS).
Grifols, S.A., through GSSNA, owns 60% of the Class A shares with voting rights and 50% of the Class B shares without voting rights, with both classes of shares having the same economic rights, so the economic rights amount to 55%. SRAAS owns 40% of class A shares and 50% of class B shares and economic rights of 45%.
Both shareholders have the right of first refusal in the event of a sale of the stake by each of the parties. In addition, SRAAS has certain veto rights, although Grifols has control over GDS for the following reasons:
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Details of provisions at 31 December 2024 and 2023 are as follows:
| Thousands of Euros | ||||
|---|---|---|---|---|
| 31/12/2024 | 31/12/2023 | |||
| Provisions for pensions and similar obligations (a) | 102,126 | 100,159 | ||
| Other provisions | 22,922 | 16,766 | ||
| Non-current provisions | 125,048 | 116,925 | ||
| Trade provisions | 25,089 | 39,695 | ||
| Other provisions | 13,524 | 8,111 | ||
| Current provisions | 38,613 | 47,806 |
The movement in non-current and current provisions is as follows:
| Reference | 31/12/2024 | 31/12/2023 | 31/12/2022 | |
|---|---|---|---|---|
| Opening balance | 164,731 | 166,402 | 55,529 | |
| Business combinations | Note 3 | — | — | 138,476 |
| Net charges | 9,261 | 28,696 | 12,588 | |
| Net cancellations | (15,019) | (19,571) | (9,091) | |
| Transfers | 3,526 | (9,550) | (33,575) | |
| Translation differences | 1,162 | (1,246) | 2,475 | |
| Closing balance | 163,661 | 164,731 | 166,402 |
At 31 December 2024, 2023 and 2022, the balance of provisions for pensions and similar mainly includes provisions made by the Biotest Group in relation to retirement benefit obligations and employment commitments with certain employees.
Benefits are based on the employee's length of service and salary. Retirement benefit obligations relate mainly to employees of the Group's German companies. Similar obligations are foreign obligations payable in a lump sum on retirement and obligations of the pension savings plan. These plans are voluntary pension plans not subject to statutory or legal obligations. The amount of the pension obligations is mainly dependent on interest rate movements and the life expectancy of the participants.
In financial year 2024, assets of Euros 11,162 thousand , were mainly held by a trustee, company of the group, under a contractual trust arrangement (CTA) as external insolvency insurance for portions of the occupational pension scheme (Euros 10,757 thousand at 31 December 2023). Since the transferred funds qualify as plan assets in accordance with IAS 19, provisions for pensions and similar obligations were netted with the transferred assets. As a result, provisions for pensions and similar obligations were reduced accordingly.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
At 31 December 2024 and 2023, the net defined benefit liability of the Group comprises the following:
| Thousands of Euros | ||
|---|---|---|
| 31/12/2024 | 31/12/2023 | |
| From pension plans | 95,555 | 95,721 |
| From similar obligations | 17,733 | 15,195 |
| Net present value of defined benefit obligations | 113,288 | 110,916 |
| For pension plans | 9,011 | 8,738 |
| For similar obligations | 2,151 | 2,019 |
| Fair value of plan assets | 11,162 | 10,757 |
| From pension plans | 86,544 | 86,983 |
| From similar obligations | 15,582 | 13,176 |
| Net defined benefit liability | 102,126 | 100,159 |
The costs for the defined benefit plans consist of the following components:
| Thousands of Euros | ||
|---|---|---|
| 31/12/2024 | 31/12/2023 | |
| Current service cost | 4,704 | 5,204 |
| Net interest expenses | 3,361 | 3,536 |
| Total expenses recognised in profit and loss | 8,065 | 8,740 |
| Actuarial (gains)/losses due to experience adjustments | (1,914) | (1,131) |
| Actuarial (gains)/losses due to changes in financial assumptions | (1,206) | 4,200 |
| Return on plan assets (excluding amounts included in net interest expense) | (111) | (227) |
| Revaluation recognised directly in other comprehensive income | (3,231) | 2,842 |
| Defined benefit costs | 4,834 | 11,582 |
In financial year 2024, actuarial gains of Euros 3,120 thousand are recognized in other comprehensive income (actuarial losses of Euros 3,069 thousand at 31 December 2023). Of this amount, a gain of Euros 1,206 thousand resulted from changes in actuarial assumptions (Euros 4,200 thousand of losses at 31 December 2023),which is mainly due to the increase in the actuarial interest rate in the main plans in Germany from 3.5% to 3.4% (increase in the actuarial interest rate in the main plans in Germany from 3.9% to 3.4% in 2023).
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The following table shows the reconciliation of the net present value of the defined benefit obligation (DBO):
| Thousands of Euros | ||
|---|---|---|
| 31/12/2024 | 31/12/2023 | |
| Net present value of defined benefit obligation | 110,916 | 102,693 |
| Current service cost | 5,656 | 5,136 |
| Interest expense | 3,361 | 3,536 |
| Expenses recognised in the statement of profit and loss | 9,017 | 8,672 |
| Actuarial losses due to experience adjustments | (1,914) | (1,131) |
| Actuarial gains due to changes in financial assumptions | (1,206) | 4,200 |
| Revaluation recognised directly in other comprehensive income | (3,120) | 3,069 |
| Pension benefits paid | (3,525) | (3,518) |
| Net present value of defined benefit obligations at 31 December | 113,288 | 110,916 |
The following table shows the reconciliation of the fair value of plan assets:
| Thousands of Euros | ||
|---|---|---|
| 31/12/2024 | 31/12/2023 | |
| Fair value of plan assets | 10,756 | 8,622 |
| Interest income | 268 | 95 |
| Income recognised in the consolidated statement of income | 268 | 95 |
| Return on plan assets (excluding amounts included in net interest expenses) | (145) | (108) |
| Revaluations recognised directly in the statement of comprehensive income | (145) | (108) |
| Contribution by the employer | 307 | 2,208 |
| Payments from plan assets | (24) | (60) |
| Fair value of plan assets as of 31 December | 11,162 | 10,757 |
The following payments are expected to be made in subsequent years based on the current pension obligations of the Group:
| Thousands of Euros | ||
|---|---|---|
| 31/12/2024 | 31/12/2023 | |
| In the next 12 months | 6,550 | 5,239 |
| Between 2 and 5 years | 22,756 | 22,369 |
| Between 5 and 10 years | 30,402 | 31,307 |
| After 10 years | 127,256 | 122,746 |
| Total expected payments | 186,964 | 181,661 |
The weighted average term of the defined benefit plans is 11.7 years as of 31 December 2024 (11.6 years at 31 December 2023).
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Plan assets of the Group were invested in the following asset classes as of the reporting date:
| Thousands of Euros | ||
|---|---|---|
| 31/12/2024 | 31/12/2023 | |
| Cash and cash equivalents | 2,941 | 102 |
| Financial investment | 131 | 2,750 |
| Fund shares | 8,090 | 7,905 |
| Total assets | 11,162 | 10,757 |
The plan assets transferred are invested in accordance with defined investment principles, whereby the maturity or termination option of the financial instruments must always be selected in such a way that the association can meet its payment obligations. In accordance with the investment principles, the assets can be invested in Euro time deposits as well as domestic government bonds, mortgage bonds or fund units in money market funds or corporate bonds, all in Euro. Loans can also be issued to the Group companies against the corresponding guarantees. A minimum rating of A- is required for all financial instruments.
The calculation of the pension plans is based on the following actuarial assumptions:
| 31/12/2024 | 31/12/2023 | |
|---|---|---|
| Discount rate | 3.5% | 3.4% |
| Expected return on plan assets | 3.4% | 1.7% |
| Rate of increase for wages and salaries | 3.4% | 3.4% |
| Rate of interest for pensions | 2.0% | 2.0% |
| Employee turnover rate | 3.0% | 3.0% |
Actuarial assumptions are mainly based on historical empirical values with the exception of the discount rate. The calculation was based on the published Heubeck 2018 G mortality tables.
Under IAS 19.145, the effect of any possible changes to parameters for the underlying assumptions used to calculate the pension obligations must be disclosed in the sensitivity analysis. Only changes that are realistically expected to occur in the following financial year are to be considered.
The actuarial rate of interest, salary trend, pension trend and life expectancy are regarded as material assumptions. These parameters are shown in the following overview together with information on the parameter changes and their impact on the net present value calculation as of 31 December 2024.
| Thousands of Euros | |||
|---|---|---|---|
| Parameter change | Impact on the pension obligation |
||
| Rate of interest | Increase by 50 basis points | (5,386) | |
| Rate of interest | Decrease by 50 basis points | 5,957 | |
| Salary trend | Increase by 50 basis points | 93 | |
| Salary trend | Decrease by 50 basis points | (91) | |
| Pension trend | Increase by 100 basis points | 6,292 | |
| Pension trend | Decrease by 100 basis points | (5,360) | |
| Life expectancy | Increase by one year | 3,059 |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The impact on the net present value calculation as of 31 December 2023 is as follows:
| Thousands of Euros | |||
|---|---|---|---|
| Parameter change | Impact on the pension obligation |
||
| Rate of interest | Increase by 50 basis points | (5,411) | |
| Rate of interest | Decrease by 50 basis points | 5,510 | |
| Salary trend | Increase by 50 basis points | 159 | |
| Salary trend | Decrease by 50 basis points | (154) | |
| Pension trend | Increase by 100 basis points | 6,737 | |
| Pension trend | Decrease by 100 basis points | (5,729) | |
| Life expectancy | Increase by one year | 3,185 |
An amount of Euros 13,460 thousand (Euros 12,100 thousand at 31 December 2023) was recognized as an expense for defined contribution plans and is broken down as follows:
| Thousands of Euros | ||
|---|---|---|
| 31/12/2024 | 31/12/2023 | |
| Defined contribution plans of the Company | 35 | 38 |
| Employer contributions to statutory pension scheme | 13,425 | 12,062 |
| 13,460 | 12,100 |
This note provides information on the contractual conditions of the Group's financial liabilities, which are measured at amortized cost, except for the financial derivatives that are valued at fair value. For further information on exposure to interest rate risk, currency risk and liquidity risk and the fair values of financial liabilities, please refer to note 30.
Details at 31 December 2024 and 2023 are as follow:
| Thousands of Euros | ||||
|---|---|---|---|---|
| Financial liabilities | Reference | 31/12/2024 | 31/12/2023 | |
| Non-current bonds | (a) | 5,418,211 | 4,615,474 | |
| Senior secured debt | (b) | 2,373,264 | 3,309,032 | |
| Other loans | (b) | 53,125 | 445,249 | |
| Other non-current financial liabilities | (d) | 810,379 | 814,069 | |
| Non-current financial derivatives | Note 30 | — | 11 | |
| Non-current lease liabilities | Note 8 | 1,024,845 | 1,004,227 | |
| Loan transaction costs | (189,180) | (154,458) | ||
| Total non-current financial liabilities | 9,490,644 | 10,033,604 | ||
| Current bonds | (a) | 113,298 | 145,898 | |
| Senior secured debt | (b) | 25,420 | 34,832 | |
| Other loans | (b) | 292,780 | 699,211 | |
| Other current financial liabilities | (d) | 123,406 | 115,566 | |
| Current financial derivatives | Note 30 | 5,863 | 10,133 | |
| Current lease liabilities | Note 8 | 116,534 | 107,101 | |
| Loan transaction costs | (1,214) | (89,127) | ||
| Total current financial liabilities | 676,087 | 1,023,614 |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Detail of Senior Notes at 31 December 2024 is as follows:
| Thousands of Euros | ||||||||
|---|---|---|---|---|---|---|---|---|
| Issuance date | Company | Nominal value | Currency | Annual coupon | Maturity | |||
| Unsecured senior notes |
5/10/2021 (1) 5/10/2021 (1) |
Grifols, S.A. (2) Grifols, S.A. (2) |
1,400,000 705,000 |
Euros US Dollars |
3.875% 4.750% |
2028 2028 |
||
| 15/11/2019 (1) | Grifols, S.A. (2) | 770,000 | Euros | 2.250% | 2027 | |||
| Secured senior notes |
30/4/2024 (1) 4/6/2024 (1) |
Grifols, S.A. | 1,000,000 300,000 |
Euros | 7.500% | 2030 | ||
| 19/12/2024 (3) | Grifols, S.A. | 1,300,000 | Euros | 7.125% | 2030 |
(1) Listed on the Euronext Global Exchange Market of the Irish Stock Exchange (ISE)
(2) As a result of the merger between Grifols Escrow Issuer, S.A. and Grifols, S.A. in the fiscal year 2023 (see note 2).
(3) Currently in process of preparation of the documentation for the listing on the Euronext Global Exchange Market of the Irish Stock Exchange (ISE)
On April 30, 2024, Grifols, S.A. closed the issuance of senior secured corporate notes (Senior Secured Notes) amounting to Euros 1,000 million. Subsequently, on June 4, 2024, an additional private placement of senior secured notes amounting to Euros 300 million was completed. Both placements mature in May 2030 and bear an annual coupon of 7.5%, having the same economic terms and benefiting from the same personal garantees and in rem security as the senior secured notes issued on November 15, 2019. These notes have customary change of control protection in respect of the issuer. The funds obtained have been used to repay the senior unsecured notes ("Grifols Senior Unsecured Notes") maturing in May 2025 amounting Euros 1,000 million and to partially repay (for an amount of Euros 300 million) the Group's revolving credit facility of the Group's Credit and Guaranty Agreement originally dated November 15, 2019 (the "Credit Agreement") (note 21(b)).
On December 19, 2024, Grifols, S.A. closed the issuance of senior secured corporate notes (Senior Secured Notes) amounting Euros 1,300 million, maturing in May 2030 and bearing an annual coupon of 7.125%. These notes also have customary change of control protection and in addition they have an special redemption feature during the call protection period ("non-call period") allowing for a favorable redemption price versus the make-whole cost during such non-call period. The net funds obtained from such issuance have been used, together with available cash, to: (i) fully repay the Senior Secured Notes ("Senior Secured Notes") of Grifols, S.A. maturing in February 2025, for an amount of Euros 343 million; and (ii) fully clean-down the amount drawn under the revolving credit facility of the Credit Agreement (note 21(b)).
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Details of movement in the Senior Notes at a 31 December 2024 are as follows:
| Operating outstanding balance at 01/01/2024 |
Issuance | Cancellation | Exchange differences |
Operating outstanding balance at 31/12/2024 |
|||
|---|---|---|---|---|---|---|---|
| Senior unsecured corporate notes 2017 |
1,000,000 | — | (1,000,000) | — | — | ||
| Senior secured corporate notes 2019 |
1,577,465 | — | (837,856) | — | 739,609 | ||
| Senior unsecured corporate notes Euros 2021 |
1,400,000 | — | — | — | 1,400,000 | ||
| Senior unsecured corporate notes US Dollars 2021 |
638,009 | — | — | 40,593 | 678,602 | ||
| Senior secured corporate notes 2024 |
— | 2,600,000 | — | — | 2,600,000 | ||
| 4,615,474 | 2,600,000 | (1,837,856) | 40,593 | 5,418,211 |
Details of movement in the Senior Notes at 31 December 2023 are as follows:
| Thousands of Euros | |||||
|---|---|---|---|---|---|
| Operating outstanding balance at 01/01/2024 |
Exchange differences |
Operating outstanding balance at 31/12/2024 |
|||
| Senior unsecured corporate notes 2017 | 1,000,000 | — | 1,000,000 | ||
| Senior secured corporate notes 2019 | 1,577,465 | — | 1,577,465 | ||
| Senior unsecured corporate notes Euros 2021 | 1,400,000 | — | 1,400,000 | ||
| Senior unsecured corporate notes US Dollars 2021 | 660,979 | (22,970) | 638,009 | ||
| 4,638,444 | (22,970) | 4,615,474 |
At 31 December 2024 and 2023 the current obligations caption includes the issue of bearer promissory notes to Group employees, as follows:
| Thousands of Euros | |||
|---|---|---|---|
| 31/12/2024 | 31/12/2023 | ||
| Issuance date | 4/5/2024 | 5/5/2023 | |
| Maturity date | 4/5/2025 | 4/5/2024 | |
| Nominal amount of promissory notes (Euros) | 3,000 | 3,000 | |
| Interest rate | 5.00% | 4.00% | |
| Promissory Notes subscribed | 77,475 | 117,570 | |
| Buy-backs or redemptions | (3,084) | (1,842) | |
| Interest pending accrual | (1,214) | (1,540) |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Details of loans and borrowings at 31 December 2024 and 2023 are as follows:
| Date awarded | Maturity date | Thousands of Euros | ||||||
|---|---|---|---|---|---|---|---|---|
| Interest rate | 31/12/2024 | 31/12/2023 | ||||||
| Credit | Currency | Amount extended |
Carrying amount |
Amount extended |
Carrying amount |
|||
| Senior debt - Tranche B | Euros | Euribor + 2,25% | 15/11/2019 | 15/11/2027 | 1,360,000 | 856,869 | 1,360,000 | 1,242,210 |
| Senior debt - Tranche B | US Dollars | SOFR + 2,00% | 15/11/2019 | 15/11/2027 | 2,343,896 | 1,516,395 | 2,343,896 | 2,066,822 |
| Total senior debt | 3,703,896 | 2,373,264 | 3,703,896 | 3,309,032 | ||||
| EIB Loan | Euros | 2.40% | 20/11/2015 | 20/11/2025 | — | — | 100,000 | 10,625 |
| EIB Loan | Euros | 2.02% | 22/12/2017 | 22/12/2027 | 85,000 | 21,250 | 85,000 | 31,875 |
| EIB Loan | Euros | 2.15% | 25/9/2018 | 25/9/2028 | 85,000 | 31,875 | 85,000 | 42,500 |
| Total EIB Loan | 170,000 | 53,125 | 270,000 | 85,000 | ||||
| Revolving Credit | US Dollars | SOFR + 2,50% | 15/11/2019 | 15/11/2025 | 414,667 | — | 937,559 | 360,249 |
| Revolving Credit Renewed | US Dollars | SOFR + 2,50% | 19/12/2024 | 30/5/2027 | 863,500 | — | — | — |
| Total Revolving Credit | 1,278,167 | — | 937,559 | 360,249 | ||||
| Loan transaction costs | — | (88,257) | — | (104,797) | ||||
| Non-current loans and borrowings | 5,152,063 | 2,338,132 | 4,911,455 | 3,649,484 |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| Interest rate | Date awarded | Maturity date | Thousands of Euros | |||||
|---|---|---|---|---|---|---|---|---|
| Currency | 31/12/2024 | 31/12/2023 | ||||||
| Credit | Amount extended |
Carrying amount |
Amount extended |
Carrying amount |
||||
| Senior debt - Tranche B | Euros | Euribor + 2,25% | 15/11/2019 | 15/11/2027 | (*) | 7,830 | (*) | 13,076 |
| Senior debt - Tranche B | US Dollars | SOFR + 2,00% | 15/11/2019 | 15/11/2027 | (*) | 17,590 | (*) | 21,756 |
| Total senior debt | — | 25,420 | — | 34,832 | ||||
| EIB Loan | Euros | 2.40% | 20/11/2015 | 20/11/2025 | (*) | 10,625 | (*) | 10,625 |
| EIB Loan | Euros | 2.02% | 22/12/2017 | 22/12/2027 | (*) | 10,625 | (*) | 10,625 |
| EIB Loan | Euros | 2.15% | 25/9/2018 | 25/9/2028 | (*) | 10,625 | (*) | 10,625 |
| Total EIB Loan | — | 31,875 | — | 31,875 | ||||
| Other current loans | 0,10% - Euribor + 7,9% | 277,048 | 260,905 | 691,514 | 667,336 | |||
| Loan transaction costs | — | — | — | (59,735) | ||||
| Current loans and borrowings | 277,048 | 318,200 | 691,514 | 674,308 | ||||
(*) See amount granted under non-current debt.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Current loans and borrowings include accrued interest amounting to Euros 25,775 thousand at 31 December 2024 (Euros 27,468 thousand at 31 December 2023).
Between 2015 and 2018, the Group arranged three long-term loans with the European Investment Bank totaling Euros 270,000 thousand (divided into two loans of Euros 85,000 thousand and one loan of Euros 100,000 thousand) to support its investments in R&D, mainly focused on the search for new therapeutic indications for plasma-derived protein therapies. The financial terms include a fixed interest rate, a maturity of 10 years with a grace period of 2 years. At 31 December 2024 the carrying amount of the loans obtained from the European Investment Bank amounts to Euros 85,000 thousand (Euros 116,875 thousand at 31 December 2023).
"Other current loans" includes a secured loan from the Group company Biotest, AG with an original term of 5 years until 2024. The total volume amounts to Euros 240 million, divided into two Term Facilities (B1 and B2) of Euros 225 million and a Revolving Credit Facility of Euros 15 million. As of December 31, 2024, said loan has been fully repaid in accordance with its maturity (Euros 223,077 thousand at 31 December 2023).
Additionally, it is relevant to mention that the funds obtained from the sale transaction of Shanghai RAAS have been used to amortize, on a pro-rata basis, the Senior Debt Tranche B maturing in 2027 and the Senior Secured Bonds ("Senior Secured Notes") maturing in 2025. The prepayments were made towards next eight installments and the remainder was applied pro-rata against the remaining installments.
The Senior Secured debt consists of an eight-year loan divided into two tranches: US Tranche B and Tranche B in Euros. The terms and conditions of both tranches are as follows:
Details of Tranche B by maturity at 31 December 2024 are as follows:
| US Tranche B | Tranche B in Euros | ||||
|---|---|---|---|---|---|
| Currency | Principal in Thousands of US Dollars |
Principal in Thousands of Euros |
Currency | Principal in Thousands of Euros |
|
| Maturity | |||||
| 2026 | US Dollars | 8,431 | 8,115 | Euros | 4,582 |
| 2027 | US Dollars | 1,566,943 | 1,508,280 | Euros | 852,287 |
| Total | US Dollars | 1,575,374 | 1,516,395 | Euros | 856,869 |
The borrowers of the total Senior secured debt are Grifols, S.A. and Grifols Worldwide Operations USA, Inc.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
On 11 December 2024, and in relation to the Multicurrency Revolving Credit Facility (RCF), it was reported that the amount was increased from USD 1,000 million to USD 1,278.67 million until November 2025.
On 23 December 2024, and in relation to the Multicurrency Revolving Credit Facility (RCF), it was reported an 18 month extension of most of its current amount (the "RCF Extension"), with a new maturity in May 2027 and an amount of USD 863.50 million.
Following the extension of the Multicurrency Revolving Credit Facility (RCF), the financial expenses associated with the facility remain unchanged.
Movement in the Revolving Credit Facility is as follows:
| Thousands of Euros | ||||
|---|---|---|---|---|
| 31/12/2024 | 31/12/2023 | |||
| Drawn opening balance | 360,249 | — | ||
| Drawdowns | 1,340,285 | 1,501,207 | ||
| Repayments | (1,722,537) | (1,131,565) | ||
| Translation differences | 22,003 | (9,393) | ||
| Drawn closing balance | — | 360,249 |
On February 21, further commitments from banks amounting to USD 74.5 million were signed, increasing the RCF for an amount of 74.5 millions of US Dollars (see note 34).
The outstanding notes issuances and the Credit Agreement include customary restricted covenants, including the following:
As of December 31, 2024 and 2023, the Group is in compliance with the customary restricted covenants included in the financing agreements.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The notes and the senior secured debt under the Credit Agreement (including the revolving loans under the Credit Agreement) are guaranteed by Grifols, S.A. and certain significant subsidiaries of Grifols, S.A., which together with Grifols, S.A., represent, in the aggregate, at least 60% of the consolidated EBITDA of the Group. The guarantors are Grifols, S.A., Grifols Worldwide Operations Limited, Grifols Biologicals LLC, Grifols Shared Services North America, Inc., Grifols Therapeutics, LLC, Instituto Grifols, S.A., Grifols Worldwide Operations USA, Inc., Grifols USA, LLC, Grifols International, S.A. and Grifols Biotest Holdings GmbH.
Details of other financial liabilities at 31 December 2024 and 2023 are as follows:
| Thousands of Euros | ||||
|---|---|---|---|---|
| Other financial liabilities | Reference | 31/12/2024 | 31/12/2023 | |
| Non-current debt with GIC (sovereign wealth fund in Singapore) | (i) | 760,080 | 759,554 | |
| Non-current preferential loans | 5,613 | 5,966 | ||
| Other non-current financial liabilities | (ii) | 44,686 | 48,549 | |
| Total other non-current financial liabilities | 810,379 | 814,069 | ||
| Current debt with GIC (sovereign wealth fund in Singapore) | (i) | 84,539 | 81,384 | |
| Current preferential loans | 1,392 | 1,536 | ||
| Other current financial liabilities | 37,474 | 32,646 | ||
| Total other current financial liabilities | 123,405 | 115,566 |
In November 2021 approval was received from the pertinent authorities to close the agreement with GIC (Sovereign Fund of Singapore), announced in June 2021, whereby the Group received an amount of US Dollars 990 million in exchange for 10 ordinary Class B shares in Biomat USA and nine ordinary Class B shares in a new sub-holding, Biomat Newco, created for this purpose.
The main terms and conditions of the agreement with GIC were:
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
At 31 December 2024, current debt with GIC includes Euros 34,385 thousand of accrued interests plus Euros 50,154 thousand related to the share redemption right (Euros 34,230 thousand of accrued interests plus Euros 47,154 thousand related to the share redemption right at 31 December 2023).
Grifols did not have the discretional right to avoid payment in cash and therefore, the instrument is recorded as a financial liability.
The Group does not lose control of Biomat USA and continues overseeing all aspects of the Biomat Group's administration and operations.
At 31 December 2024, "Other non-current financial liabilities" include mainly an unsecured long-term loan in the amount of Euros 44.3 million corresponding to Biotest, AG, a company acquired by the Group on 25 April 2022 (note 3) (Euros 44.3 million and Euros 3.4 million from a supply contract respectively at 31 December 2023).
Details of the maturity of other financial liabilities are as follows:
| Thousands of Euros | ||||
|---|---|---|---|---|
| 31/12/2024 | 31/12/2023 | |||
| Maturity at: | ||||
| Up to one year | 123,405 | 115,566 | ||
| Two years | 51,645 | 52,268 | ||
| Three years | 51,211 | 48,478 | ||
| Four years | 51,016 | 48,060 | ||
| Five years | 95,262 | 47,848 | ||
| Over five years | 561,245 | 617,415 | ||
| 933,784 | 929,635 |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| Thousands of Euros | ||||||
|---|---|---|---|---|---|---|
| Reference | Bonds | Senior Secured debt & Other loans |
Finance lease liabilities |
Other financial liabilities |
Total | |
| Carrying amount at 1 January 2022 | 4,743,534 | 3,707,048 | 873,724 | 882,935 | 10,207,241 | |
| New financing | 112,557 | 990,537 | — | 16,448 | 1,119,542 | |
| Refunds | (217,058) | (944,386) | (104,287) | (15,685) | (1,281,416) | |
| Interest accrued | 176,317 | 206,901 | 43,640 | 84,586 | 511,444 | |
| Other movements | 744 | (744) | 123,792 | — | 123,792 | |
| Interest paid/received | (150,595) | (156,461) | — | (43,331) | (350,387) | |
| Business combinations | Note 3 | (1,804) | 121,597 | 30,290 | 31,016 | 181,099 |
| Foreign exchange differences | 27,965 | 117,029 | 49,785 | 50,154 | 244,933 | |
| Balance at 31 December 2022 | 4,691,660 | 4,041,521 | 1,016,944 | 1,006,123 | 10,756,248 | |
| New financing | 113,100 | 1,505,657 | — | 4,621 | 1,623,378 | |
| Refunds | (121,957) | (1,171,677) | (116,394) | (57,532) | (1,467,560) | |
| Interest accrued | 177,482 | 352,325 | 40,105 | 85,586 | 655,498 | |
| Other movements | — | — | 184,186 | 3,221 | 187,407 | |
| Interest paid/received | (147,998) | (308,048) | — | (72,896) | (528,942) | |
| Business combinations | Note 3 | — | — | — | 2,464 | 2,464 |
| Foreign exchange differences | (29,971) | (95,983) | (13,513) | (31,808) | (171,275) | |
| Balance at 31 December 2023 | 4,682,316 | 4,323,795 | 1,111,328 | 939,779 | 11,057,218 | |
| New financing (*) | 2,616,194 | 1,340,285 | — | (7,425) | 3,949,054 | |
| Refunds | (1,956,576) | (3,240,696) | (111,488) | (50,165) | (5,358,925) | |
| Interest accrued | 228,085 | 399,225 | 49,102 | 69,647 | 746,059 | |
| Other movements | — | — | 49,356 | 2,922 | 52,278 | |
| Interest paid/received | (182,007) | (317,148) | — | (72,332) | (571,487) | |
| Foreign exchange differences | 41,358 | 150,873 | 43,081 | 57,222 | 292,534 | |
| Balance at 31 December 2024 | 5,429,370 | 2,656,334 | 1,141,379 | 939,648 | 10,166,731 | |
| (*) Includes transaction costs |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Details are as follows:
| Thousands of Euros | |||
|---|---|---|---|
| 31/12/2024 | 31/12/2023 (*) | ||
| Suppliers | 852,305 | 822,953 | |
| VAT payable | 13,825 | 13,357 | |
| Taxation authorities, withholdings payable | 10,626 | 8,892 | |
| Social security payable | 42,692 | 28,180 | |
| Other public entities | 143,036 | 82,752 | |
| Other payables | 210,179 | 133,181 | |
| Current income tax liabilities | 60,535 | 14,523 | |
| 1,123,019 | 970,657 |
(*) Restated figures (note 2.d)
Details of balances with related parties are shown in note 31.
The Group's exposure to currency risk and liquidity risk associated with trade and other payables is described in note 30.
In accordance with the provision of Law 18/2022 that amends Law 15/2010 of 5 July, for fiscal years 2024 and 2023 information concerning the average payment period to suppliers is included.
Information concerning the average payment period to suppliers of Spanish companies is as follows:
| Days | |||
|---|---|---|---|
| 31/12/2024 | 31/12/2023 | ||
| Average payment period to suppliers | 70.87 | 70.87 | |
| Paid invoices ratio | 72.04 | 72.18 | |
| Outstanding invoices ratio | 59.57 | 62.85 | |
| Thousands of Euros | |||
|---|---|---|---|
| 31/12/2024 | 31/12/2023 | ||
| Total invoices paid | 815,222 | 684,906 | |
| Total outstanding invoices | 94,396 | 100,130 |
Information concerning invoices paid in a period of less than the maximum period established by the Law is as follows:
| 31/12/2024 | 31/12/2023 | |
|---|---|---|
| Monetary volume paid in euros (thousands of Euros) | 306,910 | 285,605 |
| Percentage of total monetary payments to suppliers | 37.65 % | 41.70 % |
| Number of paid invoices | 26,648 | 27,281 |
| Percentage of the total number of invoices paid to suppliers | 28.58 % | 29.91 % |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Details at 31 December are as follows:
| Thousands of Euros | ||
|---|---|---|
| 31/12/2024 | 31/12/2023 (*) | |
| Salaries payable | 240,650 | 237,099 |
| Other current debts | 6,912 | 7,074 |
| Deferred income | 36,500 | 28,870 |
| Advances received | 34,365 | 10,323 |
| Other current liabilities | 318,427 | 283,366 |
| (*) Restated figures (Note 2.d) |
At 31 December 2024 and 2023, the advances received are contract liabilities relate to unperformed performance obligations for which Grifols has received a consideration from the customer.
Net revenues are mainly generated from the sale of goods.
The distribution of net consolidated revenues for 2024, 2023 and 2022 by segment is as follows:
| Thousands of Euros | ||||
|---|---|---|---|---|
| 2024 | 2023 | 2022 | ||
| Biopharma | 6,142,588 | 5,558,301 | 5,005,382 | |
| Diagnostic | 644,898 | 670,269 | 671,292 | |
| Bio supplies | 215,664 | 159,957 | 146,076 | |
| Others | 209,232 | 203,450 | 250,165 | |
| Intersegments | — | — | (8,948) | |
| 7,212,382 | 6,591,977 | 6,063,967 |
The geographical distribution of net consolidated revenues is as follows:
| Thousands of Euros | ||||
|---|---|---|---|---|
| 2024 | 2023 | 2022 | ||
| USA and Canada | 4,087,030 | 3,898,961 | 3,855,607 | |
| Spain | 423,080 | 362,877 | 320,631 | |
| European Union | 1,118,258 | 893,050 | 711,579 | |
| Rest of the world | 1,584,014 | 1,437,089 | 1,176,150 | |
| Consolidated | 7,212,382 | 6,591,977 | 6,063,967 | |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Details of discounts and other reductions in gross revenue are as follows:
| Thousands of Euros | |||||
|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | |||
| Gross sales | 9,489,669 | 8,389,387 | 7,720,463 | ||
| Chargebacks | (1,891,578) | (1,525,210) | (1,402,218) | ||
| Cash discounts | (93,024) | (81,773) | (76,547) | ||
| Volume rebates | (76,312) | (59,000) | (66,280) | ||
| Medicare and Medicaid | (72,398) | (68,353) | (64,438) | ||
| Other discounts | (143,975) | (63,074) | (47,013) | ||
| Net sales | 7,212,382 | 6,591,977 | 6,063,967 |
Movement in discounts and other reductions in gross revenue during 2024 is as follows:
| Thousands of Euros | ||||||
|---|---|---|---|---|---|---|
| Chargebacks | Cash discounts |
Volume rebates |
Medicare / Medicaid |
Other discounts |
Total | |
| Balance at 31 December 2023 | 318,559 | 7,009 | 23,528 | 26,365 | 34,792 | 410,253 |
| Current estimate related to sales made in current and previous periods (1) |
1,891,578 | 93,024 | 76,312 | 72,398 | 143,975 | 2,277,287 |
| (Actual returns or credits in current period related to sales made in current period) (2) |
(1,737,477) | (85,100) | (37,569) | (56,470) | (86,765) (2,003,381) | |
| (Actual returns or credits in current period related to sales made in prior periods) (3) |
(105,282) | (7,473) | (23,237) | (18,404) | 10,322 | (144,074) |
| Translation differences | 18,281 | (640) | 1,946 | 1,567 | (594) | 20,560 |
| Balance at 31 December 2024 | 385,659 | 6,820 | 40,980 | 25,456 | 101,730 | 560,645 |
(1) Net impact in the Consolidated Statements of Profit and Loss: estimate for the current year plus prior years' adjustments. Adjustments made during the year corresponding to prior years' estimates have not been significant.
(2) Amounts credited and posted against provisions for current period
(3) Amounts credited and posted against provisions for prior period
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Movement in discounts and other reductions to gross revenue during 2023 was as follows:
| Thousands of Euros | ||||||
|---|---|---|---|---|---|---|
| Chargebacks | Cash discounts |
Volume rebates |
Medicare / Medicaid |
Other discounts |
Total | |
| Balance at 31 December 2022 | 264,513 | 6,184 | 23,565 | 27,036 | 25,983 | 347,281 |
| Current estimate related to sales made in current and previous periods (1) |
1,525,210 | 81,773 | 59,000 | 68,353 | 63,074 | 1,797,410 |
| (Actual returns or credits in current period related to sales made in current period) (2) |
(1,324,855) | (74,829) | (37,078) | (49,402) | (30,647) (1,516,811) | |
| (Actual returns or credits in current period related to sales made in prior periods) (3) |
(135,606) | (6,443) | (21,182) | (18,676) | (23,374) | (205,281) |
| Translation differences | (10,703) | 324 | (777) | (946) | (244) | (12,346) |
| Balance at 31 December 2023 | 318,559 | 7,009 | 23,528 | 26,365 | 34,792 | 410,253 |
Movement in discounts and other reductions to gross revenue during 2022 was as follows:
| Thousands of Euros | ||||||
|---|---|---|---|---|---|---|
| Chargebacks | Cash discounts |
Volume rebates |
Medicare / Medicaid |
Other discounts |
Total | |
| Balance at 31 December 2021 | 159,846 | 5,701 | 21,246 | 25,614 | 10,585 | 222,992 |
| Current estimate related to sales made in current and previous periods (1) |
1,402,218 | 76,547 | 66,280 | 64,438 | 47,013 | 1,656,496 |
| (Actual returns or credits in current period related to sales made in current period) (2) |
(1,196,670) | (69,960) | (43,494) | (43,332) | (28,818) | (1,382,274) |
| (Actual returns or credits in current period related to sales made in prior periods) (3) |
(109,726) | (6,442) | (21,501) | (21,271) | (2,935) | (161,875) |
| Translation differences | 8,845 | 338 | 1,034 | 1,587 | 138 | 11,942 |
| Balance at 31 December 2022 | 264,513 | 6,184 | 23,565 | 27,036 | 25,983 | 347,281 |
Details of personnel expenses by function are as follows:
| Thousands of Euros | ||||
|---|---|---|---|---|
| 2024 | 2023 (*) | 2022 (*) | ||
| Cost of sales | 1,373,499 | 1,384,426 | 1,367,923 | |
| Research and development | 181,270 | 172,970 | 159,766 | |
| Selling, general & administration expenses | 497,918 | 528,784 | 472,413 | |
| 2,052,687 | 2,086,180 | 2,000,102 |
(*) Restated figures (Note 2.d)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Details by nature are as follows:
| Thousands of Euros | |||||
|---|---|---|---|---|---|
| 2024 | 2023 (*) | 2022 (*) | |||
| Wages and salaries | 1,668,348 | 1,698,415 | 1,621,294 | ||
| Contributions to pension plans | 42,644 | 42,843 | 41,156 | ||
| Other social charges | 33,994 | 30,868 | 33,678 | ||
| Social Security | 307,701 | 314,054 | 303,974 | ||
| 2,052,687 | 2,086,180 | 2,000,102 |
(*) Restated figures (Note 2.d)
On February 15, 2023, the Group announced the implementation of a comprehensive operational improvement plan with significant savings. The plan included the optimization of plasma costs and operations, the streamlining of corporate functions, and other initiatives to improve efficiency in the organization. It also included a reduction in staff in 2023 that affected approximately 8% of the human team, mainly in plasma operations in the United States. During the year 2024, the Group have recognized a severance expense of Euros 14,232 thousand (Euros 75,348 thousand during the year 2023).
The average headcount during 2024 and 2023, by department, was approximately as follows:
| Average headcount | |||
|---|---|---|---|
| 2024 | 2023 | ||
| Manufacturing | 17,472 | 17,641 | |
| R&D - technical area | 1,252 | 1,226 | |
| Administration and others | 1,630 | 1,697 | |
| General management | 248 | 242 | |
| Marketing | 167 | 159 | |
| Sales and Distribution | 1,375 | 1,414 | |
| 22,144 | 22,379 |
The headcount of the Group employees and the Company's Directors at 31 December 2024 by gender, is as follows:
| 31/12/2024 | ||||
|---|---|---|---|---|
| Man | Women | Undeclared | Total Number of Employees |
|
| Administrators | 9 | 4 | — | 13 |
| Manufacturing | 7,788 | 10,930 | 56 | 18,774 |
| Research&development - technical area | 531 | 981 | 2 | 1,514 |
| Administration and others | 992 | 681 | — | 1,673 |
| General management | 130 | 149 | — | 279 |
| Marketing | 67 | 117 | — | 184 |
| Sales and Distribution | 712 | 684 | — | 1,396 |
| 10,229 | 13,546 | 58 | 23,833 |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The breakdown of employees who are part of the Senior Management is as follows:
The headcount of the Group employees and the Company's directors at 31 December 2023 by gender, was as follows:
| 31/12/2023 | ||||
|---|---|---|---|---|
| Man | Women | Undeclared | Total Number of Employees |
|
| Administrators | 7 | 4 | — | 11 |
| Manufacturing | 7,650 | 11,272 | 57 | 18,979 |
| Research&development - technical area | 478 | 776 | 1 | 1,255 |
| Administration and others | 1,018 | 668 | — | 1,686 |
| General management | 125 | 138 | — | 263 |
| Marketing | 55 | 100 | — | 155 |
| Sales and Distribution | 709 | 685 | 1 | 1,395 |
| 10,042 | 13,643 | 59 | 23,744 |
The breakdown of employees who are part of the Senior Management is as follows:
Expenses for the amortization and depreciation of intangible assets, right of use assets and property, plant and equipment, incurred during 2024, 2023 and 2022 classified by functions are as follows:
| Thousands of Euros | |||
|---|---|---|---|
| 2024 | 2023 (*) | 2022 (*) | |
| Cost of sales | 273,306 | 274,552 | 278,628 |
| Research and development | 53,311 | 64,731 | 44,295 |
| Selling, general & administration expenses | 111,280 | 107,139 | 88,057 |
| 437,897 | 446,422 | 410,980 |
(*) Restated figures (Note 2.d)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Other operating income and expenses incurred during 2024, 2023 and 2022 by function are as follows:
| Thousands of Euros | ||||
|---|---|---|---|---|
| 2024 | 2023 (*) | 2022 (*) | ||
| Cost of sales | 618,695 | 621,119 | 700,749 | |
| Research and development | 192,877 | 168,358 | 164,229 | |
| Selling, general & administration expenses | 712,137 | 798,720 | 584,489 | |
| 1,523,709 | 1,588,197 | 1,449,467 |
(*) Restated figures (Note 2.d)
Details by nature are as follows:
| Reference | Thousands of Euros | |||
|---|---|---|---|---|
| 2024 | 2023 (*) | 2022 (*) | ||
| Changes in trade provisions | (21,007) | 3,567 | 8,743 | |
| Professional services | 379,903 | 424,332 | 307,385 | |
| Commissions | 28,494 | 44,946 | 40,397 | |
| Supplies and auxiliary materials | 194,672 | 210,489 | 254,344 | |
| Operating leases | Note 8 | 47,122 | 44,038 | 39,676 |
| Freight | 186,017 | 187,693 | 191,360 | |
| Repair and maintenance expenses | 269,843 | 243,362 | 223,970 | |
| Advertising | 83,901 | 80,223 | 91,887 | |
| Insurance | 49,242 | 50,971 | 46,809 | |
| Royalties | 21,817 | 21,766 | 13,646 | |
| Travel expenses | 43,883 | 48,119 | 52,606 | |
| External services | 106,121 | 98,876 | 89,799 | |
| R&D Expenses | 108,227 | 98,947 | 94,903 | |
| Gains on disposal of assets | — | (3,042) | (22,236) | |
| Other | 25,474 | 33,910 | 16,178 | |
| Other operating income&expenses | 1,523,709 | 1,588,197 | 1,449,467 | |
| (*) Restated figures (Note 2.d) |
On February 15, 2023, the Group announced the implementation of a comprehensive operational improvement plan with significant savings. The plan included the optimization of plasma costs and operations, the streamlining of corporate functions, and other initiatives to improve efficiency in the organization. As of 31 December 2024, the Group recognized an expense of approximately Euros 22,302 thousand (Euros 79,090 thousand at 31 December 2023) mainly in professional services.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Details are as follows:
| Thousands of Euros | ||||
|---|---|---|---|---|
| Reference | 2,024 | 2023 (*) | 2,022 | |
| Finance income | 44,423 | 62,429 | 33,859 | |
| Finance costs from Senior Unsecured Notes | (230,478) | (177,482) | (181,149) | |
| Finance costs from senior debt | Note 21(b) | (279,543) | (257,350) | (161,466) |
| Finance costs from other financial liabilities | (69,452) | (73,533) | (81,914) | |
| Capitalized interest | Note 9 | 27,772 | 36,892 | 25,184 |
| Finance lease expenses | Note 8 | (50,870) | (44,587) | (45,198) |
| Other finance costs | (112,194) | (80,823) | (33,780) | |
| Finance costs | (714,765) | (596,883) | (478,323) | |
| Dividends | 2,060 | — | — | |
| Financial cost of sale of trade receivables | Note 15 | (30,782) | (24,993) | (18,201) |
| Change in fair value of financial instruments | Note 12 | 19,882 | 1,459 | 11,999 |
| Impairment of financial assets | (9,081) | — | — | |
| Exchange differences | (59,756) | (16,386) | 7,725 | |
| Finance result | (740,998) | (574,374) | (442,941) | |
| (*) Restated figures (Note 2.d) |
During 2024, the heading Finance costs from Senior Unsecured Notes includes financial expenses arising from the interest corresponding to senior secured bonds with a principal amount of Euros 1.300 millions issued at 7.5% that were used to amortize senior unsecured bonds with a principal amount of Euros 1.000 millions and an interest of 3.2% per annum.
The finance costs from other financial liabilities heading for 2024 includes finance costs related to the interest on the funds received by GIC amounting Euros 69,452 thousand (Euros 73,533 thousand at 31 December 2023) (see note 21(d)).
During 2024, the Group has capitalized interest at a rate of between 6.88% and 7.38% based on the financing received (between 6.03% and 6.79% during 2023).
Grifols, S.A. is authorized to file consolidated tax returns in Spain with Grifols Movaco, S.A., Laboratorios Grifols, S.A., Instituto Grifols, S.A., Biomat, S.A., Grifols Viajes, S.A., Grifols International, S.A., Grifols Engineering, S.A., Araclon Biotech and Aigües Minerals de Vilajuiga, S.A. Grifols, S.A., in its capacity as Parent, is responsible for the filing and settlement of the consolidated tax return. Under prevailing tax law, Spanish companies pay 25% tax, which may be reduced by certain deductions.
The North American company Grifols Shared Services North America, Inc. is also authorized to file consolidated tax returns in the USA with Grifols Biologicals Inc., Grifols USA, LLC., Biomat USA, Inc. and Grifols Therapeutics Inc. The profits of the companies domiciled in the USA, determined in accordance with prevailing tax legislation, are subject to tax of approximately 22% of taxable income, which may be reduced by certain deductions.
In 2021, the OECD released the Model Rules for Pillar 2 to address tax challenges arising from the digitization of the economy. This international tax system reform focuses on the geographic allocation of profits for tax purposes and is designed to ensure that multinational enterprises are subject to a minimum effective tax rate of 15%.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
On 15 December 2022, the Council of the European Union formally adopted the European Directive on Pillar 2. As of 31 December 2024 Spain has approved the Draft Law transposing the European Directive to ensure a global minimum taxation of 15% for multinational corporations. This legislation will apply prospectively to accounting periods beginning on January 1, 2024.
On 23 May 2023, the International Accounting Standards Board (IASB) published the International Tax Reform - Second Pillar Model Rules. Proposed amendments to IAS 12, which will be applicable for periods beginning on 1 January 2023. The amendments to IAS 12 provide for a mandatory temporary exemption in recognizing deferred tax balances arising from the implementation of Pillar 2 legislation.
The Group has developed an accounting policy consistent with the amendments to IAS 12, whereby the Group does not record adjustments to deferred tax assets and liabilities resulting from the introduction of the minimum effective tax rate of 15%. In developing this accounting policy, the Group has also adopted the exemption to avoid providing detailed information on the amendments for transitional periods beginning on January 1, 2023.
On 18 January 2024, the Constitutional Court declared unconstitutional various tax precepts contained in Royal Decree-Law 3/2016. The company has assessed the impact that these provisions had in 2017 and subsequent years, and considers that, as they did not have a significant impact, it will not challenge the tax assessments for these years.
Details of the income tax expense and income tax related to profit for the year are as follows:
| Thousands of Euros | |||
|---|---|---|---|
| 2,024 | 2,023 (*) | 2,022 (*) | |
| Profit before income tax from continuing operations | 443,996 | 207,021 | 338,013 |
| Tax at 25% | 110,999 | 51,755 | 84,503 |
| Permanent differences | 66,715 | (66,322) | (30,796) |
| Effect of different tax rates | (49,120) | 52,372 | 9,953 |
| Tax credits (deductions) | (21,991) | (1,193) | 3,667 |
| Prior year income tax expense | 16,698 | 2,132 | 12,685 |
| Other income tax expenses/(income) | 107,889 | 4,604 | 10,099 |
| Total income tax expense | 231,190 | 43,348 | 90,111 |
| Deferred tax | (75,067) | (140,095) | (15,138) |
| Current tax | 306,257 | 183,443 | 105,249 |
| Total income tax expense | 231,190 | 43,348 | 90,111 |
| (*) Restated figures (Note 2.d) |
The effect of the different tax rates is basically due to a change of country mix in profits.
As of December 31, 2024, the caption "Other income tax expenses/(income)" includes, among other concepts, the accrual of fiscal provisions (see Note 28(c)).
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Details of deferred tax assets and liabilities are as follows:
| Thousands of Euros | |||||
|---|---|---|---|---|---|
| Tax effect | |||||
| 31/12/2024 | 31/12/2023 | 31/12/2022 | |||
| Assets | |||||
| Provisions | 31,444 | 29,663 | 20,511 | ||
| Inventories | 76,368 | 73,661 | 67,557 | ||
| Tax credits (deductions) | 26,681 | 76,603 | 33,921 | ||
| Tax loss carryforwards | 49,664 | 27,804 | 58,159 | ||
| Fixed assets, amortisation and depreciation | 78,348 | 61,479 | — | ||
| Other | 90,872 | 44,735 | 6,197 | ||
| Subtotal, assets | 353,377 | 313,945 | 186,345 | ||
| Goodwill | (2,027) | (2,727) | (3,063) | ||
| Fixed assets, amortisation and depreciation | (9,677) | (4,155) | (16) | ||
| Intangible assets | — | — | (1,349) | ||
| Other | — | (6,734) | (6,994) | ||
| Subtotal, net liabilities | (11,704) | (13,616) | (11,422) | ||
| Deferred assets, net | 341,673 | 300,329 | 174,923 | ||
| Liabilities | |||||
| Goodwill | (451,387) | (376,520) | (337,948) | ||
| Intangible assets | (678,833) | (658,099) | (669,316) | ||
| Fixed assets | (74,625) | (85,082) | (92,811) | ||
| Debt cancellation costs | (56,811) | (41,894) | (50,666) | ||
| Others | (6,300) | (53,503) | — | ||
| Subtotal, liabilities | (1,267,956) | (1,215,098) | (1,150,741) | ||
| Tax loss carryforwards | 3,101 | 10,459 | 2,993 | ||
| Tax credits (deductions) | 18,259 | 68,104 | 14,578 | ||
| Inventories | 1,904 | 1,848 | 652 | ||
| Provisions | 123,880 | 105,656 | 70,206 | ||
| Other | 109,108 | 40,402 | 27,489 | ||
| Subtotal, net assets | 256,252 | 226,469 | 115,918 | ||
| Net deferred Liabilities | (1,011,704) | (988,629) | (1,034,823) |
Movement in deferred tax assets and liabilities is as follows: (Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| Thousands of Euros | ||||
|---|---|---|---|---|
| Deferred tax assets and liabilities | 31/12/2024 | 31/12/2023 | 31/12/2022 | |
| Balance at 1 January | (688,300) | (859,900) | (481,477) | |
| Movements during the year | 75,067 | 140,095 | 15,138 | |
| Business combination (note 3) | — | 239 | (361,051) | |
| Translation differences | (56,798) | 31,266 | (32,510) | |
| Balance at 31 December | (670,031) | (688,300) | (859,900) |
The Spanish companies have opted to apply accelerated depreciation to certain additions to property, plant and equipment, which has resulted in the corresponding deferred tax liability.
The remaining assets and liabilities recognized in 2024, 2023 and 2022 were recognized in the statement of profit and loss.
The majority of the tax deductions pending application from Spanish companies related mainly to research and development, mature in 18 years. Likewise, the Group estimates that practically the entire amount will be applied in five years.
The Group has not recognized as deferred tax assets the tax effect of the unused tax loss carryforwards of Group companies, which amount to Euros 125,153 thousand (Euros 103,303 thousand at 31 December 2023).
The amount of unrecognized deferred tax liabilities associated with investments in subsidiaries amounted to Euros 79,551 thousand as of 31 December 2024 (Euros 76,348 thousand as of 31 December 2023).
The commitments from Spanish companies from the reversal of deferred tax related to provisions of investments in subsidiaries are not significant.
As established by current legislation, taxes cannot be considered definitively settled until the returns have been audited by the corresponding tax authorities, or the statute of limitations has elapsed.
The Group is currently undergoing the tax audits explained below. Note that the Group acts with the tax authorities in a cooperative and transparent manner to resolve disputes and considers that its position in the years and matters described below is in accordance with the law and is based on a reasonable interpretation of the applicable regulations. Therefore, the Group intends to file all the appropriate appeals and petitions to best defend its interests.
• Certain companies of the Group domiciled in Spain, taxed under the Spanish tax consolidation regime, were subject to an audit by the Spanish State Tax Administration Agency in relation to Corporate Income Tax for the fiscal years 2014, 2015 and 2016 and Value Added Tax for the years 2015 and 2016.
On 8 November 2021, the Group agreed to the resulting assessments ("conformidad"). No penalties were imposed on any of the Group companies for any of the taxes subject to audit.
Moreover and since these assessments have resulted in an adjustment in the allocation of taxable income between different jurisdictions and in light of their effect on the Group's transfer pricing position, the Group now has a legal right to recover certain amounts from the corresponding countries jurisdictions, under a Mutual Agreement Procedure in accordance with the provisions of the European Convention on the elimination of double taxation in connection with the adjustment of profits from Group companies.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
• Grifols Shared Services North America, Inc. and subsidiaries received in 2020 notification of a tax audit relating to the State Income Tax for the fiscal years 2017 and 2018.
The US Internal Revenue Service ("IRS") has indicated that it intends to review the pricing of certain cross-border intercompany transactions involving the US. Currently, the IRS is still in the initial phase of their analysis and only beginning discussions have taken place.
• Certain Group companies domiciled in Spain, taxed under the Spanish tax consolidation regime, recently underwent an audit by the Spanish State Tax Administration Agency, in relation to Corporate Income Tax for the fiscal years 2017 to 2019 and Value Added Tax, personal income tax, non-resident income and capital income tax for June 2018 to December 2019. The Group disagreed to the corresponding assessment proposals ("disconformidad") and has received the corresponding final assessments. No penalties were imposed on any of the Group companies for any of the taxes subject to these audit proceedings.
As regards Corporate Income Tax, the assessment is based on a different pricing criteria approach. In relation to VAT, the assessment relies on a different interpretation of the financial activity carried out by the Group and how such difference affects the deductibility of certain expenses.
The net tax liability included in the group's Financial Statements to cover the worldwide exposure to uncertain tax treatments at December 31, 2024 is Euros 136,705 thousand (Euros 76,604 thousand as of December 31, 2023) and it is included under the caption "Other public entities". This increase in the net tax liability for uncertain tax positions relates to transfer pricing mainly as a result of an update of potential tax liabilities following the tax audits mentioned above.
Transfer pricing matters are complex, highly subjective and open to disputes involving different tax jurisdictions. The topics under discussion are complex and may take many years to resolve. The tax liability includes uncertain tax treatments that are estimated using either the most likely amount method or the expected value method and depend on the Group's assessment as to whether the approach taken by the Tax Authorities is likely to be sustained by Tribunals or Courts. Such assessment could change in the future to reflect progress in Tax Authorities' reviews to the extent that any Tax Authority review is concluded; progress in on-going appeals and international procedures, including the return of taxes which have already been paid under the assessments set out above; changes in legal provisions or in the interpretation of such provisions; or even expiry of the corresponding statutory periods of limitations.
Management believes that it is unlikely that additional liabilities, above the amounts provided, will arise. Also, it is possible that the amounts provided may change and be partially, or even entirely, mitigated in future periods, as reviews, appeals or procedures challenging the Tax Authorities' approach progress or even the relevant statutes of limitation expire. Management continues to believe that the Group's position on all its transfer pricing, audits and disputes is robust, and that the Group has recognised appropriate tax provision balances, including consideration of whether corresponding relief will be available under applicable Mutual Agreement Procedures with the different countries.
As highlighted above, the Group is currently under tax audit in several countries and the timing of any resolution of these audits is uncertain.
It is anticipated that tax payments may be required in relation to the ongoing tax audits which may be resolved over coming years. The Group considers the tax liabilities set out above to appropriately reflect, according to current information, the expected value of any final settlement. Some of the items discussed above are not currently within the scope of tax authority audits and may take longer to be resolved.
As at December 31, 2024, the Group continues to assess the implications of the OECD's Pillar 2 reform, which provide for global minimum taxation rules. These rules have been adopted in the EU through the relevant Directive, which Member States must transpose for the rules to apply as of 1 January 2024.
Beyond a significant increase in formal compliance burdens, the Group does not expect significant economic impacts from the application of this new regulation, as it is already subject to effective tax rates above 15% in most of the territories in which it operates and expects to benefit from the "transitional safe harbour" which allows avoiding the additional tax and alleviating formal compliance burdens.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
An exception to the above is Ireland, which has a nominal corporate income tax rate of 12.5% and has already passed its own Pillar 2 legislation which will allow it to levy corporate income tax directly. Although the complexity of the legislation could, in specific cases, give rise to additional taxation, the Group has made an assessment of such impact for 2024 and it amounts to Euros 5 million.
The Group has no significant guarantees extended to third parties.
Since 30 June 2023, Grifols, through Grifols Shared Services North America, Inc, acts as a guarantor for five lease contracts for certain ImmunoTek plasma centers not affected by the collaboration under Biotek America LLC. In addition, Grifols, S.A. acts as guarantor of the commitments made for the purchase of the 28 plasma centers (see note 11).
Additionally, the Group has significant guarantees extended to third parties described in note 19 and 21.
The Group's annual contribution to defined contribution pension plans of Spanish Group companies for 2024 has amounted to Euros 1,259 thousand (Euros 1,079 thousand for 2023).
In the event that control is taken of the Company, the Group has agreements with 31 employees/directors whereby they can unilaterally rescind their employment contracts with the Company and are entitled to termination benefits ranging from one to five years' salary.
In addition, the share-based remuneration plans maintained by the Company for certain employees include clauses according to which, in the event of a change of control, the amounts pending exchange would be early settled under the terms described in said agreements.
The Group has contracts with 23 executives entitling them to termination benefits ranging from one to four years of their salary in different circumstances.
In March 2022, the Group established a Restricted Stock Share Plan (hereinafter RSU) for certain employees. Under this plan, an employee may elect to receive up to 50% of his or her annual bonus in Class B non-voting ordinary shares (Grifols Class B Shares) or Grifols American Depositary Shares (Grifols ADSs), and the Group will match this with an additional 50% contribution in RSUs.
Class B Grifols shares and Grifols ADSs are valued at the date of grant of the bonus.
These RSUs will have a vesting period of 2 years and 1 day and will subsequently be exchanged for Grifols Class B Shares or Grifols ADSs (American Depositary Shares representing 1 Class B Share).
If an eligible employee leaves the company or is terminated prior to the vesting period, he/she will not be entitled to the additional RSUs.
At 31 December 2024, the Group has settled the 2022 RSU plan for an amount of Euros 17,577 thousand (Euros 3,296 thousand at 31 December 2023 corresponding to the 2020 RSU plan).
This commitment was treated as equity-settled, with no accumulated amount recognized at 31 December 2024 (Euros 8,282 thousand at 31 December 2023).
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
In May 2023, the Board of Directors approved a proposal to the Ordinary General Meeting on 16 June, 2023, which approved it, a long term incentive plan. based on the granting of stock options for certain executive directors, members of the senior management of Grifols and its subsidiaries. The plan has a term of four years for each beneficiary, from the effective date where 40% of the options granted will vest (provided that the conditions for their vesting are met) at the end of the second year of the plan and the remaining 60% will vest (provided that the conditions for their vesting are met) at the end of the fourth year of the plan. A maximum of 4,000,000 stock options will be granted, representing the right to acquire 4,000,000 Class A shares of the Company with an exercise price of Euros 8.96 per Class A share. As a condition for the vesting of the options granted, each beneficiary must have remained continuously employed by Grifols on each vesting date, must pass an individual performance evaluation and, in addition, settlement is subject to the achievement of specific, predetermined and quantifiable objectives, related to financial and non-financial metrics, in order to reward value creation through the achievement of the objectives set in the plan. The Company will allocate the shares it currently holds in treasury or may come to hold to cover the needs of the plan.
| Settlement date | Number of shares assigned | Unit fair value (Euros) |
|---|---|---|
| 2025 | 1,040,000 | 3.05 |
| 2027 | 1,560,000 | 2.85 |
Additionally, there is a special remuneration plan referenced to the value of the share settled in equity instruments for certain executives with an exercise price of Euros 8.964 and Euros 12.84 per Class A share and maturity 2024 and 2025.
| Settlement date | Number of shares assigned | Unit fair value (Euros) |
|---|---|---|
| 31/12/2026 | 180,000 | 2.39 |
| 22/2/2025 | 700,000 | 1.08 |
| 28/2/2025 | 270,000 | 2.19 |
The recognized amount in Equity as 31 December 2024 amounts to Euros 5,621 thousand (Euros 2,586 thousand at 31 December 2023).
In May 2023, the Board of Directors of Grifols, S.A. approved a new long-term incentive plan based on restricted stock units (RSUs) aimed at certain members of the management team of the Company and its subsidiaries. The plan has a total duration of four years, where 50% of the RSUs granted will be settled at the end of the second year of the plan and the remainder at the end of the fourth year of the plan. As a condition for the vesting of the RSUs granted, each beneficiary must have remained continuously employed by Grifols on the settlement date of the plan and, in addition, such settlement is subject to the achievement of performance objectives. The RSUs will be settled in cash for an amount equivalent to the average price of the Class A shares during the five (5) business days prior to the settlement. At 31 December 2024, the total accumulated amount is Euros 2.932 thousand. Of the total, 2,090 thousand euros are shortterm in the heading "Trade creditors and other accounts payable" (1,724 thousand euros as of December 31, 2023) and 842 thousand euros are long-term in the heading "Provisions" (without amount as of December 31, 2023). The amount recognized in the Consolidated Statement of Profit and Loss as of 31 December 2024 amounts to Euros 1,208 thousand (Euros 1,724 thousand in 2023).
| Settlement date | Number of RSUs assigned | Unit fair value (Euros) |
|---|---|---|
| 2025 | 268,350 | 9.44 |
| 2027 | 268,350 | 7.61 |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
In 2024, the Group has signed contracts with certain executives, establishing a long-term share-based or cash-based incentive as part of its remuneration system. In the case of transfer of shares, these will be made in equal terms on the anniversary date or at the end of the period, according to the terms of the agreement, and always subject to the permanence of the beneficiary on the agreed settlement dates. Each beneficiary must have been continuously employed by Grifols until the settlement date.
The amount recognized in equity as of December 31, 2024 amounts to Euros 1,058 to thousands.
The Group has a defined contribution plan (savings plan), which qualifies as a deferred salary arrangement under Section 401 (k) of the Internal Revenue Code (IRC). Once eligible, employees may elect to contribute a portion of their salaries to the savings plan, subject to certain limitations. The Group matches 100% of the first 4% of employee contributions and 50% of the next 2%. Group and employee contributions are fully vested when contributed. The total cost of matching contributions to the savings plan was US Dollars 33,6 million in 2024 (US Dollars 33.4 million in 2023).
The Group has a defined benefit pension plan for certain former Talecris Biotherapeutics, GmbH employees in Germany as required by statutory law. The pension cost relating to this plan is not material for the periods presented.
The Biotest Group has established retirement benefits and employment commitments for certain employees, primarily from its German companies. These benefits are based on employees' length of service and salary. The pension plans are voluntary and are not subject to statutory or legal obligations. The amount of pension liabilities largely depends on fluctuations in interest rates and the life expectancy of the beneficiaries.
Details of the Group's raw material purchase commitments at 31 December 2024 are as follows:
| Thousands of Euros | |||||
|---|---|---|---|---|---|
| 2025 334,304 |
|||||
| 2026 198,644 |
|||||
| 2027 128,568 |
|||||
| 2028 113,570 |
|||||
| 2029 112,946 |
|||||
| More than 5 years 128 |
|||||
Pursuant to the share purchase agreement dated 28 December 2018, the Grifols Group, through Grifols Shares Services North America Inc (for the shares of BPC Plasma Inc, formerly known as Biotest US Corporation ("BPC") and Grifols Worldwide Operations Limited (for the shares of Haema AG, now called Haema GmbH ("Haema")) (the "Selling Companies") sold 100% of the capital shares of BPC and Haema to Scranton Plasma B.V. ("Scranton"). The share purchase agreement includes an option for the Selling Companies to repurchase the shares, granting the Selling Companies an irrevocable and exclusive right (though not an obligation) to repurchase the shares sold to Scranton at any time following the sale, provided that when the option of the repurchase of the shares of a company (BPC or Haema, as the case may be) is exercise, the option for the repurchase of the other company (Haema or BPC, as the case may be) is also exercised simultaneously.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The purchase option involves a fluctuating number of shares and a variable acquisition price. This characteristic classifies it as a derivative financial instrument that needs to be fairly valued, ultimately impacting the profit and loss account.
The exercise price for the option will be determined based on the higher of the following two amounts: (i) the aggregate of the price at which the shares were sold to Scranton, increased by any expenses relating to the completion of the transactions contemplated in the relevant share purchase agreement, plus the increase in net working capital from the date of sale until the repurchase completion date resulting from the exercise of the repurchase option; and (ii) the amount required to pay in full the indebtedness that Scranton incurred with the lending entity to purchase the shares of Haema and BPC from the Selling Companies, for an amount of USD 425,000,000 along with any accrued interest and additional amounts required to fully repay that indebtedness.
Based on the abovementioned contractual conditions, Grifols has estimated the value of the exercise of the repurchase option as follows: (i) the price at which the Selling Companies sold the shares to Scranton (totalling USD538,000,000) increased by any expenses relating to the completion of the transactions contemplated in the relevant share purchase agreement, plus (ii) the change in working capital. Based on the business models of Haema and BPC, this change in working capital is expected to primarily reflect the undistributed profits at the time of exercise of the repurchase option. Given that the price of the exercise of the repurchase option aligns closely with the fair value of BPC and Haema, this option's overall value is not considered significant. Furthermore, since the valuation of the option relies on unobservable market factors, it falls under Level 3 of the fair value hierarchy.
In July 2024, Scranton entered into a loan agreement with funds controlled or managed by Oaktree (the "Loan Agreement") to refinance the loan that Scranton had initially obtained from banks in 2019. According to the terms of the Loan Agreement, this financing benefits from the following guarantees and security interest: (i) by a guarantee from BPC, (ii) a pledge of the shares of Haema and BPC, and (iii) pledges over the assets of BPC. Currently, Haema and its assets do not secure or guarantee this financing; however, based on the current terms of the Loan Agreement, it is expected that Haema will need to become a guarantor and grant security over its assets as collateral for the Loan Agreement.
In the event of a default under the Loan Agreement, the Selling Companies can, respectively and simultaneously, exercise the repurchase option for both companies within 90 days after receiving notification of the default. If the Selling Companies fail to exercise this option within that timeframe, they will lose their right to repurchase the shares of Haema and BPC. As of 31 December 2024, no defaults have been reported under the Loan Agreement.
In relation to the sale of the shares of BPC Plasma, Inc. and Haema, GmbH, a loan was signed by Scranton Enterprises BV. with the Group on 28 December 2018 for an initial amount of US Dollars 95,000 thousand (Euros 86,969 thousand). The remuneration is 2%+ EURIBOR and matures on 26 July 2027. In 2023 an additional amount of Euros 15 million was arranged under the same conditions as the initial loan. As of 31 December 2024, the recorded amount stands at Euros 131,864 thousand, including accrued and capitalized interest to date (Euros 115,209 thousand as of 31 December 2023) (see note 11) .
On November 22, 2017, the company Plasmavita Healthcare GmbH was incorporated in Germany. Currently, the Group is a shareholder of 50% of the shares and two individual partners, shareholders of the remaining 50% of the Company's shares. Through a management services agreement, one of them (the "Managing Partner") provides certain management services to the Company. The Company's incorporation agreement establishes a purchase option in favor of the Group that grants the irrevocable right (not the obligation) to the Group to acquire the remaining 50% stake in the Company from the two individual partners within a period of 6 months from the moment the Managing Partner ceases to provide the Company's management services. The fair value of the purchase option is not material.
On July 29, 2021, Grifols signed an agreement with the Egyptian company National Service Projects Organization ("NSPO") through which Grifols and NSPO has incorporated a new entity in Egypt for the construction and operation of 20 plasma collection centers, a fractionation plant, and a protein purification and dosing plant. Grifols and NSPO
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
hold 49% and 51% respectively in the new entity. The agreement includes a call option and a put option for both shareholders which allows them to acquire or sell their entire stake to the counterparty. These options can be exercised once the 10-year period from the creation of the company has elapsed. As the options are based on a variable number of shares and a variable amount, there is a derivative financial instrument that shall be measured at fair value through profit or loss. Given that the option price has been set at a value similar to the fair value of the new entity, the options do not have a significant value.
In September 2022, Grifols signed a collaboration agreement with Canadian Blood Services (CBS) to supply them with 2.4 million grains of Immunoglobulin exclusively through a network of Canadian plasma centers that should be fully developed and operational by July 2026. To achieve this goal, Grifols will need to collect 600.000 liters of Canadian plasma annually from Grifols-owned plasma centers in Canada. For this reason, Grifols has made the following commitments for the acquisition of plasma and self-built centers in Canada:
| Euros | |
|---|---|
| 2025 | 2026 |
| 12,433,448 | 61,265,816 |
As a consequence of the agreement to sell the 20% shareholding in Shanghai RAAS to Haier, both companies signed the following agreements:
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Details of legal proceedings in which the Company or Group companies are involved are as follows:
Cerus Corporation ("Cerus") and Laboratorios Grifols, S.A. ("Grifols") entered into a Manufacturing and Supply Agreement executed in 2016, pursuant to which Grifols was to manufacture and supply to Cerus processing and filters sets to be used by Cerus in its own product (the "Agreement"). As a result of Grifols' decision to discontinue the manufacturing, sale and support of its blood bag product business worldwide, Grifols was unable to comply with the Agreement. In December 2021, Cerus filed a notice of arbitration in the UK pursuant to the terms of the Agreement alleging wrongful termination of the Agreement by Grifols. Furthermore, in January 2022, Cerus filed injunctive measures with the Courts of Rubí (Barcelona) requiring the suspension of the closure of Grifols' blood bags production facility until the arbitration proceedings is finalized.
CURRENT PHASE: This January 2025, the parties have reached an agreement to put an end to the arbitration, by (a) executing, on 16 January 2025, a settlement agreement that discontinues the arbitration in exchange for the payment by Grifols to Cerus of the legal cost fixed at USD 1,091,731.31 and (b) executing, on 28 January 2025, a the deed of variation of the existing manufacturing and supply agreement which sets forth that the agreement is to continue in force and full effect until the new agreed-upon expiration date, namely, 30 October 2029. Consequently, all substantive issues have now been resolved, with only some minor procedural steps pending, such as, for example, paying the Tribunal's costs of around £36,000 which shall be assumed by Grifols.
On September 25, 2024, Grifols received notification that the Executive Committee of CNMV had initiated an administrative sanctioning procedure in connection with the conclusions reached by the CNMV on March 21, 2024. These conclusions were disclosed by the Company as Inside Information on the same date and subsequently supplemented. The proposed sanction against Grifols for the incidents mentioned in the conclusions and supplementary information does not exceed one Million Euros. On November 7, Grifols submitted allegations against the initiation of the administrative sanctioning procedure.
There a several recently filed wage and hour and related labor law class actions and/or California Private Attorneys General Act lawsuits that have been filed in California. These cases are in the very early stages and it is not yet known what the probability is that any of the cases can result in any potential relevant cash outflow for the Group. Based on past litigation and results, Grifols asserts that it is possible that one or more cases can reach to a material level in the future given the allegations of wage and hour violations, but at this time it is not probable to occur. In any case, Grifols will vigorously defend itself, and as part of its internal process, it will continue to asses, on a timely basis, any changes in facts and circumstances that may modify its risk evaluation. In the event that any of these contingencies becomes more probable, it will determine whether they could result in a material cash outflow.
Below is a breakdown of the financial instruments by nature, category and fair value. The Group does not provide details of the fair value of certain financial instruments as their carrying amount is very similar to their fair value because of its short term.
| Thousands of Euros | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 31/12/2024 | ||||||||||||
| Carrying amount | Fair Value | |||||||||||
| Financial assets at amortised costs |
Financial assets at FVTPL |
Financial assets at FV through OCI |
Hedges | Financial liabilities at amortised cost |
Other financial liabilities |
Total | Level 1 | Level 2 | Level 3 | Total | ||
| Non-current financial assets | — | 6,127 | 416,131 | — | — | — | 422,258 | 422,258 | — | — | 422,258 | |
| Derivative instruments | — | — | — | 7,246 | — | — | 7,246 | — | 7,246 | — | 7,246 | |
| Trade receivables | — | — | 531,674 | — | — | — | 531,674 | — | 531,674 | — | 531,674 | |
| Financial assets measured at fair value | — | 6,127 | 947,805 | 7,246 | — | — | 961,178 | |||||
| Non-current financial assets | 67,053 | — | — | — | — | — | 67,053 | |||||
| Other current financial assets | 237,510 | — | — | — | — | — | 237,510 | |||||
| Trade and other receivables | 251,334 | — | — | — | — | — | 251,334 | |||||
| Cash and cash equivalents | 979,780 | — | — | — | — | — | 979,780 | |||||
| Financial assets measured at amortized cost | 1,535,677 | — | — | — | — | — | 1,535,677 | |||||
| Derivatives instruments | — | (5,863) | — | — | — | — | (5,863) | — | (5,863) | — | (5,863) | |
| Financial liabilities measured at fair value | — | (5,863) | — | — | — | — | (5,863) | |||||
| Senior Unsecured & Secured Notes | — | — | — | — | (5,356,195) | — | (5,356,195) | (5,230,596) | — | — (5,230,596) | ||
| Promissory Notes | — | — | — | — | (73,177) | — | (73,177) | |||||
| Senior secured debt | — | — | — | — | (2,310,427) | — | (2,310,427) | — (2,360,113) | — (2,360,113) | |||
| Other bank loans | — | — | — | — | (345,905) | — | (345,905) | |||||
| Lease liabilities | — | — | — | — | (1,141,379) | — | (1,141,379) | |||||
| Other financial liabilities | — | — | — | — | (933,784) | — | (933,784) | |||||
| Trade and other payables | — | — | — | — | (1,062,483) | — | (1,062,483) | |||||
| Other current liabilities | — | — | — | — | — | (318,427) | (318,427) | |||||
| Financial liabilities measured at amortized cost | — | — | — | — | (11,223,350) | (318,427) (11,541,777) | ||||||
| 1,535,677 | 264 | 947,805 | 7,246 | (11,223,350) | (318,427) | (9,050,785) |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| 31/12/2023 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Carrying amount | Fair Value | ||||||||||
| Financial assets at amortised costs |
Financial assets at FVTPL |
Financial assets at FV through OCI |
Hedges | Financial liabilities at amortised cost |
Other financial liabilities |
Total | Level 1 | Level 2 | Level 3 | Total | |
| Non-current financial assets | — | 9,057 | 2,082 | — | — | — | 11,139 | 9,057 | — | 2,082 | 11,139 |
| Derivative instruments | — | — | — | 24,688 | — | — | 24,688 | — | 24,688 | — | 24,688 |
| Trade receivables | — | — | 213,231 | — | — | — | 213,231 | — | 213,231 | — | 213,231 |
| Financial assets measured at fair value (*) | — | 9,057 | 215,313 | 24,688 | — | — | 249,058 | ||||
| Non-current financial assets | 164,498 | — | — | — | — | — | 164,498 | ||||
| Other current financial assets | 116,588 | — | — | — | — | — | 116,588 | ||||
| Trade and other receivables | 506,815 | — | — | — | — | — | 506,815 | ||||
| Cash and cash equivalents | 529,577 | — | — | — | — | — | 529,577 | ||||
| Financial assets measured at amortized cost (*) | 1,317,478 | — | — | — | — | — | 1,317,478 | ||||
| Derivatives instruments | — | (10,144) | — | — | — | — | (10,144) | ||||
| Financial liabilities measured at fair value | — | (10,144) | — | — | — | — | (10,144) | — | (10,144) | — | (10,144) |
| Senior Unsecured & Secured Notes | — | — | — | — | (4,568,130) | — | (4,568,130) | ||||
| Promissory Notes | — | — | — | — | (114,188) | — | (114,188) | (4,364,798) | — | — (4,364,798) | |
| Senior secured debt | — | — | — | — | (3,179,333) | — | (3,179,333) | ||||
| Other bank loans | — | — | — | — | (1,144,459) | — | (1,144,459) | — (3,332,560) | — (3,332,560) | ||
| Lease liabilities | — | — | — | — | (1,111,329) | — | (1,111,329) | ||||
| Other financial liabilities | — | — | — | — | (929,636) | — | (929,636) | ||||
| Trade and other payables | — | — | — | — | (956,136) | — | (956,136) | ||||
| Other current liabilities | — | — | — | — | — | (283,366) | (283,366) | ||||
| Financial liabilities measured at amortized cost (*) | — | — | — | — | (12,003,211) | (283,366) (12,286,577) | |||||
| 1,317,478 | (1,087) | 215,313 | 24,688 (12,003,211) (283,366) (10,730,185) |
Thousands of Euros
(*) Restated figures (Note 2.d.)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
In order to determine the fair value of financial assets or liabilities, the Group uses the following hierarchy based on the relevance of the variables used:
This item provides information on the Group's exposure to risk associated with the use of financial instruments, the Group's objectives and procedures to measure and mitigate this risk, and the Group's capital management strategy.
The Group is exposed to the following risks
The Group's risk management policies are established to identify and analyze the risks faced by the Group, define appropriate risk limits and controls and to control risks and comply with limits. Risk management policies and procedures are reviewed regularly so that they reflect changes in market conditions and the Group's activities. The Group's management procedures and rules are designed to create a strict and constructive control environment in which all employees understand their duties and obligations.
The Group's Audit Committee supervises how management controls compliance with the Group's risk management procedures and policies and reviews whether the risk management policy is suitable considering the risks to which the Group is exposed. This committee is assisted by Internal Audit which acts as supervisor. Internal Audit performs regular and ad hoc reviews of the risk management controls and procedures and reports its findings to the Audit Committee.
Credit risk is the risk to which the Group is exposed in the event that a customer or counterparty to a financial instrument fails to discharge a contractual obligation, and mainly results from trade receivables and the Group's investments in financial assets.
The primary risk involves late payments from public entities, which is mitigated through the possibility of claiming interest as foreseen by Spanish legislation. No significant bad debt or late payment issues have been detected for sales to private entities.
The Group recognizes impairment based on its best estimate of the expected losses on trade and other receivables. The main impairment losses recognized are due to specific losses relating to individually identified risks. At year end, these impairment losses are immaterial.
For trade receivables the Group uses the simplified approach, estimating lifetime expected credit losses, while for all other financial assets the Group uses the general approach for calculating expected credit losses. In both cases, due to the customers' credit rating, as well as the internal classification systems currently in place for new customers and considering that collection periods are mostly around 30 days, there is no significant impact for the Group.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Grifols is exposed to credit risk from its operating activities, primarily through contractual assets, trade receivables, and other receivables, as well as from financing activities and the Group's financial assets.
The carrying amount of financial assets represents the maximum exposure to credit risk. At 31 December 2024 and 2023 maximum level of exposure to credit risk is as follows:
| Thousands of Euros | |||||
|---|---|---|---|---|---|
| Carrying amount | Reference | 31/12/2024 | 31/12/2023 | ||
| Non-current financial assets | Note 11 | 490,492 | 176,676 | ||
| Other current financial assets | Note 11 | 243,574 | 140,232 | ||
| Contractual assets | Note 14 | 36,036 | 47,751 | ||
| Trade receivables | Note 15 | 705,452 | 645,113 | ||
| Other receivables | Note 15 | 16,119 | 31,594 | ||
| Cash and cash equivalents | Note 16 | 979,780 | 529,577 | ||
| 2,471,453 | 1,570,943 |
Grifols regularly monitors its credit risk exposure with banks. The Group maintains a low credit risk profile by holding cash positions and derivative contracts with highly solvent financial institutions.
The Group has assessed the collectability of financial assets, and concluded that there is no significant risk of default.
The carrying amount of receivables and contractual assets by geographical area, at 31 December 2024 and 2023 is as follows:
| Thousands of Euros | ||||
|---|---|---|---|---|
| Carrying amount | 31/12/2024 | 31/12/2023 | ||
| Spain | 59,667 | 57,800 | ||
| EU countries | 116,367 | 79,951 | ||
| United States of America | 45,644 | 13,572 | ||
| Other European countries | 92,170 | 82,822 | ||
| Other regions | 427,640 | 458,719 | ||
| 741,488 | 692,864 | |||
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The following represent the carrying amount of the trade and other receivables and contractual assets categorized by due date as of 31 December 2024 is as follows:
| Thousands of Euros | ||||||
|---|---|---|---|---|---|---|
| Total gross carrying ECL Rate amount |
Provision | Total net third party trade receivables |
||||
| Not matured | 0.19 % | 621,498 | (626) | 620,872 | ||
| Past due 0-30 days | 0.19 % | 18,556 | (566) | 17,990 | ||
| Past due 31-60 days | 0.62 % | 24,577 | (150) | 24,427 | ||
| Past due 61-90 days | 2.03 % | 17,301 | (438) | 16,863 | ||
| Past due 91-180 days | 3.01 % | 36,366 | (1,065) | 35,301 | ||
| Past due 181-365 days | 8.52 % | 15,930 | (1,342) | 14,588 | ||
| More than one year | 100.00 % | 16,739 | (5,292) | 11,447 | ||
| — | — | — | ||||
| Customers with objective evidence of impairment |
11,388 | (11,388) | — | |||
| 762,355 | (20,867) | 741,488 |
An impairment matrix based on the length of time overdue was used to monitor receivables portfolios that do not show any specific indications of impairment in individual cases. For trade receivables related to customers from the Middle East which are overdue by more than one year, the flat-rate percentages from the impairment matrix were adjusted due to special default patterns.
The following represent the carrying amount of the trade and other receivables and contractual assets categorized by due date as of 31 December 2023 is as follows:
| Thousands of Euros | ||||||
|---|---|---|---|---|---|---|
| ECL Rate | Total gross carrying amount |
Provision | Total net third party trade receivables |
|||
| Not matured | 0.19 % | 524,699 | (560) | 524,136 | ||
| Past due 0-30 days | 0.19 % | 106,323 | (246) | 106,077 | ||
| Past due 31-60 days | 0.62 % | 19,428 | (119) | 19,309 | ||
| Past due 61-90 days | 2.03 % | 6,398 | (120) | 6,278 | ||
| Past due 91-180 days | 3.01 % | 9,283 | (279) | 9,004 | ||
| Past due 181-365 days | 8.52 % 6,749 |
(573) | 6,176 | |||
| More than one year | 100.00 % | 25,982 | (4,101) | 21,884 | ||
| Customers with objective evidence of impairment |
25,578 | (25,578) | — | |||
| 724,440 | (31,576) | 692,864 |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Movement in the bad debt provision was as follows:
| Thousands of Euros | |||||
|---|---|---|---|---|---|
| 31/12/2024 | 31/12/2023 | 31/12/2022 | |||
| Opening balance | 31,576 | 32,291 | 24,009 | ||
| Net charges for the year | 5,302 | 7,322 | 14,074 | ||
| Net cancellations for the year | (16,511) | (7,237) | (6,949) | ||
| Transfers | — | 47 | 53 | ||
| Translation differences | 500 | (847) | 1,104 | ||
| Closing balance | 20,867 | 31,576 | 32,291 |
Liquidity risk is the risk that the Group cannot meet its financial obligations as they fall due. The Group's approach to managing liquidity is to ensure where possible, that it always has sufficient liquidity to settle its obligations at the maturity date, both in normal conditions and in times of financial stress, to avoid incurring unacceptable losses or tarnishing the Group's reputation.
The Group manages liquidity risk on a prudent basis, based on availability of cash and sufficient committed unused long-term credit facilities, enabling the Group to implement its business plans and carry out operations using stable and secure sources of financing.
Liquidity at the end of the period stood at Euros 2.259.088 thousand (including undrawn committed credit lines), with the following details:
| Thousands of euros | ||||
|---|---|---|---|---|
| 31/12/2024 | 31/12/2023 | |||
| Current deposits | 5,100 | 6,506 | ||
| Cash in hand and at banks | 974,680 523,071 |
|||
| Total cash and cash equivalents | 979,780 | 529,577 | ||
| Undrawn committed credit lines | 1,279,308 | 615,328 | ||
| Total Liquidity | 2,259,088 | 1,144,905 |
The Credit Agreement establishes a limitation on the disposition of the "revolving line" that has not been exceeded as of 31 December 2023 and 2024.
The Group is able to provide sufficient liquidity to fund its current obligations based on cash flows from operations combined with cash balances and availability of unused credit lines, and it is committed to maintaining elevated and adequate levels of liquidity through internally generated cash flows. Additionally, currently the Group does not generate significant cash in any country that might have restrictions on the repatriation of funds.
As in previous years, the Group continues with its quarterly program for optimization of working capital, which is mainly based on contracts to sell receivables without recourse.
The main contractual obligations existing at the end of the fiscal year comprise mainly long-term financial debt obligations with capital repayments and interest payments (see note 21).
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Details of the contractual maturity dates of financial liabilities including committed interest calculated using interest rate forward curves are as follows:
| Thousands of Euros | ||||||||
|---|---|---|---|---|---|---|---|---|
| Carrying amount | Reference | Carrying amount at 31/12/2024 |
Contractual flows |
6 months or less |
6 - 12 months |
1-2 years | 2- 5 years | More than 5 years |
| Financial liabilities | ||||||||
| Bank loans | Note 21 | 2,656,332 | 3,162,629 | 361,583 | 110,212 | 176,452 | 2,514,382 | — |
| Other financial liabilities |
Note 21 | 933,785 | 1,488,690 | 185,618 | 6,871 | 115,842 | 414,309 | 766,050 |
| Bonds and other marketable securities |
Note 21 | 5,429,372 | 6,959,491 | 246,359 | 146,625 | 293,250 | 3,673,257 | 2,600,000 |
| Lease liabilities | Note 21 | 1,141,379 | 1,774,521 | 58,267 | 58,267 | 117,233 | 319,410 | 1,221,344 |
| Payable to suppliers | Note 22 | 852,305 | 852,305 | 847,854 | 4,451 | — | — | — |
| Other current liabilities | Note 23 | 41,277 | 41,277 | 24,276 | 16,997 | 4 | — | — |
| Financial derivatives | Note 30(d) | 5,863 | 5,863 | 5,863 | — | — | — | — |
| Total | 11,060,313 | 14,284,776 | 1,729,820 | 343,423 | 702,781 | 6,921,358 | 4,587,394 |
| Thousands of Euros | ||||||||
|---|---|---|---|---|---|---|---|---|
| Carrying amount | Reference | Carrying amount at 31/12/2023 |
Contractual flows |
6 months or less |
6 - 12 months |
1-2 years | 2- 5 years | More than 5 years |
| Financial liabilities | ||||||||
| Bank loans | Note 21 | 4,323,792 | 5,329,182 | 611,387 | 327,923 | 650,970 | 3,738,902 | — |
| Other financial liabilities |
Note 21 | 929,635 | 1,518,616 | 181,800 | 1,855 | 116,398 | 455,467 | 763,096 |
| Bonds and other marketable securities |
Note 21 | 4,682,319 | 5,304,861 | 187,543 | 73,571 | 1,978,190 | 3,065,557 | — |
| Lease liabilities | Note 21 | 1,111,328 | 1,562,912 | 53,551 | 53,551 | 126,133 | 326,253 | 1,003,424 |
| Payable to suppliers (*) | Note 22 | 822,955 | 813,114 | 811,943 | 1,171 | — | — | — |
| Other current liabilities (*) |
Note 23 | 17,398 | 16,651 | 16,496 | 155 | — | — | — |
| Financial derivatives | Note 30(d) | 10,144 | 10,144 | 10,133 | — | 11 | — | — |
| Total | 11,897,571 | 14,555,480 | 1,872,853 | 458,226 | 2,871,702 | 7,586,179 | 1,766,520 |
(*) Restated figures (Note 2.d.)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The Group operates internationally and is therefore exposed to currency risk when operating with foreign currencies, especially with regard to the US Dollar. Currency risk is associated with future commercial transactions, recognized assets and liabilities, and net investments in foreign operations.
The Group holds significant investments in foreign operations, the net assets of which are exposed to currency risk. The conversion risk affecting net assets of the Group's foreign operations in US Dollars is mitigated primarily through borrowings in this foreign currency.
The Group's main exposure to currency risk is with regard to the US Dollar, which is used in a significant percentage of transactions in foreign functional currencies.
The financing obtained in Euros represents 66% of the total debt of the Group and amounts to Euros 5,924 million at 31 December 2024 (62% and Euros 6,032 million at 31 December 2023). In this breakdown, 'Group debt' refers only to the nominal amount of the debt.
Until September 13, 2024, when the currency swap was canceled, part of the US Dollar debt of the Group was covered by a currency swap to hedge the exposure to the associated currency risk.
The Group applied the cost of hedging method. This method enabled the Group to exclude the currency basis spread from the designated hedging instrument and, subject to certain requirements, changes in their fair value attributable to this component were recognized in other comprehensive income.
Details of the Group's exposure to currency risk is as follows:
| Thousands of Euros 31/12/2024 |
|||
|---|---|---|---|
| 2,818 | 72,051 | ||
| 118,959 | 16,264 | ||
| 4,644,337 | — | ||
| 452,729 | 25,683 | ||
| (21,791) | (17,219) | ||
| (74,394) | (44,576) | ||
| (5,428,382) | (5,849) | ||
| (10,625) | — | ||
| (316,349) | 46,354 | ||
(*) Balances in Euros in subsidiaries with US Dollars functional currency
(**) Balances in US Dollars in subsidiaries with Euros functional currency
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| Thousands of Euros | ||||
|---|---|---|---|---|
| 31/12/2023 | ||||
| Euros (*) | US Dollars (**) | |||
| Trade receivables | 2,278 | 47,772 | ||
| Receivables from Group companies | 121,173 | 10,908 | ||
| Loans to Group companies | 4,818,407 | 41 | ||
| Cash and cash equivalents | 7,296 | 2,026 | ||
| Trade payables | (38,610) | (43,682) | ||
| Payables to Group companies | (119,801) | (30,643) | ||
| Loans from Group companies | (4,650,080) | — | ||
| Bank loans | (336,250) | — | ||
| Balance sheet exposure | (195,587) | (13,578) |
(*) Balances in Euros in subsidiaries with US Dollar functional currency
(**) Balances in US Dollar in subsidiaries with Euros functional currency
The most significant exchange rates applied at 2024 and 2023 year ends are as follows:
| Closing exchange rate | ||||
|---|---|---|---|---|
| Euros | 31/12/2024 | 31/12/2023 | ||
| US Dollars | 1.0390 | 1.1050 |
A sensitivity analysis for foreign exchange fluctuations is as follows:
Had the US Dollar strengthened by 10% against the Euro at 31 December 2024 equity would have increased by Euros 1,067,890 thousand (Euros 820,616 thousand at 31 December 2023) and profit due to foreign exchange differences would have decreased by Euros 27,000 thousand (Euros 20,638 thousand at 31 December 2023). This analysis assumes that all other variables are held constant, especially that interest rates remain constant.
A 10% weakening of the US Dollar against the Euro at 31 December 2024 and 31 December 2023 would have had the opposite effect for the amounts shown above, all other variables being held constant.
The Group uses hedge accounting to partially hedge the currency risk exposure (See note 30(d)).
The Group's interest rate risks arise from current and non-current borrowings. Borrowings at variable interest rates expose the Group to cash flow interest rate risks. Fixed-rate borrowings expose the Group to fair value interest rate risk.
The objective of the management of interest rate risk is to achieve a balance in the structure of the debt, keeping part of the external resources issued at a fixed rate and covering part of the variable rate debt through hedges.
A significant part of the financing obtained accrues interest at fixed rates, representing 71% of the total debt of the Group at 31 December 2024 (57% at 31 December 2023). It mainly includes corporate senior notes, European Investment Bank loans, as well as the agreement with GIC (Sovereign Fund of Singapore) (see note 21).
Variable-rate debt represents 29% of the total debt at 31 December 2024 (43% at 31 December 2023) and includes mainly the senior secured debt (see note 21(b)).
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
To date, the profile of interest on interest-bearing financial instruments is as follows:
| Thousands of Euros | ||||
|---|---|---|---|---|
| 31/12/2024 | 31/12/2023 | |||
| Fixed-interest financial instruments | 6,430,225 | 5,696,851 | ||
| Financial liabilities | 6,430,225 | 5,696,851 | ||
| Variable-interest financial instruments | 2,540,968 | 3,956,154 | ||
| Financial liabilities | 2,540,968 | 3,956,154 | ||
| 8,971,193 | 9,653,005 |
Had the interest rate been 100 basis points higher at 31 December 2024 the interest expense would have increased by Euros 29,954 thousand (Euros 34,114 thousand at 31 December 2023). As the Group does not have any hedging derivatives in place, the net effect on cash interest payments would have increased by the same amount .
In this breakdown, "financial liabilities" and "total debt" refer solely to the nominal amount of the debt.
Price risk affecting raw materials is mitigated by the vertical integration of the hemoderivatives business in a highly concentrated sector.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
At 31 December 2024 and 2023 the Group has recognized the following derivatives:
| Thousands of Euros | ||||||
|---|---|---|---|---|---|---|
| Financial derivatives | Currency | Notional at 31/12/2024 |
Notional at 31/12/2023 |
Value at 31/12/2024 |
Value at 31/12/2023 |
Maturity |
| Cross currency interest rate swap | US Dollar | — | 500,000 | — | 20,538 | 15/10/2024 |
| Cross currency interest rate swap | US Dollar | — | 205,000 | — | (140) | 15/10/2024 |
| Foreign exchange rate forward | Swiss Franc | 12,000 | 10,000 | — | 378 | 11/2/2025 |
| Foreign exchange rate forward | Canadian dollar | 240,202 | 32,667 | 3,654 | 450 | 11/02/2025 |
| Foreign exchange rate forward | Pound Sterling | 4,500 | — | 786 | — | 18/2/2025 |
| Foreign exchange rate forward | Japanese Yen | 1,200,000 | 700,000 | 438 | — | 18/2/2025 |
| Foreign exchange rate forward | Australian dollar | 9,000 | — | 278 | — | 28/1/2025 |
| Foreign exchange rate forward | Brazilian real | 70,000 | — | 288 | — | 18/2/2025 |
| Foreign exchange rate forward | Czech crown | 160,000 | 160,000 | — | 191 | 18/2/2025 |
| Foreign exchange rate forward | Mexican Peso | 50,000 | 90,000 | — | 193 | 18/2/2025 |
| Foreign exchange rate forward | Turkish lira | — | 87,835 | — | 44 | 31/1/2024 |
| Foreign exchange rate forward | US Dollar | — | 7,700 | — | 92 | 29/2/2024 |
| Foreign exchange rate forward | Euro | 240,246 | 40,000 | 315 | 1,412 | 30/1/2025 |
| Energy PPA | Euro / KwH | — | — | 1,486 | 1,529 | 31/12/2032 |
| Total derivative assets | 7,245 | 24,687 | ||||
| Cross currency interest rate swap | US Dollar | — | 205,000 | — | (7,712) | 13/9/2024 |
| Foreign exchange rate forward | Canadian dollar | 228,917 | 42,560 | (1,172) | (2,081) | 11/2/2025 |
| Foreign exchange rate forward | US Dollar | 39,385 | 2,000 | (764) | (2) | 26/2/2025 |
| Foreign exchange rate forward | Czech crown | 160,000 | 160,000 | (124) | (13) | 18/2/2025 |
| Foreign exchange rate forward | Pound Sterling | 4,500 | 8,500 | (353) | (122) | 18/2/2025 |
| Foreign exchange rate forward | Japanese Yen | 1,200,000 | 700,000 | (309) | (214) | 18/2/2025 |
| Foreign exchange rate forward | Euro | 240,246 | 40,000 | (2,615) | — | 30/1/2025 |
| Foreign exchange rate forward | Mexican Peso | 50,000 | 90,000 | (64) | — | 18/2/2025 |
| Foreign exchange rate forward | Australian dollar | 9,000 | — | (7) | — | 28/1/2025 |
| Foreign exchange rate forward | Swiss Franc | 12,000 | 10,000 | (455) | — | 11/2/2025 |
| Total derivative liabilities | (5,863) | (10,144) |
On 5 October 2021, the Group subscribed three cross currency interest-rate swaps with a notional amount of US Dollars 500 million to hedge part of the Euro equivalent value of the US Dollar unsecured notes issued in October 2021. It is a fixed-to-fixed USD/EUR cross currency swap with the following characteristics:
On 28 June 2022, the Group subscribed one cross currency interest-rate swap with a notional amount of US Dollars 205 million to hedge the remaining part of the Euro equivalent value of the US Dollar unsecured notes issued in October 2021. It is a fixed-to-fixed USD/EUR cross currency swap with the following characteristics:
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
On September 13, 2024, the cross-currency swap was terminated early. As of December 31, 2024, the Group recognized a net financial income of Euros 4,348 thousand under the heading 'Fair Value Change in Financial Instruments' in the Consolidated Statements of Profit and Loss (Euros 546 thousand as of December 31, 2023).
The derivative complies with the criteria required for hedge accounting. See further details in notes 4(i).
The Group has contracted several forward exchange rate hedges to partially cover the foreign currency value of intercompany loans. Since the Group has chosen not to apply hedge accounting, the gains or losses resulting from changes in the fair value of the derivative are recognized directly under the heading 'Fair Value Change in Financial Instruments' in the Consolidated Statements of Profit and Loss. As of December 31, 2024, the Group recognized a net financial income of Euros 15,534 thousand (Euros 2,005 thousand financial expense as of December 31, 2023).
At the beginning of 2023, the Company contracted a hedge on the variation of the price of electricity. This contract has served in its entirety to cover the purchase price of electricity against potential market price increases. The energy price hedging derivatives meet the requirements to apply hedge accounting, so the variations in the value of this financial instrument are recorded (by the net amount of taxes) in equity.
The movement in derivative financial instruments is as follows:
| Thousands of Euros | |||
|---|---|---|---|
| 31/12/2024 | 31/12/2023 | ||
| Opening balance | 14,543 | 34,923 | |
| Business combination | — | — | |
| Changes in fair value recognized in equity |
(1,690) | 1,914 | |
| Transfer to profit or loss | 27,267 | 5,775 | |
| Transfer to profit or loss - translation differences |
(208) | (23,037) | |
| Tax effect | (963) | (84) | |
| Collections / Payments | (37,568) | (4,948) | |
| Closing balance | 1,381 | 14,543 |
The directors' policy is to maintain a solid capital base in order to ensure investor, creditor and market confidence and sustain future business development. The board of directors defines and proposes the level of dividends paid to shareholders.
The capital structure is periodically reviewed through the preparation of strategic plans focused mainly on a sequential improvement of EBITDA (Earnings before interest, tax, amortization and depreciation), generation of operating cash and discipline in the allocation of capital; with the objective and commitment to reduce the leverage ratio.
In accordance with the senior secured debt contract, the Group is subject to compliance with some covenants. At 31 December 2024 and 2023, the Group complies with the covenants in the contract.
The credit rating of the Group is as follows: (Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| December 2024 | ||
|---|---|---|
| Moody's Investors | Corporate rating | B3 |
| Senior secured debt | B2 | |
| Senior Unsecured debt | Caa2 | |
| Perspective | Positive | |
| Standard & Poor's | Corporate rating | B+ |
| Senior secured debt | B+ | |
| Senior Unsecured debt | B | |
| Perspective | Stable | |
| Fitch Ratings | Corporate rating | B+ |
| Senior secured debt | BB | |
| Senior Unsecured debt | B | |
| Perspective | Stable |
The Parent held Class A and B treasury stock equivalent to 1.04% of its capital at 31 December 2024 (1.23% at 31 December 2023).
Details of balances with related parties at 31 December 2024 are a follows:
| Thousands of Euros | |||||
|---|---|---|---|---|---|
| Carrying amount | Reference | Associates | Key management personeel |
Other related parties |
|
| Receivables | 15 | 38,656 | — | — | |
| 3,085 | — | — | |||
| Other financial assets | 11 | 418 | — | — | |
| Loans | 11 | — | — | 214,119 | |
| Guarantee deposits | 11 | — | — | 943 | |
| Total debtors | 42,159 | — | 215,062 | ||
| Debts | — | (279) | (13,952) | ||
| Total creditors | — | (279) | (13,952) | ||
| — | — | — | |||
| Total | 42,159 | (279) | 201,110 |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Details of balances with related parties at 31 December 2023, restated to be comparative with details of balances with related parties for 2024, are as follows:
| Thousands of Euros | |||||
|---|---|---|---|---|---|
| Carrying amount | Reference | Associates | Other related parties |
Board of directors | |
| Receivables | 15 | 227,550 | 5,609 | — | |
| Other financial assets | 11 | 418 | — | — | |
| Loans | 11 | — | 216,426 | — | |
| Guarantee deposits | 11 | — | 934 | — | |
| Total debtors | 227,968 | 222,969 | — | ||
| Debts | — | (12,926) | (3,924) | ||
| Total creditors | — | (12,926) | (3,924) | ||
| Total | 227,968 | 210,043 | (3,924) |
The heading "Receivables" corresponding to associates includes outstanding balances from sales to associated companies, mainly corresponding in 2024 to Grifols Egypt Plasma Derivatives S.A.E. (Euros 205,537 thousand in 2023 and Euros 153,120 thousand in 2022 corresponding to Anhui Tonrol Pharmaceutical Co. (subsidiary of the Shanghai RAAS Blood Products, Co. Ltd. Group)). As of 31 December 2023, the balance of "Receivables" corresponding to other related parties corresponds entirely to an amount pending collection from Mr. Víctor Grifols Roura. This balance was settled in January 2024.
The heading "Loans" mainly includes a loan signed by Scranton Enterprises BV. with the Group on 28 December 2018 for an initial amount of US Dollars 95,000 thousand (Euros 86,969 thousand) (see note 11) related to the payment of the sale of the shares of BPC Plasma, Inc. and Haema, GmbH (see note 2). As of 31 December 2024 and 2023,the heading includes an additional amount of Euros 15 million arranged during 2023 under the same conditions as the initial loan (see note 31(b)). As of 31 December 2024, the recorded amount stands at Euros 131,864 thousand, including accrued and capitalized interest to date (Euros 115,209 thousand as of 31 December 2023).
Furthermore, it includes the cash-pooling financing agreement that BPC Plasma, Inc and Haema, GmbH have with Scranton Plasma, BV with maturity in 2027 (see note 11).
The heading of "debts" includes an amount of Euros 9,125 thousand at 31 December 2024 (Euros 17,732 thousand at 31 December 2023) corresponding to the balance of bearer promissory notes issued by the Group company Instituto Grifols, S.A. These promissory notes are due on 4 May 2025 and 2024, respectively, with a nominal value of Euros 3,000 each, and an annual nominal interest of 5% (4% in 2023)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Group transactions with related parties during 2024 are as follows:
| Thousands of Euros | |||||
|---|---|---|---|---|---|
| Associates | Key management personnel |
Other related parties |
Board of directors of the Company |
||
| Net sales | 269,733 | — | 117 | — | |
| Purchases | (2) | — | (235) | — | |
| Rendering of services | — | — | (4,848) | — | |
| Remuneration | — | (13,676) | — | (15,120) | |
| Payments for rights of use | — | — | (7,202) | — | |
| Finance income | — | — | 18,317 | — | |
| Dividends received/(paid) | 6,724 | — | (39,510) | — | |
| Loans | — | — | 44,937 | — | |
| Acquisition of assets | — | — | (35,000) | — | |
| 276,455 | (13,676) | (23,424) | (15,120) |
Group transactions with related parties during 2023 were as follows:
| Thousands of Euros | |||||
|---|---|---|---|---|---|
| Associates | Key management personnel |
Other related parties |
Board of directors of the Company |
||
| Net sales | 471,829 | — | 14 | — | |
| Purchases | (23) | — | (431) | — | |
| Rendering of services | (78) | — | (2,482) | — | |
| Remuneration | — | (23,698) | — | (12,163) | |
| Payments for rights of use | — | — | (7,234) | — | |
| Purchase of property, plant and equipment | — | — | — | — | |
| Finance income | — | — | 30,185 | — | |
| Dividends received/(paid) | 7,309 | — | (266,406) | — | |
| Loans | — | — | 44,956 | — | |
| 479,037 | (23,698) | (201,398) | (12,163) |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Group transactions with related parties during 2022 were as follows:
| Thousands of Euros | |||||
|---|---|---|---|---|---|
| Associates | Key management personnel |
Other related parties |
Board of directors of the Company |
||
| Net sales | 339,170 | — | — | — | |
| Purchases | (9) | — | — | — | |
| Rendering of services | (34) | — | (5,467) | — | |
| Remuneration | — | (13,891) | — | (5,316) | |
| Payments for rights of use | — | — | (6,382) | — | |
| Purchase of property, plant and equipment | — | — | 3,464 | — | |
| Finance income | — | — | 12,878 | — | |
| Dividends received/(paid) | 10,717 | — | — | — | |
| Loans | — | — | 80,098 | — | |
| 349,844 | (13,891) | 84,591 | (5,316) |
"Net sales" includes sales to associated companies mainly corresponding to Anhui Tonrol Pharmaceutical Co. (subsidiary of the Shanghai RAAS Blood Products, Co. Ltd. Group) (Euros 230,812 thousand in 2024, Euros 450,389 thousand in 2023 and Euros 319,669 thousand in 2022).
"Other service expenses" includes an amount of Euros 4,304 thousand corresponding to contributions to nonprofit entities in 2024 (Euros 2,174 thousand in 2023 and Euros 4,231 thousand in fiscal year 2022).
The dividends received correspond to the associated companies Shanghai RAAS Blood Products Co. Ltd., Bio Darou P.J.S. Co. and Access Biologicals LLC. Additionally, the dividends distributed correspond to BPC Plasma Inc. (see note 11).
"Acquisition of assets" includes the acquisition of Haema Plasma Kft for Euros 35,000 thousand that has been effected through the cancellation of a balance receivable that the Group had with Haema GmbH. This balance was transferred to Scranton Plasma B.V. and settled through the cash-pooling financing agreement held by these companies (se note 11).
Mr. Victor Grifols Roura, director representing shareholder's during 2023 and who resigned from his position as director in December 2023, received remuneration in 2023 of Euros 965 thousand.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The composition of the transactions with other related parties for in 2024, 2023 and 2022 is as follows:
| Thousands of Euros | |||||
|---|---|---|---|---|---|
| Related parties | Concept | Reference | 2024 | 2023 | 2022 |
| Scranton Enterprises, B.V. | Interest Credits | b) | 8,484 | 7,830 | 2,093 |
| Scranton Enterprises, B.V. | Finance Agreements: Credits | a) | — | 15,000 | — |
| Scranton Plasma B.V. | Interest Cash-pooling | b) | 9,833 | 22,355 | 10,785 |
| Scranton Plasma BV | Finance Agreements: Cash-pooling | a) | 44,937 | 29,956 | 80,098 |
| Scranton Plasma BV | Dividends paid/received | c) | (39,510) | (266,406) | — |
| Scranton Plasma BV | Shares acquisition | d) | (35,000) | — | — |
| Juve & Camps S.A. | Royalties | — | 14 | — | |
| Juve & Camps S.A. | Purchases | (83) | (8) | (169) | |
| Probitas Fundación Privada | Management and collaboration contracts | f) | (3,384) | (1,338) | (3,383) |
| Fundación Privada Victor Grifols Lucas | Management and collaboration contracts | f) | (465) | (407) | (450) |
| Club Joventut Badalona, S.A.D. | Rendering of services | (300) | (300) | (341) | |
| Centurion Real State, S.A.U | Payments for rights of use | e) | (7,141) | (7,147) | (6,300) |
| Centurion Real State, S.A.U | Improvement works | — | — | 3,464 | |
| Jose Antonio Grifols Lucas Foundation | Management and collaboration contracts | f) | (455) | (429) | (398) |
| Aurea Arrendamientos de Viviendas, S.A. | Payments for rights of use | (46) | (87) | (82) | |
| Qardio INC | Purchases | (152) | (431) | (726) | |
| More on Simplicity S.L. | Rendering of services | (41) | — | — | |
| Marca Grifols, S.L. | Royalties | g) | (187) | — | — |
| Medicover Försakrings AB Magyarorsz | Rendering of services | (16) | — | — | |
| Endo Operations Limited | Rendering of services | 117 | — | — | |
| Others | Payments for rights of use | (15) | — | — | |
| (23,424) | (201,398) | 84,591 |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
creditor under the Assigned Receivable against Haema GmbH, as debtor thereunder, has settled its debt position under the cash-pooling financing agreement in the amount of the Assigned Receivable (and hence, the amount outstanding under the cash-pooling arrangement between Haema GmbH, as creditor and Scranton Plasma B.V., as debtor, has been reduced in the amount of the Assigned Receivable)
The Group has not extended any advances or loans to the members of the board of directors or key management personnel nor has it assumed any guarantee commitments on their behalf. It has also not assumed any pension or life insurance obligations on behalf of former or current members of the board of directors or key management personnel. In addition, certain Company directors and key management personnel have termination benefit commitments (see note 29).
In July 2024, Scranton entered into a loan agreement with funds controlled or managed by Oaktree (the "Loan Agreement") to refinance the loan that Scranton had initially obtained from banks in 2019. According to the terms of the Loan Agreement, this financing benefits from the following guarantees and security interest: (i) by a guarantee from BPC, (ii) a pledge of the shares of Haema and BPC, and (iii) pledges over the assets of BPC. At the moment, Haema and its assets do not secure this financing; however, based on the current terms of the Loan Agreement, it is expected that that during the 2025 financial year, Haema will need to become a guarantor and grant security over its assets as collateral for the Loan Agreement (see note 29).
The Group has no advances or credits or obligations assumed on behalf of members of the Board of Directors or members of the key management staff as guarantees, nor pension and life insurance obligations in respect of former or current members of the Board of Directors or key members of management. In addition, certain managers and key management personnel have severance commitments (see note 29).
In July 2024, Scranton entered into a loan agreement with funds controlled or managed by Oaktree (the "Loan Agreement") to refinance the loan that Scranton had initially obtained from banks in 2019. According to the terms of the Loan Agreement, this financing benefits from the following guarantees and security interest: (i) by a guarantee from BPC Plasma, Inc, (ii) a pledge of the shares of Haema GmbH and BPC Plasma, Inc, and (iii) pledges over the assets of BPC Plasma, Inc. Currently, Haema GmbH and its assets do not secure or guarantee this financing; however, based on the current terms of the Loan Agreement, it is expected that Haema GmbH will need to become a guarantor and grant security over its assets as collateral for the Loan Agreement (see note 29).
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The Group carries out operations whose main purpose is to prevent, reduce or minimize the potential impact of its activities on the environment.
Grifols' environmental management is based on the concept of circular economy. Priority is given to the efficient use of material resources, water and energy, and waste generation is reduced, taking into account the different stages of the life cycle of products and services. This strategy integrates the transition towards a low-carbon economy which minimizes the impact on climate change
Since 2019, Grifols has updated its climate risk map based on its integrated management approach to climate change risks and opportunities, which the company uses to establish whether a material risk or opportunity could have a potential financial impact for the company.
This year, Grifols carried out an analysis of climate risks and opportunities taking into account the recommendations of the international scientific community, as well as the general criteria defined by reference frameworks such as the CSRD, analyzing a pessimistic stressed IPCC scenario for physical risks (SSP5-8.5) and another optimistic stressed IEA scenario for transition risks (NZS). In turn, and with a strategic approach, the analysis has also been carried out according to the recommendations of the TCFD and aligned with an average temperature increase of 2ºC (SSP2- RCP-4.5).
It has also been estimated the potential financial impacts arising from each of the material risks and opportunities. For a more detailed description of the methodology and results, please see the Consolidated Non Financial Information Statement and Sustainability Information.
During this process, 27 potential risks and opportunities arising from climate change were assessed, taking into account the company's entire value chain: suppliers (upstream water), its own operations and infrastructures, and the distribution and use of its products (downstream water). Following this analysis, 12 material risks and opportunities were identified for Grifols, 2 physical risks, 6 transition risks and 4 opportunities.
| Typology | Risks | Description | Financial impact | Risk management and mitigation |
|---|---|---|---|---|
| Physical (acute) | Increased frequency and intensity of heavy rainfall and floods |
An increase in the frequency and intensity of extreme rainfall and flooding, which could become more frequent in most regions due to global warming. Grifols has facilities in some of these regions. |
The potential impact of these events would consist of temporary production stoppages, or reduced plasma collection due to site closures. This would mean an increase in operational costs due to the transfer of production to plants not affected by this risk. And a reduction in income due to lower plasma collection at donation centers. |
In point 2.25 Adaptation to climate change in the Consolidated Non Financial Information Statement 2024, the measures that Grifols takes to mitigate this type of risk can be seen in greater detail. |
| Physical (chronic) Transition (political-legal) |
Decreased water availability in operations and supply chain Need to implement changes in water |
Grifols has facilities in areas where, under the simulated scenario, there could be difficulties in accessing water, or a change in water management regulations. |
These risks could translate into an increase in expenditure associated with obtaining water resources, a reduction in income due to a decrease in production capacity, and investments needed to optimize the water cycle in processes and facilities, from improving the efficiency of consumption to perfecting the purification process and, as far as |
Chapter 4. Water Resources in the Consolidated Non Financial Information Statement 2024 provides more detailed information on the measures Grifols takes to mitigate this type of risk. |
| management in operations |
possible, reuse of the resource. |
|||
| Transition (technological) |
Transition to low emission technologies |
Potential need to implement low or neutral emission technologies in the company's processes and facilities to comply with regulation and climate targets. |
To comply with regulations and climate targets, greater investment is required to reduce direct and indirect emissions, investments associated with the installation of air conditioning technologies, boilers and |
Throughout the environmental section of the Consolidated Non Financial Information Statement 2024, and in the Environmental Program, Grifols has defined several actions to reduce emissions and energy |
| Transition (Market/ reputational) |
Non-compliance with greenhouse gas emission reduction targets |
Risks of non-compliance with the scope 1 and 2 decarbonization targets set by Grifols. |
renewable energy generation aimed at reducing Grifols' emissions and increasing energy efficiency. And an |
efficiency. Exposure to this risk is expected to decrease as Grifols meets the targets set. |
| Transition (Market/ reputational) |
Non-compliance of suppliers with the climate targets set by the company |
Potential non compliance with emission reduction targets by Grifols' suppliers, which are necessary for the company to meet its own targets (scope 3 of the carbon footprint). |
increase in investment to offset the carbon footprint in the event of failure to meet decarbonization targets. |
|
| Transition (political-legal) |
Changing regulatory and reputational requirements for emissions reductions |
Climate change and energy efficiency regulations in some of the regions where Grifols is located are becoming increasingly stringent. |
||
| Transition (political-legal) |
Increased costs associated with the corporate carbon footprint |
Increased costs due to the increase in the price of neutralization credits. |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Four climate change-related opportunities have also been identified as material for Grifols. The first two are linked to resource efficiency, while the other two are related to efficient energy management.
The investment in environmental assets during the year ended 31 December 2024 is Euros 15,815 thousand (Euros 4,774 thousand in the year ended 31 December 2023 and Euros 8,372 thousand in the year ended 31 December 2022), mainly intended to optimize water consumption, improvements in wastewater treatment, eco-efficiency projects in the use of energy and the replacement of refrigerant gases with others with a lower environmental impact.
The expenses incurred by the Group for the protection and improvement of the environment in 2024 amounted to approximately Euros 28,340 thousand (Euros 28,034 thousand in 2023 and Euros 25,787 thousand in 2022).
With the procedures currently in place, the Group considers that environmental risks are adequately controlled
The Group's strategy is aligned with the objectives of the Paris Agreement and has been considered in the evaluation of the useful lives of assets and in the impairment analysis of non-financial assets. The Group does not anticipate impairment of assets before the established amortization periods.
The Group has not received any environmental subsidies during fiscal years 2024, 2023 and 2022.
The fees corresponding to Deloitte Auditores, S.L. or Companies of the same Network invoiced to the Group on 31 December 2024 and 2023 amount to:
| Thousands of Euros | ||||
|---|---|---|---|---|
| 2024 | 2023 | |||
| Audit services | 7,619 | 189 | ||
| Services required by applicable standards | 331 | — | ||
| 7,950 | 189 |
Amounts included in the table above, include the total amount of fees related to services incurred during 2024 and 2023, without considering the invoice date.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
Additionally, other audit firms have invoiced the Group for the following fees for professional services ended 31 December 2024 and 2023, fees for professional services, as detailed below:
| Thousands of Euros | ||||
|---|---|---|---|---|
| 2024 | 2023 | |||
| Audit services | 22 | 5,651 | ||
| Audit-related | — | 1,951 | ||
| Tax advisory fees | — | 4 | ||
| Other services | — | 127 | ||
| 22 | 7,733 |
In the 2024 fiscal year, audit services include limited reviews of interim financial statements, the audit of financial statements under PCAOB, as well as the performance of voluntary audits. Meanwhile, in the 2023 fiscal year, other accounting verification services include limited reviews of interim financial statements, the audit of financial statements under PCAOB, as well as the performance of audits under AICPA.
As scheduled under the in-force arrangements entered into by Grifols Bio North America LLC ("GBNA") and Immunotek GH LLC ("Immunotek") (the "Immunotek Collaboration Agreement"), with effects 2 January 2025, GBNA purchased a group of 8 plasma collection centres located in the US (the "Group 3 Centres") from Immunotek for a total net cash amount of approximately USD 78,888,000.
Furthermore, although pursuant to the Immunotek Collaboration Agreement the acquisition of the Group 4 Centres defined below was foreseen to take place in January 2026, in response to the strategic decision to optimise operational efficiency Immunotek and Grifols signed an amendment to the then in-force existing Immunotek Collaboration Agreement, whereby with effects as of 3 February 2025 GBNA purchased the last remaining 6 US plasma collection centres (the "Group 4 Centres") from Immunotek, for a purchase price of approximately US\$62,428,000, which payment obligation matures on 2 January 2026 (as foreseen in the original Immunotek Collaboration Agreement). As a result, Grifols has recognised a short-term liability in the 2025 financial year for the amount of the (deferred) purchase price of the Group 4 Centres.
Such deferral of the payment obligation has been documented in a promissory note between Biomat Holdings LLC, as issuer, and Immunotek, as Noteholder, for an amount of US\$69,343,084 (the "Promissory Note") (which includes management fees of approximately US\$ 7 million), maturing on 2 January 2026 and with no interest accrual. The Group 4 Centres act as collateral of the Promissory Note and (following the same guarantee provided by Grifols S.A. under the Immunotek Collaboration Agreement) the Promissory Note is guaranteed by Grifols, S.A.
Now therefore, and following the acquisition of the Group 3 Centres and the Group 4 Centres, Grifols has obtained control of the 14 centres on their acquisition date in 2025 (which had previously been considered within a joint operation) and now fully owns and will manage (from 1 May 2025), through its subsidiary Biomat Holdings LLC, all of the 28 US plasma collection centres developed by Immunotek under the Immunotek Collaboration Agreement. The collaboration with Immunotek has now been terminated (although Immunotek will continue to manage the Group 4 Centres until 30 April 2025 under a transitional services agreement), and GBNA is no longer a party in the joint venture company, Biotek America LLC.
Grifols has applied the requirements for a business combination carried out in stages. However, considering that (i) Grifols' effective participation in the joint operation is null and void and (ii) all of the assets and liabilities related to the joint operation are already recognized in the consolidated financial statements, the difference between the consideration paid and the fair value of the assets and liabilities, which does not differ from their carrying amount, has been recognized as provisional goodwill at the date of acquisition.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
The aggregate detail of the cost of the business combination and interim goodwill as of the acquisition date is shown below:
| Thousands of Euros | Thousands of US Dollar | |
|---|---|---|
| Consideration | 268,457 | 281,316 |
| Advance payment | (133,601) | (140,000) |
| Net consideration | 134,856 | 141,316 |
| Step-up of net assets adquired1 | — | — |
| Goodwill | 268,457 | 281,316 |
| Adjustments from acquisition 2 | (23,064) | (24,169) |
| Goodwill, net of adjustments | 245,393 | 257,147 |
1There is no step-up of net of assets since the fair value and the carrying amount do no differ significantly. Additionally, the net assets were previously recognized in the consolidated financial statements as part of the joint operation.
2The adjustments resulting from the acquisition correspond mainly to the elimination of the net balance payable that the silos maintained with Immunotek. The net amount represents the accumulated losses from the silos, which were allocated to Immunotek in accordance with the terms of the contract (see note 10).
The resulting goodwill has been allocated to the Biopharma segment and includes the donor database, licenses and workforce.
Finally, on 3 February 2025, Immunotek released three out of the five guarantees that Grifols Shared Services North America, Inc. (a subsidiary fully owned and managed by the Grifols Group) had granted to Immunotek in June 2023 for lease contracts related to certain Immunotek plasma collection centres not affected by the collaboration under Biotek America LLC. The remaining two guarantees, with an amount totalling approximately US\$20 million, are still in force and are expected to remain in force for as long as the lease agreements remain in force, and which balance is being reduced as and when the underlying lease term is reduced.
On February 21, further commitments from banks amounting to USD 74.5 million were signed, increasing the Multicurrency Revolving Credit Facility (RCF) to USD 1,353 million until November 2025, and from that date onwards, to USD 938 million until its maturity in May 2027. The upsize in the extended RCF tranche is expected to become effective on or around 27 February 2025.
Information on Group Companies, Associates and others for the years ended 31 December 2024, 2023 and 2022
| 31/12/2024 | 31/12/2023 | 31/12/2022 | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Registered | % shares | % shares | % shares | |||||||
| Name | Office | Acquisition / Incorporation date |
Activity | Statutory Activity | Direct | Indirect | Direct | Indirect | Direct | Indirect |
| Fully Consolidated Companies |
||||||||||
| Diagnostic Grifols, S.A. | Polígono Levante Calle Can Guasch, s/n 08150 Parets del Vallès (Barcelona) Spain |
1987 | Industrial | Development and manufacture of diagnostic equipment, instruments and reagents. |
— % 55.000 % | — % 66.790 % | — % 66.790 % | |||
| Instituto Grifols, S.A. | Polígono Levante Calle Can Guasch, s/n 08150 Parets del Vallès (Barcelona) Spain |
1987 | Industrial | Plasma fractioning and the manufacture of haemoderivative pharmaceutical products. |
99.998 % | 0.002 % 99.998 % | 0.002 % 99.998 % | 0.002 % | ||
| Laboratorios Grifols, S.A. | Polígono Levante Calle Can Guasch, s/n 08150 Parets del Vallès (Barcelona) Spain |
1989 | Industrial | Production of glass- and plastic-packaged parenteral solutions, parenteral and enteral nutrition products and blood extraction equipment and bags. |
100.000 % | — % 100.000 % | — % 100.000 % | — % | ||
| Biomat, S.A. | Polígono Levante Calle Can Guasch, s/n 08150 Parets del Vallès (Barcelona) Spain |
1991 | Industrial | Analysis and certification of the quality of plasma used by Instituto Grifols, S.A. It also provides transfusion centres with plasma virus inactivation services (I.P.T.H). |
99.900 % | 0.100 % 99.900 % | 0.100 % 99.900 % | 0.100 % | ||
| Grifols Engineering, S.A. | Polígono Levante Calle Can Guasch, s/n 08150 Parets del Vallès (Barcelona) Spain |
2000 | Industrial | Design and development of the Group's manufacturing installations and part of the equipment and machinery used at these premises. The company also renders engineering services to external companies. |
99.950 % | 0.050 % 99.950 % | 0.050 % 99.950 % | 0.050 % | ||
| Biomat USA, Inc. | 2410 Lillyvale Avenue Los Angeles (California) United States |
2002 | Industrial | Procuring human plasma. | — % 78.750 % | — % 77.500 % | — % 76.250 % | |||
| Grifols Biologicals, LLC. | 5555 Valley Boulevard Los Angeles (California) United States |
2003 | Industrial | Plasma fractioning and the production of haemoderivatives. |
— % 100.000 % | — % 100.000 % | — % 100.000 % | |||
| Grifols Australia Pty Ltd. | Unit 5/80 Fairbank Clayton South Victoria 3149 Australia |
2009 | Industrial | Distribution of pharmaceutical products and the development and manufacture of reagents for diagnostics. |
100.000 % | — % 100.000 % | — % 100.000 % | — % | ||
| Medion Grifols Diagnostic AG |
Bonnstrasse,9 3186 Dügingen Switzerland |
2009 | Industrial | Development and manufacturing activities in the area of biotechnology and diagnostics. |
— % 55.000 % | — % 66.790 % | — % 66.790 % |
| 31/12/2024 % shares |
31/12/2023 % shares |
31/12/2022 % shares |
||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Registered | ||||||||||
| Name | Office | Acquisition / Incorporation date |
Activity | Statutory Activity | Direct | Indirect | Direct | Indirect | Direct | Indirect |
| Fully Consolidated Companies |
||||||||||
| Grifols Therapeutics, LLC. |
4101 Research Commons (Principal Address), 79 T.W. Alexander Drive, Research Triangle Park, North Carolina 277709, United States |
2011 | Industrial | Plasma fractioning and the production of haemoderivatives. |
— % 100.000 % | — % 100.000 % | — % 100.000 % | |||
| Grifols Worldwide Operations Limited |
Grange Castle Business Park, Grange Castle , Clondalkin, Dublin 22, Ireland |
2012 | Industrial | Packaging, labelling, storage, distribution, manufacture and development of pharmaceutical products and rendering of financial services to Group companies. |
100.000 % | — % 100.000 % | — % 100.000 % | — % | ||
| Progenika Biopharma, S.A. |
Parque Tecnológico de Vizcaya, Edificio 504 48160 Derio (Vizcaya) Spain |
2013 | Industrial | Development, production and commercialisation of biotechnological solutions. |
99.990 % | 0.010 % 99.990 % | 0.010 % 99.990 % | 0.010 % | ||
| Grifols Diagnostics Solutions, Inc. |
4560 Horton Street 94608 Emeryville, California United States |
2013 | Industrial | Manufacture and sale of blood testing products | — % 55.000 % 11.790 % 55.000 % 11.790 % 55.000 % | |||||
| Grifols Worldwide Operations USA Inc. |
13111 Temple Avenue, City of Industry, California 91746-1510 United States |
2014 | Industrial | Manufacture, warehousing, and logistical support for biological products. |
— % 100.000 % | — % 100.000 % | — % 100.000 % | |||
| Grifols Asia Pacific Pte, Ltd |
501 Orchard Road nº20-01 238880 Wheelock Place, Singapore |
2003 | Commercial | Distribution and sale of medical and pharmaceutical products. |
100.000 % | — % 100.000 % | — % 100.000 % | — % | ||
| Grifols Movaco, S.A. | Polígono Levante Calle Can Guasch, s/n 08150 Parets del Vallès (Barcelona) Spain |
1987 | Commercial | Distribution and sale of reagents, chemical products and other pharmaceutical specialities, and of medical and surgical materials, equipment and instruments for use by laboratories and health centres. |
99.999% | 0.001% | 99.999% | 0.001% | 99.999% | 0.001% |
| Grifols Portugal Productos Farmacéuticos e Hospitalares, Lda. |
Rua de Sao Sebastiao,2 Zona Industrial Cabra Figa 2635-448 Rio de Mouro Portugal |
1988 | Commercial | Import, export and commercialisation of pharmaceutical and hospital equipment and products, particularly Grifols products. |
0.010 % 99.990 % | 0.010 % 99.990 % | 0.010 % 99.990 % |
| Registered | 31/12/2024 | 31/12/2023 | 31/12/2022 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| % shares | % shares | % shares | ||||||||||||
| Name | Office | Acquisition / Incorporation date |
Activity | Statutory Activity | Direct | Indirect | Direct | Indirect | Direct | Indirect | ||||
| Fully Consolidated Companies |
||||||||||||||
| Avda. Americo Vespucio, | ||||||||||||||
| Grifols Chile, S.A. | 2242 Comuna de Conchali Santiago de Chile Chile |
1990 | Commercial | Development of pharmaceutical businesses, which can involve the import, production, commercialisation and export of related products. |
99.000 % | 1.000 % 99.000 % | 1.000 % 99.000 % | 1.000 % | ||||||
| Grifols USA, LLC. | 2410 Lillyvale Avenue Los Angeles (California) United States |
1990 | Commercial | Distribution and marketing of company products. | — % 100.000 % | — % 100.000 % | — % 100.000 % | |||||||
| Grifols Argentina, S.A. | Bartolomé Mitre 3690/3790, CPB1605BUT Munro Partido de Vicente Lopez Argentina |
1991 | Commercial | Clinical and biological research. Preparation of reagents and therapeutic and diet products. Manufacture and commercialisation of other pharmaceutical specialities. |
95.010 % | 4.990 % 95.010 % | 4.990 % 95.010 % | 4.990 % | ||||||
| Grifols s.r.o. | Calle Zitna,2 Prague Czech Republic |
1992 | Commercial | Purchase, sale and distribution of chemical pharmaceutical products, including human plasma. |
100.000 % | — % 100.000 % | — % 100.000 % | — % | ||||||
| Grifols (Thailand) Ltd | 191 Silom Complex Building, 21st Follor, Silom Road, Silom, Bangrak 10500 Bangkok Thailand |
2003 | Commercial | Import, export and distribution of pharmaceutical products. |
— % 48.000 % | — % 48.000 % | — % 48.000 % | |||||||
| Grifols Malaysia Sdn Bhd | Level 18, The Gardens North Tower, Mid Valley City, Lingkaran Syed Putra 59200 Kuala Lumpur Malaysia |
2003 | Commercial | Distribution and sale of pharmaceutical products. | — % 100.000 % | — % 49.000 % | — % 49.000 % | |||||||
| Grifols International, S.A. | Polígono Levante Calle Can Guasch, s/n 08150 Parets del Vallès (Barcelona) Spain |
1997 | Commercial | Coordination of the marketing, sales and logistics for all the Group's subsidiaries operating in other countries. |
99.998 % | 0.002 % 99.998 % | 0.002 % 99.998 % | 0.002 % | ||||||
| Grifols Italia S.p.A | Via Carducci, 62d 56010 Ghezzano Pisa, Italy |
1997 | Commercial | Purchase, sale and distribution of chemical pharmaceutical products. |
100.000 % | — % 100.000 % | — % 100.000 % | — % |
| 31/12/2024 % shares |
31/12/2023 % shares |
31/12/2022 % shares |
||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Registered | ||||||||||
| Name | Office | Acquisition / Incorporation date |
Activity | Statutory Activity | Direct | Indirect | Direct | Indirect | Direct | Indirect |
| Fully Consolidated Companies |
||||||||||
| Grifols UK Ltd. | Gregory Rowcliffe & Milners, 1 Bedford Row, London WC1R 4BZ United Kingdom |
1997 | Commercial | Distribution and sale of therapeutic and other pharmaceutical products, especially haemoderivatives. |
100.000 % | — % 100.000 % | — % 100.000 % | — % | ||
| Grifols Brasil, Lda. | Rua Umuarama, 263 Condominio Portal da Serra Vila Perneta CEP 83.325-000 Pinhais Paraná, Brazil |
1998 | Commercial | Import and export, preparation, distribution and sale of pharmaceutical and chemical products for laboratory and hospital use, and medical-surgical equipment and instruments. |
100.000 % | — % 100.000 % | — % 100.000 % | — % | ||
| Grifols France, S.A.R.L. | Arteparc, Rue de la Belle du Canet, Bât. D, Route de la Côte d'Azur, 13590 Meyreuil France |
1999 | Commercial | Commercialisation of chemical and healthcare products. |
99.990 % | 0.010 % 99.990 % | 0.010 % 99.990 % | 0.010 % | ||
| Grifols Polska Sp.z.o.o. | Grzybowska 87 street00-844 Warsaw, Poland |
2003 | Commercial | Distribution and sale of pharmaceutical, cosmetic and other products. |
100.000 % | — % 100.000 % | — % 100.000 % | — % | ||
| Grifols México, S.A. de C.V. |
Calle Eugenio Cuzin, nº 909-913 Parque Industrial Belenes Norte 45150 Zapopán Jalisco, Mexico |
1993 | Commercial | Production, manufacture, adaptation, conditioning, sale and purchase, commissioning, representation and consignment of all kinds of pharmaceutical products and the acquisition of machinery, equipment, raw materials, tools, movable goods and property for the aforementioned purposes. |
100.000 % | — % 100.000 % | — % 100.000 % | — % | ||
| Grifols Nordic, AB | Sveavägen 166 11346 Stockholm Sweden |
2010 | Commercial | Research and development, production and marketing of pharmaceutical products, medical devices and any other asset deriving from the aforementioned activities. |
100.000 % | — % 100.000 % | — % 100.000 % | — % | ||
| Grifols Colombia, Ltda | Carrera 7 No. 71 52 Torre B piso 9 Bogotá. D.C. Colombia |
2010 | Commercial | Sale, commercialisation and distribution of medicines, pharmaceutical (including but not limited to haemoderivatives) and hospital products, medical devices, biomedical equipment, laboratory instruments and reagents for diagnosis and/or healthcare software. |
99.990 % | 0.010 % 99.990 % | 0.010 % 99.990 % | 0.010 % |
| 31/12/2024 | 31/12/2023 | 31/12/2022 | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Registered | % shares | % shares | % shares | |||||||
| Name | Office | Acquisition / Incorporation date |
Activity | Statutory Activity | Direct | Indirect | Direct | Indirect | Direct | Indirect |
| Fully Consolidated Companies |
||||||||||
| Grifols Deutschland GmbH |
Lyoner Strasse 15, D 60528 Frankfurt am Main Germany |
2011 | Commercial | Procurement of the official permits and necessary approval for the production, commercialisation and distribution of products deriving from blood plasma, as well as the import, export, distribution and sale of reagents and chemical and pharmaceutical products, especially for laboratories and health centres and surgical and medical equipment and instruments. |
100.000 % | — % 100.000 % | — % 100.000 % | — % | ||
| Grifols Canada, Ltd. | 5060 Spectrum Way, Suite 405 (Principal Address) Mississauga, Ontario L4W 5N5 Canada |
2011 | Commercial | Distribution and sale of biotechnological products. | 100.000 % | — % 100.000 % | — % 100.000 % | — % | ||
| Grifols Pharmaceutical Technology (Shanghai) Co., Ltd. |
Unit 901-902, Tower 2, No. 1539, West Nanjing Rd., Jing'an District, Shanghai 200040 China |
2013 | Commercial | Pharmaceutical consultancy services (except for diagnosis), technical and logistical consultancy services, business management and marketing consultancy services. |
100.000 % | — % 100.000 % | — % 100.000 % | — % | ||
| Grifols (H.K.), Limited | Units 1505-7 BerKshire House, 25 Westlands Road Hong Kong |
2014 | Commercial | Distribution and sale of diagnostic products. | — % 55.000 % | — % 66.790 % | — % 66.790 % | |||
| Grifols Japan K.K. | Hilton Plaza West Office Tower, 19th floor. 2-2, Umeda 2-chome, Kita-ku Osaka-shi Japan |
2014 | Commercial | Research, development, import and export and commercialisation of pharmaceutical products, devices and diagnostic instruments. |
100.000 % | — % 100.000 % | — % 100.000 % | — % | ||
| Grifols India Healthcare Private Ltd |
Regus Business Centre Pvt.Ltd.,Level15,Dev Corpora, Plot No.463,Nr. Khajana East.Exp.Highway,Thane (W), Mumbai - 400604, Maharashtra India |
2014 | Commercial | Distribution and sale of pharmaceutical products. | 99.984 % | 0.016 % 99.984 % | 0.016 % 99.984 % | 0.016 % |
| 31/12/2024 % shares |
31/12/2023 % shares |
31/12/2022 % shares |
||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Registered | ||||||||||
| Name | Office | Acquisition / Incorporation date |
Activity | Statutory Activity | Direct | Indirect | Direct | Indirect | Direct | Indirect |
| Fully Consolidated Companies |
||||||||||
| Grifols Diagnostics Equipment Taiwan Limited |
8F., No.367, Fuxing N. RD., Songshang Dist., Taipei City 10543, Taiwan |
2016 | Commercial | Distribution and sale of diagnostic products. | 100.000 % | — % 100.000 % | — % 100.000 % | — % | ||
| Grifols Viajes, S.A. | Can Guasch, 2 08150 Parets del Vallès Barcelona, Spain |
1995 | Services | Travel agency exclusively serving Group companies. | 99.900 % | 0.100 % 99.900 % | 0.100 % 99.900 % | 0.100 % | ||
| Squadron Reinsurance Designated Activity Company |
The Metropolitan Building, 3rd Fl. James Joyce Street, Dublin Ireland |
2003 | Services | Reinsurance of Group companies' insurance policies. | — % 100.000 % | — % 100.000 % | — % 100.000 % | |||
| Grifols Shared Services North America, Inc. |
2410 Lillivale Avenue 90032 Los Angeles, California United States |
2011 | Services | Support services for the collection, manufacture, sale and distribution of plasma derivatives and related products. |
100.000 % | — % 100.000 % | — % 100.000 % | — % | ||
| Gripdan Invest, S.L (merged with Grifols S.A.) |
Avenida Diagonal 477 Barcelona, Spain |
2015 | Services | Rental of industrial buildings | — % | — % | — % | — % 100.000 % | — % | |
| Araclon Biotech, S.L. | Paseo de Sagasta, 17 2º izqda. Zaragoza, Spain |
2012 | Research | Creation and commercialisation of a blood diagnosis kit for the detection of Alzheimer's and development of effective immunotherapy (vaccine) against this disease. |
— % 75.880 % | — % 75.880 % | — % 75.880 % | |||
| Grifols Innovation and New Technologies Limited |
Grange Castle Business Park, Grange Castle , Clondalkin, Dublin 22, Ireland |
2016 | Research | Biotechnology research and development | — % 100.000 % | — % 100.000 % | — % 100.000 % | |||
| Kiro Grifols S.L | Polígono Bainuetxe, 5, 2º planta, Aretxabaleta, Guipúzcoa Spain |
2014 | Research | Development of machines and equipment to automate and control key points of hospital processes, and hospital pharmacy processes. |
99.700 % | 0.300 % 99.700 % | 0.300 % 99.700 % | 0.300 % | ||
| Chiquito Acquisition Corp. (merged with Grifols Bio Supplis Inc.) |
2711 Centerville Road Suite 400, Wilmington, Delaware, New Castle County, United States |
2017 | Corporate | Engage in any lawful act or activity for which a corporation may be organized under the General Corporation Law of the State of Delaware, as amended from time to time (the "DGCL"). |
— % | — % | — % | — % | — % 100.000 % |
| 31/12/2024 | 31/12/2023 | 31/12/2022 | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Registered | % shares | % shares | % shares | |||||||
| Name | Office | Acquisition / Incorporation date |
Activity | Statutory Activity | Direct | Indirect | Direct | Indirect | Direct | Indirect |
| Fully Consolidated Companies |
||||||||||
| Aigües Minerals de Vilajuiga, S.A. |
Carrer Sant Sebastià, 2, 17493 Vilajuïga, Girona, Spain |
2017 | 2 0 Industrial 1 7 |
Collection and use of mineral-medicinal waters and obtaining of all necessary administrative concessions for the optimum and widest use of these. |
99.990 % | 0.010 % 99.990 % | 0.010 % 99.990 % | 0.010 % | ||
| Goetech LLC (D/B/A Medkeeper) |
7600 Grandview Avenue, Suite 210, Arvada, CO 8 0002, United States |
2018 | Industrial | Development and distribution of web and mobile based platforms for hospital pharmacies |
— % | — % | — % | — % | — % 100.000 % | |
| Grifols Bio Supplies Inc. (before Interstate Blood Bank, Inc.) |
5700 Pleasantville Road Memphis, Tennessee United States |
2016 | Industrial | Procurement of human plasma. | — % 100.000 % | — % 100.000 % | — % 100.000 % | |||
| Haema, GmbH (formerly Haema, AG) |
LandsteinerstraBe 1, 041 03 Leipzig - Germany |
2018 | Industrial | Procurement of human plasma. | — % | — % | — % | — % | — % | — % |
| BPC Plasma, Inc (formerly Biotest Pharma Corp) |
901 Yamato Rd., Suite 101, Boca Raton FL 33431 - United States |
2018 | Industrial | Procurement of human plasma. | — % | — % | — % | — % | — % | — % |
| Haema Plasma Kft. | Bajcsy-Zsilinszky út 12., 1051 Budapest (Hungría) |
2021 | Industrial | Procurement of human plasma. | — % 100.000 % | — % | — % | — % | — % | |
| Alkahest, Inc. | 3500 South DuPont Hwy, Dover, County of Kent United States |
2015 | Research | Development of novel plasma-based products for the treatment of cognitive decline in aging and disorders of the central nervous system (CNS). |
— % 100.000 % | — % 100.000 % | — % 100.000 % | |||
| Plasmavita Healthcare GmbH |
Colmarer Strasse 22, 60528 Frankfurt am Main - Germany |
2018 | Industrial | Procurement of human plasma. | — % 50.000 % | — % 50.000 % | — % 50.000 % | |||
| Plasmavita Healthcare II GmbH |
Garnisongasse 4/12, 1090 Vienna, Austria |
2019 | Industrial | Procurement of human plasma. | — % 50.000 % | — % 50.000 % | — % 50.000 % | |||
| Grifols Canada Therapeutics Inc. (formerly Green Cross Biotherapeutics; Inc) |
2911 Avenue Marie Curie, Arrondissement de Saint-Laurent, Quebec Canada |
2020 | Industrial | Conducting business in Pharmceuticals and Medicines Industry |
0.020 % 99.980 % | 0.020 % 99.980 % | 0.020 % 99.980 % | |||
| Grifols Laboratory Solutions, Inc |
Corporation Trust Center, 1209, Orange Street, Wilmington, New Castle Country, Delaware, 19801 United States |
2020 | Services | Engage in any lawful act or activity for which corporations may be organized under the General Corporation Law of Delaware |
— % 100.000 % | — % 100.000 % | — % 100.000 % |
| 31/12/2024 | 31/12/2023 | 31/12/2022 | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Registered | % shares | % shares | % shares | |||||||
| Name | Office | Acquisition / Incorporation date |
Activity | Statutory Activity | Direct | Indirect | Direct | Indirect | Direct | Indirect |
| Fully Consolidated Companies |
||||||||||
| Grifols Korea Co., Ltd. | 302 Teheran-ro, Gangnam-gu, Seoul (Yeoksam-dong) Korea |
2020 | Commercial | Import, export of diagnostic in vitro products and solutions. |
100.000 % | — % 100.000 % | — % 100.000 % | — % | ||
| Grifols Middle East & Africa LLC |
Office No. 534, 5th floor, NamaaBuilding No.155, Ramses Extension Street, Al Hay Al Sades, Nasr City, Cairo Egypt |
2021 | Services | Providing consultation (except for those stipulated in Article 27 of the Capital Market Law and its executive regulations) and carry out those commercial activities that are permitted by the law. |
99.990 % | 0.010 % 99.990 % | 0.010 % 99.990 % | 0.010 % | ||
| GigaGen Inc. | 407 Cabot Road South San Francisco, CA 94080, United States |
2017 | Industrial | Engage in any lawful act or activity for which corporations may be organized under General Corporation Law. |
— % 100.000 % | — % 100.000 % | — % 100.000 % | |||
| Grifols Pyrenees Research Center, S.L. |
C/ Prat de la Creu, 68-76, Planta 3ª, Edifici Administratiu del Comú d'Andorra la Vella Andorra |
2021 | Industrial | Constitution, development and management of operations of a research and development center in all areas of immnology, dedicated to find possible solutions for therapeutic applications. |
— % 100.000 % | — % 80.000 % | — % 80.000 % | |||
| Grifols Bio North America LLC |
251 Little Falls Drive, Wilmington, New Castle County, 19808, Delaware United States |
2021 | Industrial | Engage in any lawful business permitted by the Act or the laws of any jurisdiction in which the Company may do business. |
— % 100.000 % | — % 100.000 % | — % 100.000 % | |||
| Biomat Holdings LLC | 2410 Grifols Way, Los Angeles, California, 90032, United States. |
2023 | Services | Administration and financing services to Immunotek donor centers. |
— % 100.000 % | — % 100.000 % | — % | — % | ||
| Biomat Holdco, LLC. | 251 Little Falls Drive, Wilmington, New Castle County, Delaware, 19808 United States |
2021 | Services | Engage in any lawful act or activity for which corporations may be organized under General Corporation Law of Delaware. |
— % 100.000 % | — % 100.000 % | — % 100.000 % | |||
| Biomat Newco, Corp. | 251 Little Falls Drive, Wilmington, New Castle County, Delaware, 19808 United States |
2021 | Services | Engage in any lawful act or activity for which corporations may be organized under General Corporation Law of Delaware. |
— % 90.000 % | — % 88.600 % | — % 87.100 % |
| 31/12/2024 | 31/12/2023 | 31/12/2022 | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Registered | % shares | % shares | % shares | |||||||
| Name | Office | Acquisition / Incorporation date |
Activity | Statutory Activity | Direct | Indirect | Direct | Indirect | Direct | Indirect |
| Fully Consolidated Companies |
||||||||||
| Grifols Escrow Issuer, S.A. (merged with Grifols, S.A.) |
Parque Empresarial Can Sant Joan, Avda de la Generalitat, 152-156, Sant Cugat del Vallès, 08174, Barcelona Spain |
2021 | Services | Administration, management and control services for companies and businesses, as well as investment in property, as well as providing advisory services of any investee entities or group companies. |
— % | — % | — % | — % 100.000 % | — % | |
| Grifols Canada Plasma, Inc. (formerly Prometic Plasma Resources, Inc.) |
531 Boul. Des Prairies, Building 15 Laval, Quebec H7V 1B7 Canada |
2021 | Industrial | Procurement of human plasma. | — % 100.000 % | — % 100.000 % | — % 100.000 % | |||
| Grifols Canada Plasma – Ontario Inc. (formerly Canada Inc.) |
2911 av. Marie-Curie, Montreal, Quebec, H4S0B7, Canada |
2023 | Services | Administration, operating management and control services of plasma recollecting centers, directly or indirectly, through its affiliates. |
— % 100.000 % | — % 100.000 % | — % | — % | ||
| Access Biologicals, LLC (merged with Grifols Bio Supplies, Inc.) |
955, Park Center Drive, Vista, CA 92801, United States |
2017 | Industrial | Manufacture of biological products such as specific serum and plasma reagents that are used by biotechnological and biopharmaceutical companies for in-vitro diagnosis, cell culture and research and development in the field of diagnostics. |
— % | — % | — % | — % | — % 100.000 % | |
| Access Biologicals IC DISC, Inc. (merged with Grifols Bio Supplies, Inc.) |
995 Park Center Dr, Vista, CA 92081, United States |
2017 | Industrial | Manufacture of biological products, including specific sera and plasma-derived reagents, which are used by biotechnology and biopharmaceutical companies for in-vitro diagnostics, cell culture, and research and development in the diagnostic field. |
— % | — % | — % | — % | — % 100.000 % | |
| Access Cell Culture, LLC. (merged with Grifols Bio Supplies, Inc.) |
995 Park Center Dr, Vista, CA 92081, United States |
2017 | Industrial | Manufacture of biological products, including specific sera and plasma-derived reagents, which are used by biotechnology and biopharmaceutical companies for in-vitro diagnostics, cell culture, and research and development in the diagnostic field. |
— % | — % | — % | — % | — % 100.000 % | |
| Access Plasma, LLC. (merged with Grifols Bio Supplies, Inc.) |
995 Park Center Dr, Vista, CA 92081, United States |
2017 | Industrial | Manufacture of biological products, including specific sera and plasma-derived reagents, which are used by biotechnology and biopharmaceutical companies for in-vitro diagnostics, cell culture, and research and development in the diagnostic field. |
— % | — % | — % | — % | — % 100.000 % |
| 31/12/2024 | 31/12/2023 | 31/12/2022 | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Registered | % shares | % shares | % shares | |||||||
| Name | Office | Acquisition / Incorporation date |
Activity | Statutory Activity | Direct | Indirect | Direct | Indirect | Direct | Indirect |
| Fully Consolidated Companies |
||||||||||
| Albimmune, S.L. | Parque Empresarial Can Sant Joan, Avda de la Generalitat, 152-156, Sant Cugat del Vallès, 08174, Barcelona España |
2022 | Research | The purpose of the company is the research, development and exploitation of a project on the application of the use of albumin as a medicine |
— % 51.000 % | — % 51.000 % | — % 51.000 % | |||
| Biotest, AG | Landsteinerstr. 5, D-63303 Dreieich, Germany |
2022 | Industrial | Development, manufacture and distribution of biological, chemical, pharmaceutical, human and veterinary medical, cosmetic and dietary products as well as containers, devices, machines and accessories for medical, pharmaceutical and analytical purposes, as well as research in these fields. Furthermore the activity (especially research development, production and distribution) in the field of plant protection and plant breeding, the field of testing and purification of soil, water and air and in the field of products, materials and techniques used in space. |
24.700 % 45.480 % 24.700 % 45.480 % 24.700 % 45.480 % | |||||
| Biotest Austria, GmbH | Einsiedlergasse 58, A-1050, Vienna, Austria |
2022 | Industrial | Distribution of pharmaceutical products. | — % 70.180 % | — % 70.180 % | — % 70.180 % | |||
| Biotest Italia, S.R.L. (merged with Grifols Italia S.p.A) |
Via Leonardo da Vinci 43, I-20090 Trezzano sul Naviglio MI, Italy |
2022 | Industrial | Distribution of pharmaceutical products. | — % | — % 100.000 % | — % | — % 70.180 % | ||
| Biotest (UK) Ltd. (merged with Grifols UK, Ltd.) |
17 High Street, B31 2UQ Longbridge Birmingham, United Kingdom |
2022 | Industrial | Distribution of pharmaceutical products. | — % 100.000 % | — % 100.000 % | — % 70.180 % | |||
| Biotest (Schweiz) AG | Schützenstrasse 17, CH-5102 Rupperswil, Switzerland |
2022 | Industrial | Distribution of pharmaceutical products. | — % 70.180 % | — % 70.180 % | — % 70.180 % | |||
| Biotest Hungaria Kft | Torbágy utca 15/ A, Törökbálint 2045, Hungary |
2022 | Industrial | Procurement of human plasma. | — % 70.180 % | — % 70.180 % | — % 70.180 % | |||
| Biotest Farmacêutica LTDA (merged with Grifols Brasil Ltda.) |
Rua José Ramos Guimarães, 49 A Centro, 12955-000, Bom Jesus dos Perdões – SP, Brasil |
2022 | Industrial | Distribution of pharmaceutical products. | — % | — % 100.000 % | — % | — % 70.180 % |
| 31/12/2024 | 31/12/2023 | 31/12/2022 | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Registered | % shares | % shares | % shares | |||||||
| Name | Office | Acquisition / Incorporation date |
Activity | Statutory Activity | Direct | Indirect | Direct | Indirect | Direct | Indirect |
| Fully Consolidated Companies |
||||||||||
| Biotest Hellas M.E.P.E. | 45 Michalakopoulou Str., 11528 Athens, Greece |
2022 | Research | Research and development of solutions in the Biopharma area. |
— % 70.180 % | — % 70.180 % | — % 70.180 % | |||
| Biotest France SAS (merged with Grifols France S.A.R.L.) |
45/47 rue d'Hauteville, 75010 Paris, France |
2022 | Services | The purpose of the company is to act as an agent and support the group companies. |
— % | — % 100.000 % | — % | — % 70.180 % | ||
| Biotest Pharmaceuticals Ilaç Pazarlama Anonim Sirketi |
Nishstanbul, Cobançesme Mahallesi, 34197 Bahçeliever, Istanbul, Turkey |
2022 | Research | Research and development of solutions in the Biopharma area. |
— % 70.180 % | — % 70.180 % | — % 70.180 % | |||
| Biotest Medical, S.L.U. (merged with Grifols Movaco, S.A.) |
C/ Frederic Mompou, nº 5, 6º 3ª A, 08960 Sant Just Desvern, Barcelona, Spain |
2022 | Industrial | Distribution of pharmaceutical products. | — % | — % 100.000 % | — % | — % 70.180 % | ||
| Biotest Pharma, GmbH | Landsteinerstr. 5, D-63303 Dreieich, Germany |
2022 | Industrial | Carry out the development and production activities in the Biopharma area. |
— % 70.180 % | — % 70.180 % | — % 70.180 % | |||
| Biotest Lux S.à.r.l. | 17, Boulevard F.W. Raiffeisen L-2411 Luxembourg |
2023 | Services | Providing financing and centralisation of services for Biotest companies. |
— % 70.180 % | — % 70.180 % | — % | — % | ||
| BioDarou PLC | Sarparast St., Italia St. Felestin Ave, 1416653163 Tehran, Iran |
2022 | Industrial | Procurement of human plasma. | #REF! | #REF! | #REF! | #REF! | #REF! | #REF! |
| Biotest Grundstücksverwaltungs GmbH |
Landsteinerstr. 5, D-63303 Dreieich, Germany |
2022 | Services | Management of own assets. | — % 70.180 % | — % 70.180 % | — % 70.180 % | |||
| Plasma Service Europe GmbH |
Landsteinerstr. 5, D-63303 Dreieich, Germany |
2022 | Industrial | Procurement of human plasma. | — % 70.180 % | — % 70.180 % | — % 70.180 % | |||
| Cara Plasma s.r.o. | Jungmannova 745/24 - Nové Město, 110 00 Praha 1 , Czech Republic |
2022 | Industrial | Procurement of human plasma. | — % 70.180 % | — % 70.180 % | — % 70.180 % | |||
| Plazmaszolgálat Kft | Torbágy utca 15/ A, Törökbálint 2045, Hungary |
2022 | Industrial | Procurement of human plasma. | — % 70.180 % | — % 70.180 % | — % 70.180 % |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| 31/12/2024 % shares |
31/12/2023 % shares |
31/12/2022 % shares |
||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Registered | ||||||||||
| Name | Office | Acquisition / Incorporation date |
Activity | Statutory Activity | Direct | Indirect | Direct | Indirect | Direct | Indirect |
| Fully Consolidated Companies |
||||||||||
| Grifols Biotest Holdings GmbH |
Colmarer Str. 22, 60528 Frankfurt am Main, Germany |
2022 | Services | Management of own assets as well as the acquisition, sale, holding and management of shares in other companies in Germany and abroad in the company's own name and on its own account (not third parties), in particular in Biotest AG with registered offices in Dreiech. |
100.000 % | — % 100.000 % | — % 100.000 % | — % | ||
| AlbaJuna Therapeutics, S.L |
Hospital Germans Trias i Pujol, carretera de Canyet, s/n, Badalona, Spain |
2016 | Research | Development and manufacture of therapeutic antibodies against HIV. |
— % 100.000 % | — % 100.000 % | — % 49.000 % | |||
| This appendix is part of note 2 from the consolidated |
annual accounts.
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| 31/12/2024 | 31/12/2023 | 31/12/2022 | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Acquisition / | % shares | % shares | % shares | |||||||
| Name | Registered Office | Incorporation date |
Activity | Statutory Activity | Direct | Indirect | Direct | Indirect | Direct | Indirect |
| Equity-accounted investees and others | ||||||||||
| Mecwins, S.L. (no longer associated) |
Avenida Fernandos Casas Novoa, 37 Santiago de Compostela, Spain |
2013 | Research | Research and production of nanotechnological, biotechnological and chemical solutions. |
— % | — % | — % 24.590 % | — % 24.590 % | ||
| Albajuna Therapeutics, S.L (becomes part of the group) |
Hospital Germans Trias i Pujol, carretera de Canyet, s/n, Badalona Spain |
2016 | Research | Development and manufacture of therapeutic antibodies against HIV. |
— % | — % | — % | — % | — % 49.000 % | |
| Medcom Advance, S.A (dissolved) |
Av. Roma, 35 Entresuelo 1, 08018 Barcelona; Spain |
2019 | Research | Research and development of nanotechnological solutions. |
— % | — % | — % 45.000 % | — % 45.000 % | ||
| Shanghai RAAS Blood Products Co. Ltd. (no longer associated) |
2009 Wangyuan Road, Fengxian District, Shanghai |
2020 | Industrial | Introducing advanced and applicable technologies, instruments and scientific management systems for manufacturing and diagnosis of blood products, in order to raise the production capacity and enhance quality standards of blood products to the international level. |
— % | — % 26.200 % | — % 26.580 % | — % | ||
| Grifols Egypt for Plasma Derivatives (S.A.E.) |
Tolip El Narges Hotel, Teseen Streett, Fifth Settlement, Cairo Egypt |
2021 | Industrial | Establish and operate a plasma fractionation plant, regardless of whether the plasma is collected locally or imported, as well as its filling and packaging. |
49.000 % | — % 49.000 % | — % 49.000 % | — % | ||
| Biotek America LLC ("ITK JV") |
1430 East Southlake Blvd Suite 200 Southlake TX 76092 Estados Unidos |
2021 | Industrial | Build and manage until the opening of donor plasma centers in the United States. |
— % 75.000 % | — % 75.000 % | — % 75.000 % | |||
| BioDarou PLC | Sarparast St., Italia St. Felestin Ave, 1416653163 Tehran, Iran |
2022 | Industrial | Procurement of human plasma. | 0 | 0.34388 | 0 | 0.34388 | 0 | 0.34388 |
This appendix is part of note 2 from the consolidated annual accounts.
(expressed in thousands of Euros)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| Biopharma | Diagnostic | Bio Supplies | Others | Intersegments | Consolidated | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023(*) | 2022(*) | 2024 | 2023(*) | 2022(*) | 2024 | 2023(*) | 2022(*) | 2024 | 2023(*) | 2022(*) | 2024 | 2023(*) | 2022(*) | 2024 | 2023(*) | 2022(*) | ||
| Revenues from external customers | 6,142,588 5,558,301 5,005,382 | 644,898 | 670,269 | 671,292 | 215,664 | 159,957 | 146,076 | 209,232 | 203,450 | 250,165 | — | — | (8,948) | 7,212,382 6,591,977 6,063,967 | |||||
| Total operating income | 6,142,588 5,558,301 5,005,382 | 644,898 | 670,269 | 671,292 | 215,664 | 159,957 | 146,076 | 209,232 | 203,450 | 250,165 | — | — | (8,948) | 7,212,382 6,591,977 6,063,967 | |||||
| Profit/(Loss) for the segment | 1,271,194 | 886,978 | 768,095 | 108,829 | 111,694 | 129,968 | 47,793 | 43,563 | 114,397 | 39,435 | 6,632 | (46,809) | — | 6,979 | 35,419 | 1,467,251 1,055,846 1,001,070 | |||
| Unallocated expenses | (275,236) (273,529) (218,634) | ||||||||||||||||||
| Operating profit/(loss) | 1,192,015 | 782,317 | 782,436 | ||||||||||||||||
| Finance result | (748,019) (574,374) (442,941) | ||||||||||||||||||
| Share of profit/(loss) of equity | |||||||||||||||||||
| accounted investee | — | — | — | — | — | — | — | — | — | — | (922) | (1,482) | — | — | — | — | (922) | (1,482) | |
| Income tax expense | (231,190) | (43,349) | (90,111) | ||||||||||||||||
| Profit for the year after tax | 212,806 | 163,672 | 247,902 | ||||||||||||||||
| Segment assets | 14,232,889 13,419,636 13,464,608 | 3,754,840 3,528,861 3,681,632 | 348,789 | 380,012 | 341,876 | 889,606 1,840,949 | 766,139 | — | — | (6,997) 19,226,124 19,169,458 18,247,258 | |||||||||
| Equity-accounted investments | 68,996 | 57,529 | 41,162 | — | — | — | — | — | — | — | 364,234 1,456,797 | — | — | — | 68,996 | 421,763 1,497,959 | |||
| Unallocated assets | — | — | — | — | — | — | — | — | — | — | — | — | — | — | — | 2,110,121 1,400,882 1,484,367 | |||
| Total assets | 21,405,241 20,992,103 21,229,584 | ||||||||||||||||||
| Segment liabilities | 2,323,789 2,459,786 2,494,213 | 522,822 | 466,953 | 425,693 | 81,813 | 79,678 | 43,264 | 514,414 | 97,840 | 222,565 | — | — | — | 3,442,838 3,104,257 3,185,735 | |||||
| Unallocated liabilities | — | — | — | — | — | — | — | — | — | — | — | — | — | — | — | 9,355,378 10,374,151 10,067,720 | |||
| Total liabilities | 12,798,216 13,478,408 13,253,455 | ||||||||||||||||||
| Other information: | |||||||||||||||||||
| Allocated amortisation and depreciation | 327,743 | 333,103 | 297,272 | 64,522 | 65,817 | 64,682 | 9,305 | 9,280 | 5,759 | 15,696 | 16,162 | 20,367 | — | — | — | 417,266 | 424,362 | 388,080 | |
| Unallocated amortisation and depreciation | — | — | — | — | — | — | — | — | — | — | — | — | — | — | — | 20,630 | 22,060 | 22,900 | |
| Allocated expenses that do not require cash payments |
(5,143) | 30,198 | (71,964) | 4,613 | 6,995 | 13,639 | 105 | 136 | 120 | (8,208) | (789) | (206) | — | — | — | (8,633) | 36,540 | (58,411) | |
| Unallocated expenses that do not require cash payments |
— | — | — | — | — | — | — | — | — | — | — | — | — | — | — | (4,310) | 548 | (10,770) | |
| Allocated additions for the year of property, plant & equipment, intangible assets and rights of use |
373,380 | 359,442 | 507,457 | 54,575 | 29,107 | 49,890 | 2,128 | 9,066 | 98 | 7,619 | 3,884 | 30,192 | — | — | — | 437,702 | 401,499 | 587,637 | |
| Unallocated additions for the year of property, plant & equipment, intangible assets and rights of use |
— | — | — | — | — | — | — | — | — | — | — | — | — | — | — | 40,488 | 48,618 | 59,866 |
(*) Restated figures (Note 2.d)
This appendix forms an integral part of note 5 to the consolidated annual accounts.
(expressed in thousands of Euros)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| Spain | Rest of European Union | USA + Canada | Rest of World | Consolidated | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2,024 | 2023(*) | 2022(*) | 2,024 | 2023(*) | 2022(*) | 2,024 | 2023(*) | 2022(*) | 2,024 | 2023(*) | 2022(*) | 2,024 | 2023(*) | 2022(*) | |
| Net Revenue | 423,080 | 362,877 | 320,631 — 1,118,258 | 893,050 | 711,579 — 4,087,030 | 3,898,961 | 3,855,607 — 1,584,014 | 1,437,089 | 1,176,150 — 7,212,382 | 6,591,977 | 6,063,967 | ||||
| Assets by geographical area | 1,635,463 | 1,190,606 | 1,156,068 — 7,584,295 | 7,055,181 | 6,600,264 —11,789,971 10,966,924 11,713,893 — 395,512 | 1,779,392 | 1,759,359 —21,405,241 20,992,103 21,229,584 | ||||||||
| Other information: | |||||||||||||||
| Additions for the year of property, plant & | |||||||||||||||
| equipment, intangible assets and rights of use | 56,796 | 53,216 | 60,503 | 155,534 | 170,763 | 107,030 | 255,575 | 214,227 | 467,819 — | 10,285 | 11,911 | 12,151 | 478,190 | 450,117 | 647,503 |
(*) Restated figures (Note 2.d)
This appendix forms an integral part of note 5 to the consolidated annual accounts.
(expressed in thousands of Euros)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| Balance at 31/12/2023 |
Additions | Transfers | Disposals | Translation differences |
Balance at 31/12/2024 |
|
|---|---|---|---|---|---|---|
| Development costs | 1,853,483 | 102,092 | — | (2,472) | 49,866 | 2,002,969 |
| Concessions, patents, licenses brands & similar | 284,736 | 1,288 | 1,852 | (814) | 15,911 | 302,973 |
| Computer software | 359,837 | 25,915 | 4,883 | (1,755) | 12,432 | 401,312 |
| Currently marketed products | 1,389,248 | — | — | — | 74,095 | 1,463,343 |
| Other intangible assets | 117,172 | 9,534 | (1,521) | (3,012) | 4,953 | 127,126 |
| Total cost of intangible assets | 4,004,476 | 138,829 | 5,214 | (8,053) | 157,257 | 4,297,723 |
| Accum. amort. of development costs | (228,832) | (32,582) | — | 2,472 | (7,449) | (266,391) |
| Accum. amort of concessions, patents, licences, br. | (91,496) | (16,154) | — | 815 | (4,529) | (111,364) |
| Accum. amort. of cumputer software | (251,438) | (34,455) | — | 467 | (8,713) | (294,139) |
| Accum. amort. of currently marketed products | (499,347) | (49,262) | — | — | (31,454) | (580,063) |
| Accum. amort. of other intangible assets | (100,108) | (1,225) | — | — | (5,450) | (106,783) |
| Total accum. amort intangible assets | (1,171,221) | (133,678) | — | 3,754 | (57,595) | (1,358,740) |
| Impairment of other intangible assets | (1,059) | (10,113) | (1,794) | 140 | (25) | (12,851) |
| Carrying amount of intangible assets | 2,832,196 | (4,962) | 3,420 | (4,159) | 99,637 | 2,926,132 |
This appendix forms an integral part of Note 7 to the consolidated annual accounts.
(expressed in thousands of Euros)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| Balance at 31/12/2022 |
Additions | Transfers | Disposals | Translation differences |
Balance at 31/12/2023 |
|
|---|---|---|---|---|---|---|
| Development costs | 1,822,085 | 58,573 | — | — | (27,175) | 1,853,483 |
| Concessions, patents, licenses brands & similar | 292,158 | 2,747 | (344) | (1,478) | (8,347) | 284,736 |
| Computer software | 340,991 | 22,174 | 3,684 | (117) | (6,895) | 359,837 |
| Currently marketed products | 1,431,174 | — | — | — | (41,926) | 1,389,248 |
| Other intangible assets | 117,485 | 2,388 | (157) | (678) | (1,866) | 117,172 |
| Total cost of intangible assets | 4,003,893 | 85,882 | 3,183 | (2,273) | (86,209) | 4,004,476 |
| Accum. amort. of development costs | (199,444) | (32,694) | — | — | 3,306 | (228,832) |
| Accum. amort of concessions, patents, licences, br. | (77,331) | (16,274) | 363 | 192 | 1,554 | (91,496) |
| Accum. amort. of cumputer software | (220,305) | (34,366) | (1,294) | 104 | 4,423 | (251,438) |
| Accum. amort. of currently marketed products | (464,094) | (51,484) | — | — | 16,231 | (499,347) |
| Accum. amort. of other intangible assets | (91,489) | (12,391) | — | 678 | 3,094 | (100,108) |
| Total accum. amort intangible assets | (1,052,663) | (147,209) | (931) | 974 | 28,608 | (1,171,221) |
| Impairment of other intangible assets | (2,083) | (421) | — | 1,438 | 7 | (1,059) |
| Carrying amount of intangible assets | 2,949,147 | (61,748) | 2,252 | 139 | (57,594) | 2,832,196 |
This appendix forms an integral part of Nota 7 to the consolidated annual accounts.
(expressed in thousands of Euros)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| Balance at 31/12/2023 |
Additions | Transfers | Disposals | Translation differences |
Balance at 31/12/2024 |
|
|---|---|---|---|---|---|---|
| Land and buildings | 1,216,059 | 71,698 | 505 | (21,369) | 58,094 | 1,324,987 |
| Machinery | 7,693 | 854 | (120) | (167) | 365 | 8,625 |
| Computer equipment | 4,221 | 852 | — | (745) | 199 | 4,527 |
| Vehicles | 22,216 | 5,646 | — | (3,100) | 555 | 25,317 |
| Total cost of rights of use | 1,250,189 | 79,050 | 385 | (25,381) | 59,213 | 1,363,456 |
| Accum. depr. of land and buildings | (282,755) | (74,929) | (505) | 5,206 | (15,387) | (368,370) |
| Accum. depr. of machinery | (3,975) | (1,522) | 120 | 164 | (239) | (5,452) |
| Accum. depr. of computer equipment | (3,457) | (559) | — | 710 | (189) | (3,495) |
| Accum. depr. of vehicles | (14,762) | (5,106) | — | 2,498 | (465) | (17,835) |
| Total accum. Depr. of rights of use | (304,949) | (82,116) | (385) | 8,578 | (16,280) | (395,152) |
| Carrying amount of rights of use | 945,240 | (3,066) | — | (16,803) | 42,933 | 968,304 |
This appendix forms an integral part of Note 8 to the consolidated annual accounts.
(expressed in thousands of Euros)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| Balance at 31/12/2022 (*) |
Additions | Transfers | Disposals | Translation differences |
Balance at 31/12/2023 (*) |
|
|---|---|---|---|---|---|---|
| Land and buildings | 1,198,363 | 94,699 | (1,957) | (41,103) | (33,943) | 1,216,059 |
| Machinery | 6,664 | 2,871 | (1,008) | (658) | (176) | 7,693 |
| Computer equipment | 6,819 | 597 | (2,484) | (604) | (107) | 4,221 |
| Vehicles | 20,958 | 4,737 | (79) | (3,191) | (209) | 22,216 |
| Total cost of rights of use | 1,232,804 | 102,904 | (5,528) | (45,556) | (34,435) | 1,250,189 |
| Accum. depr. of land and buildings | (229,605) | (71,157) | 1,957 | 8,830 | 7,220 | (282,755) |
| Accum. depr. of machinery | (3,647) | (1,507) | 523 | 590 | 66 | (3,975) |
| Accum. depr. of computer equipment | (5,793) | (860) | 2,516 | 580 | 100 | (3,457) |
| Accum. depr. of vehicles | (12,499) | (5,019) | 45 | 2,506 | 205 | (14,762) |
| Total accum. Depr. of rights of use | (251,544) | (78,543) | 5,041 | 12,506 | 7,591 | (304,949) |
| Carrying amount of rights of use | 981,260 | 24,361 | (487) | (33,050) | (26,844) | 945,240 |
(*) Restated figures (Note 2.d)
This appendix forms an integral part of Note 8 to the consolidated annual accounts.
(expressed in thousands of Euros)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| Balance at 31/12/2023 |
Additions | Transfers | Disposals | Translation differences |
Balance at 31/12/2024 |
|
|---|---|---|---|---|---|---|
| Cost: | ||||||
| Land and buildings | 1,131,912 | 379 | 56,480 | (4,453) | 46,289 | 1,230,607 |
| Plant and machinery | 3,175,459 | 66,772 | 263,393 | (78,230) | 127,055 | 3,554,449 |
| Fixed Assets under construction | 910,670 | 193,159 | (323,173) | — | 21,657 | 802,313 |
| 5,218,041 | 260,310 | (3,300) | (82,683) | 195,001 | 5,587,369 | |
| Accumulated depreciation: | ||||||
| Buildings | (206,375) | (31,505) | 57 | 1,481 | (9,807) | (246,149) |
| Plant and machinery | (1,757,723) | (190,599) | (177) | 31,039 | (74,857) | (1,992,317) |
| (1,964,098) | (222,104) | (120) | 32,520 | (84,664) | (2,238,466) | |
| Impairment of other property, plant and equipment |
(6,820) | (1,370) | — | 1,120 | 13 | (7,057) |
| Carrying amount | 3,247,123 | 36,836 | (3,420) | (49,043) | 110,350 | 3,341,846 |
This appendix forms an integral part of to the consolidated annual accounts.
(expressed in thousands of Euros)
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
| Balance at 31/12/2022 (*) |
Additions | Business combination |
Transfers | Disposals | Translation differences |
Balance at 31/12/2023 (*) |
|
|---|---|---|---|---|---|---|---|
| Cost: | |||||||
| Land and buildings | 1,155,406 | 6,046 | — | 342 | (4,953) | (24,929) | 1,131,912 |
| Plant and machinery | 3,103,209 | 72,241 | 480 | 125,507 | (58,245) | (67,733) | 3,175,459 |
| Fixed Assets under construction | 879,542 | 183,044 | — | (125,460) | (1,646) | (24,810) | 910,670 |
| 5,138,157 | 261,331 | 480 | 389 | (64,844) | (117,472) | 5,218,041 | |
| Accumulated depreciation: | |||||||
| Buildings | (181,337) | (32,309) | — | 181 | 1,954 | 5,136 | (206,375) |
| Plant and machinery | (1,641,398) | (188,361) | (383) | (2,336) | 34,705 | 40,050 | (1,757,723) |
| (1,822,735) | (220,670) | (383) | (2,155) | 36,659 | 45,186 | (1,964,098) | |
| Impairment of other property, plant and equipment |
(12,564) | (1,173) | — | — | 6,767 | 150 | (6,820) |
| Carrying amount | 3,302,858 | 39,488 | 97 | (1,766) | (21,418) | (72,136) | 3,247,123 |
(See Note 3)
(*) Restated figures (Note 2.d)
This appendix forms an integral part of to the consolidated annual accounts.
The management report for the year ended December 31, 2024, should be read in conjunction with the consolidated financial statements for the same period and related notes. The comments and analyses included in the report may contain forward-looking statements and considerations that involve risks and uncertainties - in this regard, please refer to the legal notice included at the end of the Consolidated Non-Financial Information and Sustainability Statement for fiscal year 2024, specifically the "Main Risks" section in the "Risk Management and Control" section of the Governance chapter.
For Grifols, 2024 was a year of significant events and record growth. The company closed a decisive year in financial performance and achievements, while remained focused on executing on its strategy, implementing several initiatives to transform the company: strengthening corporate governance and executive management; focusing on financial discipline; reinforcing a culture of performance and accountability; and ultimately, achieving our financial and operational targets with a focus on increasing cash flow generation.
In this context, Grifols' revenue reached a record EUR 7,212 million, representing an increase of 10.3% cc1 (+9.4% reported2 ).
Biopharma's revenues increased by 11.3% cc (+10.5% reported) to EUR 6,143 million in 2024. The main growth levers were the solid performance of key proteins in key markets driven by robust underlying demand and a favorable product mix. Worth noting is the robust sales growth of immunoglobulins, representing around 60% of Biopharma revenues. Sales grew by 15.3% cc, fueled by strong demand for intravenous immunoglobulin (IVIG) and the significant growth of subcutaneous immunoglobulin (SCIG) Xembify® at 55.5% in key markets such as the United States and EU.
In 2024, Grifols continued to strengthen its immunoglobulin franchise by focusing its efforts on the fastest-growing immunodeficiency segments, including primary (PID) and secondary (SID) immunodeficiencies, while maintaining its leadership in neurology and intensive care. The company aspires to continue to drive the growth of this franchise in the U.S. and prioritize certain countries, while accelerating the expansion and penetration of Xembify® , for which demand continues to increase in geographies quarter-over-quarter.
Sales of albumin grew by 8.0% cc, driven mainly by demand in China and US, and the solid performance in main European countries. In addition, Grifols' innovative sales strategy under the SRAAS agreement leads to greater supply in the country. Alpha-1 and other specialty proteins grew by +4.9% cc, with the former affected by the specialty pharma distributor transition but showing an uptick in the fourth quarter. Demand for hyperimmune immunoglobulins in the U.S. was also strong.
In 2024, Diagnostic recorded revenues of EUR 645 million in 2024, up 0.7% cc excluding the 19 million commercial one-off that took place in the first quarter of 2023. Including this, the Business Unit declined by 2.1% cc (-3.8% reported).
Blood typing solutions (+14.3%) continued to be the main driver, with growth across main countries, including the U.S., LATAM and EMEA.
1 Operating or constant exchange rate (cc) excludes exchange rate variations for the period
2 Reported includes the impact of foreign exchange rates
Bio Supplies grew by 35.3% cc (+34.8% reported) to EUR 216 million. The year represent significant growth in the business through capitalizing on its momentum and maximizing the value of its product portfolio.
Grifols continues to efficiently manage its plasma supply and reduce its cost per liter (CPL), leading to significant increases in profit margins. Significant effort was placed in 2024 to meet the increasing demand for products while simultaneously managing inventory levels to effectively grow the business while optimizing consumption of working capital. The improvements quarter-over-quarter and sequentially throughout the year highlights this progress. Another highlight is the implementation of more efficient plasmapheresis equipment to increase yield. On this regard, the pilot on the nomogram technology kicked off in 2024.
The company currently operates the largest private plasma supply network in the world. Approximately one quarter of all donor centers are outside the U.S. This is the largest network of donor centers ex-US within the industry – the recent expansion of donor centers in Egypt and Canada are key to growth supplementing the large number of donor centers in Germany and Eastern EU.
In 2024, gross margin increased to 38.7% (37.8% in 2023), driven by strong revenue growth, product mix and lower cost per liter of plasma (CPL) as a result of the Operational improvement plan, considering the approximate ninemonth lag in inventory accounting in the plasma industry.
Adjusted EBITDA reached EUR 1,779 million, representing a margin of 24.7% on revenues, improving significantly compared to 22.2% in 2023. Reported EBITDA stood at EUR 1,631 million (22.6% margin). The sequential expansion EBITDA throughout the year was supported by the growth of Biopharma, cost savings stemming from the operational improvement plan and operating leverage.
The financial result stood at EUR 748 million loss in 2024 (EUR 574 million loss in 2023).
Reported net income was positive at EUR 157 million in 2024 (EUR 42 million in 2023).
On December 31, 2024, total assets stood at EUR 21,405 million, compared with EUR 20,992 million on December 31, 2023.
Inventories remained stable at EUR 3,560 million with a turnover of 294 days (309 days in December 2023) due to the progressive impact of the improved cost per liter of plasma in a context of increased supply. Average collection and payment periods remained stable at 36 days (36 days in 2023) and 61 days (57 days in 2023). The average payment period to suppliers of the Spanish group companies was 71 days, similar to the previous year's average of 71 days (all these figures include Biotest except for average payment period). For more information regarding Grifols' supplier payment practices, see the section "Political commitment and activities with advocacy groups" in the Governance chapter in the Consolidated Non-Financial Information and Sustainability Statement for fiscal year 2024.
Improvements in working capital management continue to optimize Grifols' financial structure. As of December 31, 2024, working capital consumption stood at EUR 22 million mainly driven by a strong fourth quarter.
Deleveraging remains a core priority for Grifols, which reiterates its aim of reducing debt on its balance sheet. At the close of 2024, the debt ratio fell to 4.6x (6.4x in December 2023; under the Credit Agreement, see reconciliations in the Annex) following an uptick in EBITDA and operating cash flow generation, which stood at EUR 902 million in 2024
Including the sale of SRAAS share capital to Haier Group, the issuance of private placement notes and extension of the RCF, Grifols continues to advance in its deleveraging path.
On December 31, 2024, shareholder equity totaled EUR 5,107 million. Grifols' share capital is represented by 426,129,798 ordinary shares (Class A), with a nominal value of EUR 0.25 per share, and 261,425,110 non-voting shares (Class B), with a nominal value of EUR 0.05 per share.
Grifols ordinary shares (Class A) are listed on the Spanish Stock Market and form part of the IBEX-35 (GRF) and non-voting shares (Class B) are listed on the Spanish Stock Market (GRF.P). Grifols Class A and B shares are also listed on NASDAQ (GRFS) through ADRs (American Depositary Receipts).
Cash flow generation in 2024 was driven by a strong fourth quarter. The robust performance was due to active and efficient management of working capital, including inventory, accounts receivables and payables. Financial discipline in CAPEX spend also contributed.
In 2024, net cash flows from operating activities continued their positive trend fueled by solid business performance and the effective implementation of the operational improvement plan announced at the onset of 2024. Operating cash flows reached EUR 902 million (EUR 219 million in 2023).
Net cash flows from investment activities including the proceeds from the sale of SRAAS, totaled EUR 887 million, the most significant of which was capital expenditures (CAPEX). These were focused primarily on Biopharma's new production facilities, of note investments in the plasma fractionation, immunoglobulin purification and albumin plants in Montreal (Canada), as well as in the new albumin plant in Dublin.
Cash flow from financing activities totaled -EUR 1,359 million comprised primarily of the repayment and redemption of senior secured notes and term loans offsetting the new private placement notes.
On December 31, 2024, Grifols' net financial debt was EUR 8,046 million, excluding the impact of IFRS 163 .
3 At December 31, 2024, the impact of the application of IFRS 16 on debt is EUR 1,141 million
In 2024, the company has continued to actively reduce its debt ratio both organically through EBITDA improvement and inorganically through divestments of SRAAS. As part of its inorganic debt reduction strategy, Grifols completed sale of and strategic alliance with Haier Group, which includes the sale of ~20% of SRAAS capital for USD 1,800 million.
As of December, 2024, the company's net financial debt to EBITDA ratio stood at 4.6x in accordance with the Credit Agreement (see Annex for reconciliation).
Furthermore, in 2024 Grifols continued to optimize its financial structure. At the close of this report, close to 70% of Grifols' debt is linked to fixed interest rates. While there are no significant debt maturities before 2027 and no periodic financial covenants, this financial structure lessens the impact of interest rate rises.
Grifols repaid its 2025 debt maturities mainly by using the proceeds from the SRAAS divestment, and issuance of private placement notes. With the support of its main banks, the company has marked a clear path to fulfil its expected maturities, while remaining steadfast in its pledge to meet its debt reduction targets.
On April 23, 2024, Grifols successfully completed a EUR 1 billion private placement of senior secured notes. The transaction closed with an annual coupon of 7.5% and maturity in May 2030. The Senior Secured Notes have a purchase price of 98.50% of the principal amount. The proceeds were used to redeem Grifols' Senior Unsecured Notes due in May 2025. In conjunction to this, the company also successfully closed the issuance of additional EUR 300 million private placement secured notes. This amount is in addition to the initial EUR 1 billion private placement completed and has the same economic terms
On December 19, 2024, Grifols successfully completed another private placement of EUR 1.3 billion of 7.125% senior secured notes maturing in May 2030 issued at par. The proceeds from this placement were used to redeem Grifols' 1.625% Senior Secured Notes due in February 2025, fully repay the outstanding revolving loans maturing in November 2025, and for general corporate purposes. Taken as a whole, these transactions were leverage-neutral. In conjunction with these offerings, Grifols also entered into an agreement to partially extend and upsize its Revolving Credit Facility (RCF) through May 2027. These transactions successfully concluded Grifols' efforts to significantly deleverage its balance sheet, proactively manage all its debt maturities, and strengthen its overall liquidity position.
In 2024, Grifols advanced its capital investment plan to expand and improve the production facilities of its business units. The company has greatly optimized its CAPEX resource allocations considering the investments already made in recent years. In 2024, capital expenditures related to Property, Plant and Equipment (PP&E) additions stood at EUR 232 million (EUR 224 million in 2023). The investments in 2024 and prior have well positioned the company to satisfy growth and expansion.
On June 18, 2024 Grifols completed the sale of a 20% equity stake in Shanghai RAAS (SRAAS) to Haier Group Corporation (Haier Group) and forged a strategic alliance with Haier Group. The alliance leverages synergies between Grifols' industry-leading plasma and diagnostic excellence and Haier Group's preeminent portfolio of healthcare solutions to innovate and contribute to SRAAS' growth in the long run. In the terms of the share purchase agreement, Grifols sold a 20% equity stake in SRAAS to Haier Group for RMB 12.5 billion (approximately EUR 1.6 billion) cash consideration. Grifols retains a 6.58% economic stake in SRAAS as well as a seat on its Board of Directors.
The two companies extend their exclusive albumin distribution agreement through the next 10 years – with guaranteed minimum volumes between 2024 and 2028 – and SRAAS has the option to prolong it through 2044. China's demand for albumin is significant and the demand remains significant in the coming years. The full proceeds from the transaction were used to repay debt as part of the company's path to reduce leverage.
On July 7, 2024, the Board of Directors of the Company received a request from the Grifols family members (the "Family Shareholders") and Brookfield Capital Partners (UK) Limited ("Brookfield") to allow for access to certain information of the Company to carry out a due diligence process with respect to an acquisition of shares of Grifols. It was informed that the intent of the transaction, if the case went through, it would mean the delisting of the Company.
On November 19, 2024, based on the recommendation of its Transaction Committee within the Board of Directors, it did not recommend to shareholders of the company to accept a potential offer from Brookfield with a valuation of €6.45 billion for the entirety of the company's outstanding share capital (comprising both Class A and Class B shares). This indicative, non-binding valuation from Brookfield implied a price of €10.50 per Class A share and €7.62 per Class B share, which was deemed to significantly undervalue the company's fundamental prospects and long-term potential. This assessment is supported by the company's robust financial performance, which demonstrate Grifols' strong fundamentals and its ability to capture substantial global demand across key markets. This announcement comes after a comprehensive due diligence exercise has been conducted, with Brookfield granted access to all requested information.
On November 27, 2024, Grifols announced the termination of discussions with Brookfield Capital Partners (UK) Limited ("Brookfield") regarding a potential acquisition of Grifols shares.
In September 2024, Thomas Glanzmann, as Executive Chairperson, transitioned to a non-executive role. This is another step in the previously announced governance enhancements, which we first began in 2022; and allows Mr. Glanzmann to fully dedicate his time to the non-executive chairmanship role.
In February 2024, it was announced that Raimon Grifols and Víctor Grifols Deu decided to transition out of their respective executive positions and remain on the Grifols Board, now as proprietary directors. The moves were part of a long-planned, carefully architected corporate governance evolution strategy that Raimon Grifols and Víctor Grifols Deu initiated in 2022, together with the Board, to steadily separate ownership from company Management.
In February 2024, Nacho Abia was appointed as a member of the Board and assuming the role of CEO in April 2024. Mr. Abia is a seasoned senior executive with 25 years of international management experience at publicly traded lifescience and medical-technology companies. He was most recently Executive Officer and Global Chief Strategy Officer of Tokyo-based Olympus Corporation, a Nikkei-listed company with 33,000 employees that specializes in medical technology and is a global leader in diagnostics and minimally invasive treatments. Mr. Abia was responsible for Corporate Strategy and Planning, Business Development and Global Operating Model, with all Olympus regional presidents reporting to him. Prior to that he was Executive Officer and Global Chief Operating Officer, responsible for all Olympus vertical divisions including Endoscopic Solutions, Therapeutic Solutions and Scientific Solutions, with combined revenues of more than USD 7 billion.
In the second quarter of the year, board member Carina Szpilka announced her retirement from the Board to pursue other personal and professional endeavors requiring her full dedication,
On April 2024, the Board accepted the resignation submitted by the Board member Mr. Tomás Dagá Gelabert to his office as Secretary non-member of the Audit Committee, with immediate effect. Mr. Tomás Dagá Gelabert continues as member of the Grifols' Board; and appoint, Ms. Laura de la Cruz Galán, as Secretary non-member of the Audit Committee, in substitution of Mr. Tomás Dagá Gelabert.
On June 14, 2024, the Annual General Meeting was held, shareholders voted to increase the number of members of the Board of Directors to 13; re-elect the company's independent auditors for fiscal years 2024-2026 and appoint Deloitte as verifier of sustainability information; approve the company's individual and consolidated financial statements, as well as the consolidated statement of non-financial information; approve, on a consultative basis, the Annual Compensation Report; and modify the remuneration policy of the company's directors.
On July 16, 2024, the Company's Board of Directors, unanimously agreed to resolve the following: To appoint Mrs. Montserrat Muñoz Abellana as new Lead Independent Director of the Company's Board of Directors; (b) appoint Mrs. Anne-Catherine Berner as new member of the Audit Committee; To appoint Mrs. Anne-Catherine Berner as new Chairperson of the Appointments and Remuneration Committee; and To appoint Mrs. Enriqueta Felip Font as new member of the Appointments and Remuneration Committee. Also, Board member Claire Giraut announced she was stepping down from her role due not having time and resources to dedicate to the Board during the time.
In December 2024 Grifols' Board of Directors announces that during its meeting, it unanimously agreed to appoint Mr. Pascal Ravery and Mr. Paul S. Herendeen as new members of the Board of Directors through the co-option procedure, thereby filling the two existing vacancies. Mr. Pascal Ravery will serve as an independent director, while Mr. Paul S. Herendeen will serve as a proprietary director. The appointment of Mr. Paul S. Herendeen follows the request received by the Company from several minority shareholders (FF Hybrid LP, Flat Footed Series LLC-Fund3, GP Recovery Fund LLC, Mason Capital Master Fund, and Sachem Head LP), who have grouped their shares in accordance with the applicable law to exercise their proportional representation right and requested the appointment of Mr. Paul S. Herendeen as a Board member.
Grifols requires a robust team and strong leadership to fully realize its potential and consolidate its leadership in the plasma industry. To this effect, Grifols appointed of new senior executives included:
audit & assurance services, transaction services and corporate finance, mergers and acquisitions and capital markets.
In July, the seven-year agreement was executed between Biotest and Kedrion. The agreement is forecasted to add approximately USD 1 billion in revenue from sales in the United States of its intravenous immunoglobulin (Ig) Yimmugo®, following recent Food and Drug Administration (FDA) approval to treat primary immunodeficiencies (PID). Yimmugo is the first Biotest medicine to be commercialized in the U.S. from its new FDA-certified "Next Level" production facility in Dreieich, Germany. This Ig is already approved for production and marketing in Europe, where Yimmugo has been commercialized since late 2022.
Grifols' innovation pipeline continues to make solid progress focusing on product lifecycle management and new proteins and indications. Fueled by internal research and external innovation, the company achieved its milestones set for 2024, including the Yimmugo FDA approval, Xembify bi-weekly dosing approval, and Fibrinogen regulatory submission, among others.
Biotest trials also continue gaining ground. In February 2024, Grifols announced positive results from Biotest's ADFIRST Phase 3 clinical trial for fibrinogen concentrate, marking significant headway in treating acquired fibrinogen deficiency. The trial achieved its primary goal, demonstrating efficacy equivalent to standard care and an excellent safety profile. It is as effective as standard of care in reducing intraoperative blood loss in patients with AFD. Regulatory submission documents completed in both the EU and US. The expected market launches are in the second half of 2025 in EU and beggining of 2026 in the US. This positions the fibrinogen concentrate to becoming the first fibrinogen concentrate approved for Acquired Fibrinogen Deficiency in the U.S., accessing a global market with significant potential.
Topline results were released. Although the trial did not meet its primary endpoint of one-year transplant-free survival, an improvement in transplant-free survival, mortality and disease-related complications was observed for patients treated with Albutein 20% plus standard medical treatment (SMT) compared with patients receiving only SMT. Further, a notable improvement in time-to-liver transplant or death at three months was observed for the study treatment plus SMT group of patients, when compared with the patients treated only with SMT. The safety and tolerability profile was favorable, and there were no adverse-reaction risks, beyond what is already on label, that would limit adoption of the therapy. Grifols plans to present complete study results at the May 2025 EASL (European Association for the Study of the Liver) Congress.
GigaGen has received a BARDA contract of up to \$135 million to develop a recombinant ("synthetic") polyclonal therapeutic for all seven serotypes of BoNTs, as well as a second biothreat to be determined at a later time. GigaGen is the only company in the world developing highly diverse, recombinant polyclonal therapies. The contract will support the creation, manufacturing and initial clinical development of a drug product that targets all seven BoNT variants and a second biothreat.
The transactions carried out with treasury stock during 2024 are set out in the notes to the consolidated financial statements in Note 17(d) attached to this report. As of December 31, 2024, Class A treasury shares totaled 3,944,430 and Class B treasury shares amounted to 3,201,374 shares.
Detailed information in the consolidated financial statements in Note 30 attached to this report.
Subsidies received by Grifols correspond mainly to initiatives related to employee training and job creation.
| Subsidies | |
|---|---|
| Spain | 494 thousand of euros |
| U.S. | 18,292 thousand of euros |
Grifols' Annual Corporate Governance Report for the 2024 fiscal year forms part of the Management Report. As of the date of publication of the consolidated annual accounts, it is available on the CNMV website and on Grifols' website.
Grifols' Annual Directors' Remuneration Report for the year 2024 forms part of the Directors' Report. As of the date of publication of the consolidated annual accounts, it is available on the CNMV website and on Grifols' website.
In accordance with the provisions set forth in Law 11/2018, of December 28, regarding non-financial information and diversity, the Group has prepared the Non-Financial Information Statement for the fiscal year 2024. The Board of Directors of Grifols, S.A. prepares the Consolidated Non-Financial Information and Sustainability Statement for the year 2024 as a separate document and an integral part of the Consolidated Director's Report and as a separate document from the consolidated financial statements.
This report includes the impact of the group's activity with respect to environmental and social issues; respect for human rights; initiatives relating to the fight against corruption and bribery; and those relating to personnel, including any measures adopted to promote the principle of equal treatment and opportunities between women and men, non-discrimination and inclusion of people with disabilities and accessibility.
In addition to the subsequent events in Note (34) of the Group's Consolidated Financial Statements, there are no additional relevant subsequent events that are relevant to add.
Building on our strong foundations and clear momentum, the management team is executing on its Strategic Plan focused on profitable growth, margin expansion, cash flow generation and disciplined capital allocation to unlock Grifols' full potential. Biopharma will continue to be the main growth engine, levering on commercial excellence by broadening our portfolio, capitalizing on the most diversified plasma sourcing model in the industry, a strong innovation pipeline focused, and increasing yields and efficiencies throughout the value chain.
Promoting sustainability continues to be the cornerstone of Grifols' long-term business model with environmental, social and corporate governance (ESG) at its core.
In its quest for sustainable growth and further strengthening its robust industry status, the company raised its excellence in ESG practices. As the company advances its sustainability goals, it remains focused on driving longterm value and making a lasting impact toward a more sustainable, ethical and resilient future for all stakeholders.
In 2024, Grifols has allocated a total of 44.2 million euros to environmental management, an increase of 35% compared to 2023. Over the last three years, the total investment has been 111 million euros. Of the €15.8 million invested in environmental assets, 39% has been allocated to eco-efficiency, another 39% to the water cycle, 2% to waste management and 20% to other projects. Environmental expenditures amounted to 28.3 million euros, with 72% devoted to waste management. This significant financial effort reflects Grifols' commitment to the continuous improvement of its environmental performance and its progress in complying with the 2023-2026 Environmental Program.
The company has reaffirmed its commitment to the quality of employment and the well-being of its human resources. The total workforce reached 23,822 employees, with 57% women and 43% men. In total, 5,867,705 hours of training were given, with a high level of participation. In addition, Grifols maintains a zero-tolerance policy towards discrimination and harassment, ensuring an inclusive and safe working environment. In this regard, in 2024, 65 affirmative action measures were implemented. In addition, 3.8% of the workforce was made up of people with disabilities. Grifols continues to advance in its commitment to equality and equity, reviewing promotion processes, using inclusive language and supporting women at risk of exclusion. In the company, 40% of women hold senior management positions, and have accounted for 60% of promotions and 65% of new hires.
Grifols was ranked as the number one biotechnology company in the S&P Dow Jones Sustainability Indices (DJSI), ascending to the top position in its fifth straight year of inclusion in the prestigious indices. This recognition strengthens Grifols' stature as a global leader in sustainability practices and comes as the company achieved its highest-ever S&P Global Corporate Sustainability Assessment (CSA) score. Grifols earned a rating of 70 points, marking a seven-point increase over last year's results and highlighting the company's significant progress and unwavering commitment to sustainability.
The company was awarded a Gold Medal by EcoVadis, a leading global corporate sustainability rating platform, for the second consecutive year. Achieving a score of 77 out of 100, Grifols is positioned in the 97th percentile, showcasing its leadership in sustainability.
| FY 2024 | FY 2023 | % VS PY | ||
|---|---|---|---|---|
| Grifols Grifols |
Grifols Combined | |||
| In thousands of euros | Reported | At cc* | ||
| Revenue by Business Unit | 7,212,382 | 6,591,977 | 9.4% | 10.3% |
| Biopharma | 6,142,588 | 5,558,301 | 10.5% | 11.3% |
| Diagnostic | 644,898 | 670,269 | (3.8%) | (2.1%) |
| Bio Supplies | 215,664 | 159.957 | 34.8% | 35.3% |
| Others & intersegments | 209,232 | 203,450 | 2.8% | 3.5% |
| Revenue by Country | 7,212,382 | 6,591,977 | 9.4% | 10.3% |
| US + CANADA | 4,087,030 | 3,898,961 | 4.8% | 5.6% |
| EU | 1,498,898 | 1,255,927 | 19.3% | 19.4% |
| ROW | 1,626,455 | 1,437,089 | 13.2% | 15.1% |
To complement the consolidated financial statements presented in accordance with International Financial Reporting Standards (IFRS), Grifols provides the following tables and reconciliations. These tables contain APM measures, which are used in conjunction with financial metrics in accordance with IFRS. Their purpose covers budget setting, business management, operational and financial performance evaluation, as well as comparison with prior periods and competitors. The inclusion of these measures is useful as it allows for analysis and comparison of profitability and solvency across companies and industries, eliminating accounting and financial effects that are not directly related to cash flows.
In addition, Grifols presents non-financial measures because they are commonly used by investors, securities analysts, and other market players. These measures complement the analysis of financial performance and should be considered in conjunction with IFRS metrics, not as a replacement for them.
The following tables set out the measures and ratios commonly used by Grifols, including their name, purpose and, in the case of ratios, how they are calculated.
| Alternative Performance Measures | Definition | Aim / Purpose |
|---|---|---|
| Revenue at constant currency | Reported revenue + variation due to exchange rate impact |
Excludes fluctuations in the exchange rates of the different currencies in which Grifols reports revenues in order to facilitate to facilitate the comparison between different financial periods and the understanding of their evolution. |
| Earnings Before Interest, Tax, Depreciation and Amortization (EBITDA) or Gross Operating Profit |
Operating profit + depreciation, amortization and provisions |
El EBITDA ("Earnings Before Interest, Tax, Depreciation and Amortization") evaluates operating results without taking into account large expense items that have no impact on cash flows. This metric provides a more accurate and comparable understanding of the company's performance. |
| EBITDA adjusted | Same as above + extraordinary costs - extraordinary revenues |
More accurately reflects the company's organic performance, including or excluding certain non-recurring amounts, see detail below: |
|---|---|---|
| For more information about these extraordinary amounts, see reconciliation tables below. |
- Restructuring costs: in 2023 and 2024 the company incurred a set of extraordinary costs in order to significantly reduce its cost structure following the impact of COVID-19. |
|
| In this regard, in 2022 the company implemented a comprehensive operational improvement plan ("Operational Improvement Plan") designed to strengthen its competitiveness and create a leaner and more efficient organization. This plan is estimated to achieve annual cost savings of more than 450 million euros. The result of this initiative translates into a significant reduction in the company's total cost base, an improvement in its operating cash flow, and the establishment of a more dynamic and efficient operating model. |
||
| This is the first time the company has implemented such a plan. These impacts have been considered of a non-recurring nature because it is not a plan that is carried out on an annual basis, as well as for its own extraordinary nature. |
||
| In 2023, a restructuring impact related to this Operational Improvement Plan is recorded, totaling €159 million, €20 million being in the fourth quarter. In 2024, this amounted to €36m. |
||
| - Transaction costs: in 2023, transaction costs are related to the strategic transaction in China with Haier Group, through which it will sell approximately a 20% stake in Shanghai RAAS to Haier for approximately USD 1.8 billion. The extraordinary nature of this transaction must be taken into account in the context of the company's leverage. Mainly linked to this, in 2024 we accounted transaction costs of €49m |
||
| -Impairments: in 2023 it refers to an impairment in "Others" business unit. In 2024, it is linked with Biopharma. |
||
| -Biotest Next Level (BNL) project: this refers to a specific project aimed at increasing Biotest's production capacity in Dreieich, Germany. |
1.
| It has been decided to adjust the costs strictly related to this project due to the extraordinary and non-recurring nature of this project due to the high investment in terms of operating expenses required to start up the company's production facilities. Failure to adjust for this impact would distort the picture of the company's level of recurring operating expenses. Other Non-Recurring Items: most of these one-offs were related to costs as a consequence of the short-seller attack. |
||
|---|---|---|
| EBITDA adjusted 12M | EBITDA calculated considering the last 12 months |
To make comparable periods that do not necessarily coincide with the closing months of the fiscal year. Refer to the term "adjusted" to the immediately preceding point. |
| EBITDA adjusted as per Credit |
Definition established in the Grifols | Measure used to calculate the leverage |
|---|---|---|
| Agreement | Credit Agreement. defined as net | ratio. |
| income on a consolidated basis for the | ||
| Group, plus (i) all financial results, | ||
| (ii) any losses on ordinary course | ||
| hedging obligations, (iii) any foreign | ||
| currency translation, transaction or | ||
| exchange losses, (iv) any loss of any | ||
| equity-accounted investee, (v) tax |
||
| expense, (vi) depreciation, (vii) |
||
| amortization, write-offs, write-downs, | ||
| and other non-cash charges, losses | ||
| and expenses, (viii) impairment of | ||
| intangibles, (ix) non-recurring losses, | ||
| (x) transactions costs, (xi) |
||
| extraordinary, unusual, or non |
||
| recurring charges and expenses |
||
| including transition, restructuring and | ||
| "carveout" expenses, (xii) any costs | ||
| and expenses relating to the Issuer's | ||
| potential or actual issuance of Equity | ||
| Interests and (xiii) the amount of cost | ||
| savings, adjustments, operating |
||
| expense reductions, operating |
||
| improvements and synergies, in each | ||
| case on a "run rate" basis and in | ||
| connection with acquisitions, |
||
| investments, restructurings, business | ||
| optimization projects and other |
||
| operational changes and initiatives; | ||
| less (i) interest income, (ii) non | ||
| recurring gains, (iii) any income or | ||
| gains on ordinary course hedging | ||
| obligations (iv) foreign currency |
||
| translation, transaction or exchange | ||
| gains and (v) any income of any | ||
| equity-accounted investee, in each | ||
| case, for the last 12 months. | ||
| EBIT (Earnings Before Interest and | Revenue – operating expenses | Measures profitability and reflects |
| Taxes) | earnings before interest expense and | |
| taxes |
| Net financial debt as per Credit Agreement |
Definition established in the Grifols Credit Agreement. Amount by which Grifols's total financial liabilities exceed its total financial assets, including cash and cash equivalents. It excludes the impact of IFRS 16, which specifies how an IFRS reporter will recognize, measure, present and disclose leases. |
Measure used to calculate the leverage ratio. |
|---|---|---|
| Non-current financial liabilities – Non-recurrent lease liabilities (IFRS16) + Current financial liabilities – Current lease liabilities – Cash and cash (IFRS16) equivalents |
||
| Leverage ratio | Net financial debt as per Credit Agreement / EBITDA adjusted 12M as per Credit Agreement |
Measure of the company's ability to repay its debt based on the company's operating income, based on EBITDA, without taking into net financial results, taxes, depreciation and amortization. |
| R&D net investment | R&D current expenses in P&L + R&D capitalized – R&D depreciation, amortization and write-offs + R&D CAPEX fixed assets + R&D external |
A more accurate reflection of the resources that the company is allocating to its research and development activities. Excludes capitalizations and amortizations associated with research and development (R&D) projects. |
| Total PP&E additions | Property, Plant and Equipment (PP&E) additions ("Reported CAPEX") + interest capitalized |
Breaks down the cash flow that the company invests in its productive capacity, as well as increases in productivity and efficiency in its processes. |
Consolidated Director's Report for the year ended
For reconciliation purposes, detailed information is provided below.
| In thousands of euros | 2024 | 2023 | % Var |
|---|---|---|---|
| Reported Net Revenues | 7,212,382 | 6,591,977 | 9.4% |
| Variation due to Exchange Rate Effects | 58,550 | ||
| Net Revenues at Constant Currency | 7.270.932 | 6,591,977 | 10.3% |
| In thousands of euros | 2024 | 2023 | % Var |
| Reported Biopharma Net Revenues | 6.142.588 | 5,558,301 | 10.596 |
| Variation due to Exchange Rate Effects | 45,143 | ||
| Reported Biopharma Net Revenues at Constant Currency | 6.187.731 | 5,558,301 | 11.3% |
| In thousands of euros | 2024 | 2023 | % Var |
| Reported Diagnostic Net Revenues Variation due to Exchange Rate Effects |
644,898 11,360 |
670,269 | (3.896) |
| Reported Diagnostic Net Revenues at Constant Currency | 656,258 | 670.269 | (2.1%) |
| In thousands of euros | 2024 | 2023 | % Var |
| Reported Bio Supplies Net Revenues | 215,664 | 159,957 | 34.8% |
| Variation due to Exchange Rate Effects | 753 | ||
| Reported Bio Supplies Net Revenues at Constant Currency | 216,417 | 159.957 | 35.3% |
| In thousands of euros | 2024 | 2023 | % Var |
| Reported Others & Intersegments Net Revenues | 209,232 | 203,450 | 2.8% |
| Variation due to Exchange Rate Effects | 1,294 | ||
| Reported Other & Intersegments Net Revenues at Constant Currency | 210.526 | 203.450 | 3.5% |
| In thousands of euros | 2024 | 2023 | % Var |
| Reported U.S. + Canada Net Revenues | 4,087,030 | 3,898,961 | 4.8%6 |
| Variation due to Exchange Rate Effects | 30,222 | ||
| Reported U.S. + Canada Net Revenues at Constant Currency | 4.117.252 | 3.898.961 | 5.6% |
| In thousands of euros | 2024 | 2023 | % Var |
| Reported EU Net Revenues | 1.498.898 125 |
1,255,927 | 19.3% |
| Variation due to Exchange Rate Effects | |||
| Reported EU Net Revenues at Constant Currency | 1.499.023 | 1,255,927 | 19.4% |
| In thousands of euros | 2024 | 2023 | 96 Var |
| Reported ROW Net Revenues | 1,626,455 | 1,437,089 | 13.2% |
| Variation due to Exchange Rate Effects | 28,202 | ||
| Reported ROW Net Revenues at Constant Currency | 1,654,657 | 1.437.089 | 15.1% |
◦
| 04:24 | 03:24 | 02:24 | 01:24 | 04'23 |
|---|---|---|---|---|
| 8.836 | 8,752 | 9,650 | 10.034 | |
| (ਰਵਰ) | (1,025) | (1,026) | (1,004) | |
| 676 | 1.017 | 2,757 | 1,745 | 1,023 |
| (111) | (109) | (111) | (107) | |
| (645) | (2,113) | (449) | (530) | |
| 8,046 | 8,128 | 8,262 | 9,811 | 9.416 |
| 9.491 (1.025) (117) (980) |
| In millions of euros except ratio. | LTM Q4'24 | LTM Q3'24 | LTM Q224 | LTM Q1'24 | FY 2023 |
|---|---|---|---|---|---|
| OPERATING RESULT (EBIT) | 1,192 | 1,075 | 1,005 | ਰਤਮ | 781 |
| Depreciation & Amortization | (439) | (443) | (444) | (441) | (458) |
| Reported EBITDA | 1,631 | 1,518 | 1,450 | 1,375 | 1,239 |
| IFRS 16 | (113) | (113) | (110) | (104) | (102) |
| Restructuring costs | 55 | 5/ | 34 | 24 | ਹਵਿਕ |
| Transaction costs | 49 | 59 | 65 | 59 | 48 |
| Cost savings, operating improvements and synergies on a "run rate" |
। ਦਰ | 146 | 136 | 131 | 134 |
| Other one-offs | (28) | (62) | (75) | (43) | (1) |
| Total adjustments | 122 | 87 | 50 | 66 | 232 |
| Adjusted EBITDA LTM as per Credit Agreement | 1,753 | 1,605 | 1,500 | 1,442 | 1,471 |
| Leverage Ratio as per Credit Agreeement | 4.6x | 5.1x | 5.5x | 6.8x | 6.4x |
| In thousand of euros | ||||||
|---|---|---|---|---|---|---|
| Q4 2024 | Q3 2024 | Q2 2024 | Q1 2024 | FY 2024 | Q4 2023 | |
| OPERATING RESULT (EBIT) | 371.859 | 317.034 | 299.321 | 203.802 | 1,192,016 | 255.252 |
| Depreciation & Amortization | (110,130) | (108,364) | (114,310) | (106,139) | (438,944) | (113,869) |
| Reported EBITDA | 481.990 | 425.398 | 413.631 | 309,941 | 1,630,960 | 369,122 |
| 96 Net revenue | 24.496 | 23.796 | 22.896 | 19,196 | 22.696 | 20.996 |
| Restructuring costs | 1.889 | 21,673 | 10.095 | 2,326 | 35,982 | 19,916 |
| Transaction costs | 9.306 | 7.882 | 16.145 | 15,318 | 48,650 | 19,590 |
| Impairments | 24,265 | 787 | 25,052 | 1,794 | ||
| Biotest Next Level Project | 7.340 | 5.113 | 4.922 | 16.798 | 34.173 | 33,100 |
| SRAAS One-off | (5,618) | (5.618) | ||||
| Other non-recurring items | 1.155 | 1.245 | 1.613 | 6.020 | 10,032 | |
| Total adjustments | 43.954 | 36.700 | 27.157 | 40.461 | 148.271 | 74.400 |
| Adjusted EBITDA | 525.944 | 462.098 | 440.788 | 350.402 | 1.779.232 | 443.522 |
| 96 Net revenue | 26.696 | 25.896 | 24.296 | 21.696 | 24.796 | 25.196 |
| In thousand of euros | 04'24 | 03'24 | Q2'24 | 01 24 | 04'23 |
|---|---|---|---|---|---|
| Property, Plant & Equipment additions ("CAPEX reportado") | 99.505 | 51.207 | 43.479 | 38.405 | 38.405 |
| Interest capitalized | 4.820 | 7513 | 7.583 | 7.799 | 7.799 |
| Total PP&E additions | 104,325 | 58,720 | 51.062 | 46.204 | 46.203 |
(Free translation from the original in Spanish. In the event of discrepancy, the Spanish-language version prevails)
At their meeting held on 25 February 2025, pursuant to legal requirements, the Directors of Grifols, S.A. authorized for issue the consolidated annual accounts and consolidated directors' report for the period from 1 January 2024 to 31 December 2024. The consolidated annual accounts comprise the documents that precede this certification.
| Thomas Glanzmann (signed) Chairman |
José Ignacio Abia Buenache (signed) Board Member |
Raimon Grifols Roura (signed) Board Member |
|---|---|---|
| Víctor Grifols Deu (signed) Board Member |
Albert Grifols Coma Cros (signed) Board Member |
Tomás Dagá Gelabert (signed) Board Member |
| Iñigo Sánchez-Asiaín Mardones (signed) Board Member |
Anne-Catherine Berner (signed) Board Member |
Enriqueta Felip Font (signed) Board Member |
| Pascal Ravery (signed) Board Member |
Montserrat Muñoz Abellana (signed) Board Member |
Susana González Rodríguez (signed) Board Member |
| Paul S. Herendeen (signed) Board Member |
Núria Martín Barnés (signed) Secretary to the Board |

| General | 3 |
|---|---|
| Understanding Grifols | 4 |
| Our stakeholders | 13 |
| Double materiality | 15 |
| About this report | 19 |
| Environment | 22 |
| Environmental management | 23 |
| EU Taxonomy | 28 |
| Climate Change | 37 |
| Pollution | 56 |
| Water resources | 61 |
| Biodiversity | 69 |
| Circular Economy | 71 |
| Social | 81 |
| Our people | 82 |
| Workers in the value chain | 128 |
| Plasma donors and comunities | 131 |
| Patients and healthcare professionals | 146 |
| Innovation at Grifols | 163 |
| Governance | 174 |
| Governance of a listed company | 175 |
| Conducta empresarial | 183 |
| Cybersecurity and data protection | 196 |
| Risk management and control | 199 |
| Taxation | 205 |
| Annexes | 209 |
| Indices of content according to regulations | 210 |
| Methodologies | 222 |
| Glossary and abbreviations | 225 |
| Independent Review Report | 228 |
Business model 4 Value chain 7 Sustainability strategy and approach 9
3
General basis for preparation of sustainability statements. scope and limitations
Governance, risk management and internal control on sustainability disclosures and statement on due diligence
3 2024 Non-Financial Information Statement and Sustainability reporting
General Environment Social Governance Annexes

19
20
Grifols is dedicated to enhancing the health and well-being of people around the world. Since 1909, we have been at the forefront of innovation, advancing plasma science and diagnostic solutions to contribute to social progress.
Enhance global health to help people live longer and healthier lives
Amplify our positive impact to advance our sustainable business model
Grifols Group ( henceforth "Grifols") is a global healthcare company dedicated to improving people's health through the innovation, development, production and commercialization of essential plasmaderived medicines, non-plasma therapies and diagnostic solutions.
Today, Grifols stands as a global leader in plasma therapies and transfusion medicine.
Grifols' business model includes four business units: Plasma Procurement and Biopharma1 , Diagnostic, Bio Supplies and Other. Each offers specific products and services, ensuring a diversified approach to healthcare, a positive impact on patients and optimal solutions for healthcare professionals.

Plasma procurement, production and commercialization of plasma and non-plasma solutions
85% over revenues (EUR 6,143 M)
BIO SUPPLIES
Leading-edge diagnostic solutions for blood and plasma analyses
High-quality biological products for non-therapeutic use
9% over revenues (EUR 645 M)
3% over revenues (EUR 216 M)
Specialty pharmaceuticals and hospital management solutions
3% over revenues (EUR 209 M)
Total income 2024 EUR 7,212 M
Grifols' business model places people at the heart of its operations, with a focus on patient health and the well-being of Plasma donors whose generosity make plasma-derived medicines possible. Grifols serves as the bridge between Plasma donors and patients.
In 2022, Grifols finalized its strategic investment in Biotest AG. Since then, both companies have collaborated closely to expand access to plasma therapies for the benefit of patients worldwide.
Plasma and non-plasma therapies
IMMUNOLOGY AND NEUROLOGY
Immunodeficiencies and autoimmune disorders
PULMONOLOGY
Alpha-1 antitrypsin deficiency
HEMATOLOGY
Hemophilia and other bleeding and clotting disorders
HEPATOLOGY AND INTENSIVE CARE
Hypovolemia and hypoalbuminemia in liver diseases, cardiac surgery, severe infection and other conditions Diagnostic solutions Transfusional and Clinical
IMMUNOLOGY AND NEUROLOGY
HEMATOLOGY
HEPATOLOGY ANDINTENSIVE CARE
INNOVATION


| Clayton Emeryville |
North Carolina Hub Research Triangle Park |
Hub California San Carlos |
U.S. 298 |
|---|---|---|---|
| Los Angeles | Los Angeles | Canada 3 | |
| San Diego | San Diego | ||
| Memphis | Emeryville | ||
| Montreal | |||
| Vista | |||
| Clayton | Emeryville | Memphis | |
| Los Angeles | Raleigh-Durham | Vista | |
| Montreal | San Diego |
Raleigh-Durham

| Barcelona | Germany 62 Hungary 19 |
Barcelona Bilbao |
Hub Europe Dublin |
Melbourne |
|---|---|---|---|---|
| Czech Republic 14 Austria 3 |
Dublin Düdingen Dreieich |
Barcelona Bilbao Zaragoza |
||
| Leipzig Murcia San Sebastián |
Düdingen Dreieich |
Melbourne | ||
| China | ||||
| Barcelona Dublin Dreieich |
Barcelona Düdingen |
Leipzig | Barcelona Murcia San Sebastián Bilbao |
The production of plasma-derived medicines, driven by the Plasma Procurement and Biopharma business units, lies at the core of Grifols' operations. These areas are further supported by the Diagnostic and Bio Supplies business units, which enhance and optimize the company's value chain.
Grifols stands out for its rigorous management of the value chain, grounded in ethical principles, quality and sustainability that exceed regulatory requirements. The company promotes a sustainable and responsible value chain, continuously incorporating due diligence policies and procedures.
This approach promotes managerial excellence and helps prevent or mitigate negative impacts, both real and potential, on human rights and the environment. In parallel, it also helps minimize risks and capitalize on surrounding opportunities.
To this end, Grifols integrates environmental, social and governance (ESG) principles throughout its value chain. The company is committed to ensuring the highest standards of quality and safety in its products and services, building trust and loyalty among patients, plasma donors and the healthcare community.
| Plasma donors | Plasma donation centers |
Production plants | |
|---|---|---|---|
| Description: Donors are an essential part of Grifols' value chain, specialized in plasma-derived medicines. Role: They provide the raw material |
Description: Grifols operates a broad network of plamsa donation centers. Role: They safely collect, process and store plasa in compliance with strict norms and |
Description: Grifols has state-of-the-art installations for the fractionation of plasma and purification of plasma proteins. Role: They transform plasma into specific |
|
| necessary to produce plasma-derived medicines. |
regulations. | medicines including immunoglobulins, albumins, alpha-1 and clotting factors. |
|
| Regulatory bodies | Research and development centers (R+D) |
Distributors and sales force |
|
| Description: Government organisms and internatinal agencies such as the FDA, EMA and other local authorities |
Description: Grifols invests in innovation through in-house R+D and its investees. |
Description: Companies and entities that distribute Grifols products globally. |
|
| Role: They guarantee processes and products comply with safety and quality norms. |
Role: They develop new therapies and diagnostic solutions, while improving existing processes. |
Role: They facilitate the delivery of products to hospitals and healthcare centers. |
|
| Logistics and transport |
End clients | Consumers and patients |
|
| Description: Companies in charge of transporting plasma and finished products under controled conditions. |
Description: Hospitals, healthcare centers, healthcare professionals and patients. |
Description: Patients who need specific plasma-derived therapies. |
|
| Role: They guarantee that products arrive on time and in optimal conditions. |
Role: They use specific treatments, especially in areas such as hemotology, immunology and intensive care, among others. |
Role: They are at the heart of Grifols' activity. |
More details on resource inputs (raw materials) in the value chain and resource outputs (end products): "Circular Economy" in the "Environment" chapter.
More details on supplier management and relations: "Governance" chapter
Melbourne
RoW
Melbourne
China



As a worldwide leader in plasma-derived medicines, Grifols centers its strategy on ensuring a sustainable plasma supply through an extensive global network of donation centers, while continually optimizing its production processes. Its diversified portfolio includes both plasma and non-plasma therapies, along with diagnostic and hospital solutions that complement its core business and extend its reach.
Grifols drives global growth through strategic acquisitions, market expansion and key alliances. Its unwavering commitment to innovation is evident in its continuous development of new therapies and advanced technologies, supported by high-potential subsidiaries such as Biotest AG, GigaGen Inc. and Alkahest Inc., among others. This innovative approach further reinforces its industry leadership.
At the same time, the company strives to fortify a robust financial strategy that promotes growth and maximizes shareholder value. With over 115 years of history and a legacy of four generations dedicated to serving society, Grifols continues to advance as a global benchmark in the healthcare sector.
Grifols is committed to sustainability, with a dual focus on economic growth and a staunch commitment to social and environmental responsibility. The company recognizes the inseparable connection between the environment and human health, understanding the impact of pollution, climate change, biodiversity loss, ecosystem degradation and other factors on living conditions and people's physical and mental well-being.
From Grifols' perspective, this integration not only promotes a more sustainable future but also enhances the organization's long-term value by reinforcing its resilience and adaptability in a dynamic global market.
In this regard, Grifols has made significant progress in recent years, while remaining focused on embedding sustainability across all its business functions and units through a holistic, cross-cutting approach. The progress achieved and commitments made in 2024 are detailed in this report.
| Plasma | Guarantee plasma supply and access to treatments Promote a diversified network of plasma centers and maximize their efficiency |
|---|---|
| Innovation | Prioritize critical innovation projects Focus on differentiated products through in-house and investee-led initiatives Integrate innovation and digital transformation projects that streamline processes and add value to the business model |
| Plasma donors and patients | Greater commitment to patients, healthcare professionals and plasma donors |
| Talent | Foster leadership Promote a culture based on talent recognition and continuous development Advocate and promote diversity, inclusion and equal opportunity Promote employee health and well-being |
| Financial performance | Reduce debt Financial discipline and cost control Sustainable growth |
| New business models and expansion |
Promote public-private collaborations to increase countries' self-sufficiency in plasma-derived medicines Establish strategic alliances in high-potential markets |
| Sustainability | Continue to build an organization-wide culture of sustainability Maintain a robust sustainability strategy and roadmap Increase the integration of ESG analyses and evaluations in decision-making frameworks |
Grifols' approach to integrating sustainability is outlined in the Sustainability Policy and Sustainability Master Plan, which forms part of the company's Strategic Plan and aligns with the United Nations Sustainable Development Goals (SDGs).
In 2024, the company began updating its Sustainability Master Plan for 2025-2027, considering the impacts, risks and opportunities identified through the double materiality analysis; new ESG-related regulatory
requirements; emerging market and societal expectations concerning global sustainability; and its corporate strategy.
With this revision, the company will enhance its ability to anticipate emerging risks, comply with regulatory and societal expectations, and solidify its role as a sustainability leader to ensure a positive long-term impact.
Overview of corporate policies: "Governance" chapter.

Our Aim: employees feel they are part of a company that promotes diversity, continuous development, equal opportunities, gender equality
and that strives to improve well-being at the workplace

MAIN PILLARS


local communities
Our Aim: solid community where every donor feels valued for its commitment and understands its impact beyond compensation, and every patient receives the treatment it requires
Our Aim: advance towards the common good of having healthy places to live, work and play, by raising awareness on the need to protect the planet
Our Aim: healthier and wealthier society, by positively contributing to social progress, supporting organizations and actively participating in

ENCOURAGING ETHICAL PRACTICES FOSTERING INNOVATION

Our Aim: placing human rights at the core of our practices and having the highest ethical standards integrated throughout the supply chain
Our Aim: scientific progress addressing the needs of our patients, lead by our pioneering spirit and protecting the rights, safety and well-being of clinical trial participants
In 2021, as part of its sustainability strategy, Grifols established 30 corporate goals aligned with the SDGs: the Grifols 2030 Agenda. In 2022, the company once again ratified its commitments, setting intermediate targets to be achieved by 2024, as detailed below:
| Environmental responsibility | Intermediate milestones 2024 | |
|---|---|---|
| 55% decline in GHG emissions per unit of production | -15% | 4 |
| 15% increase in energy efficiency per unit of production | +5% | 4 |
| 100% electricity consumed from renewable sources | 27% | 4 |
| Promote decarbonization in business travel and work commutes | Same target 2030 | 4 |
| Increase circular economy measures at each stage of the operational life cycle | Same target 2030 | 4 |
| Protect biodiversity in the company's natural areas to capture CO2 | Same target 2030 | 4 |
| Our people | ||
| Impart 100 hours of training hours/year/person | Same target 2030 | 4 |
| Deliver annual training to 70-80% of the workforce | Same target 2030 | 4 |
| Increase percentage of women in Senior Manager roles to 50% | 41% | 4 |
| Increase percentage of people with disabilities to 3-5% of total employee pool | Same target 2030 | 4 |
| Ensure women comprise 50% of interviews for managerial positions | 45% | 4 |
| Maintain employee turnover rate below industry average* | Same target 2030 | 4 |
| Achieve 70% overall employee engagement rate per department | 63% | 4 |
| 75% increase in installations certified as healthy workplaces | 54% | NA |
| 15% decrease in LTIFR (lost time injury frequency rate) | 5.3% | 4 |
| 75% of installations with ISO 45001 certification | 54% | In process |
| Commitment to plasma donors and patients | ||
| Achieve EUR18 million per year in donations to support patient programs | 13 M EUR/year | In process |
| Increase donations of clotting factors to 240 million IU | 90M UI | 4 |
| Achieve 90% approval among donors for positive customer service (good or excellent rating) | Same target 2030 | NA |
| Attain 80% referral rate from active donors | Same target 2030 | 4 |
| Increase ratings via the Donor Hub by 45% | Same target 2030 | NA |
| Social impact | ||
| Increase the number of social outreach initiatives and investments by 50% | 35%+ (initiatives) 13%+ (social investment) |
In process |
| Allocation of 25% of social initiatives for STEM scholarships for women | 20% | In process |
| Reach USD1 million in donations of products and medicines for emergency relief efforts | 750 k USD | 4 |
| Increase funds for José Antonio Grifols i Lucas Foundation by 10% | 10% | 4 |
| Increase by 10% the amount allocated to bioethics grants and by 20% number of activities developed by Víctor Grifols i Lucas Foundation |
10% | 4 |
| Ethical commitment 2030 | ||
| Implement ESG criteria among suppliers up to 60-80% of total spending volume | 25% | 4 |
| Maintain Biopharma claims ratio in ≤ 1/50,000 | Same target 2030 | 4 |
| Maintain <1 critical deficiencies identified by external audits (health regulatory authorities) | Same target 2030 | 4 |
| Innovation | ||
| Promote in-house and external innovation in core therapeutic areas | Achieve 80%+ of milestones defined in key innovation projects |
4 |
| Allocate at least 75% of R&D investment to new products and market development |
4 |
*Not including employees at Grifols' plasma donation centers.
IU= International Units
In progress: Grifols is working to align with that objective.

Grifols was ranked the number one biotechnology company in the 2024 S&P Dow Jones Best-in-Class Indices (previously DJSI), earning its highest ever score of 70, seven more than in 2023. The company has been distinguished on the Dow Jones Best-in-Class World Index (previously DJSI World) and the Dow Jones Best-in-Class Europe Index (previously DJSI Europe) for the fourth and fifth consecutive years, respectively.

Grifols was awarded the EcoVadis Gold Medal for the second consecutive year. With a score of 77 points, the company is an established leader in this field, ranking in the top 5%.

In 2024, Grifols scored an B rating from the Carbon Disclosure Project (CDP) Climate Change

Grifols earned the Prime badge in the ISS corporate ESG rating, positioning it as an industry leader its peer group.

Grifols is among the highest-rated companies by Sustainalytics, with a low ESG risk rating.

Grifols was listed on the FTSE4Good in 2024 for another year running in recognition of its solid ESG practices.

In 2024, Grifols received a BBB score from MSCI ESG Ratings.

Grifols' short-term objectives to reduce its carbon emissions were approved by Science Based Targets (SBTi).

Grifols continually integrates the interests and views of its stakeholders into its corporate strategy and business model, recognizing the crucial role they play in its long-term success.
To this end, Grifols fosters trust-based relationships and effective dialogue, enabling it to identify the most relevant stakeholder issues and emerging sustainability trends.
More information on how Grifols addresses the interests and views of its stakeholders: "Double Materiality" section.

● We foster collaboration with our stakeholder groups to advance our purpose and progress on achieving Grifols 2030 Agenda objectives.

● We encourage the participation and involvement of our stakeholders by offering platforms for dialogue and forums that foster active listening.

● We routinely review stakeholder relationship mechanisms to ensure they respond as efficiently as possible to their current needs.
● We assure transparency in stakeholder relations and financial and non-financial disclosures by sharing truthful, relevant, complete, comparable, clear, up-todate and useful information.
The primary reporting platforms on Grifols activities include the Integrated Annual Report; quarterly earnings presentations; specific reports, primarily those generated to comply with legal requirements in the U.S., where Grifols securities are also traded (20F); publications on global and local websites; and social media outlets (LinkedIn).

● Grifols provides information to its stakeholders in a clear, concise and ethical manner.
Grifols has identified and implemented appropriate communication channels to ensure open dialogue with stakeholders, stay aligned to their needs and expectations, and encourage interaction. The following table provides an overview of the company's communication outlets for its various stakeholder groups:
Grifols has open lines of communication through electronic and phonebased channels. The company contacts patient associations every month to discuss topics of interest and provide updates on its activity. In addition, it occasionally organizes meetings and visits to Grifols' corporate headquarters, production facilities and museums.
Grifols informs plasma donors via its website, educational videos and surveys to discern their level of satisfaction with the company and identify areas for improvement.
Grifols engages with customers (public and private sector; wholesalers, distributors, group purchasing organizations (GPOs), blood banks, hospitals, and healthcare institutions (public health/social security systems) to provide clear and comprehensive information all of its products.
Grifols utilizes formal channels to communicate with regulators such as the FDA, EMA, AEMPS, and other regulatory authorities on matters related to clinical trials, authorizations for plasma donation centers, validation of production facilities and other clearances for the sale of plasma-derived therapeutic treatments, including new medicines and indications.
Formal communication channels are utilized during certification, evaluation and auditing processes, while informal channels are used for day-to-day communication.
Grifols collaborates with various NGOs through its foundations and directly by supporting diverse community initiatives in its markets of operation.
Grifols maintains transparent communication with journalists and other media representatives. The company issues press releases to announce significant events, including quarterly and annual results, and hosts at least one meeting per year in conjunction with its General Shareholders' Meeting.
Collaboration with research partners and scientific institutions is crucial to Grifols' continuous innovation in both products and processes. The company's engagement with the scientific community includes participation in R&D projects, strategic investments and active involvement in industry associations.
Grifols discloses relevant information in accordance with the legal requirements set by regulators and the securities markets on which it is listed (CNMV, SEC, NASDAQ, ISE), using the appropriate channels for each entity.
The company also engages with shareholders, investors, analysts and other stakeholders by organizing and attending meetings, including the General Shareholders' Meeting, business gatherings, analyst calls and roadshows. Grifols publishes an annual report, quarterly reports and press releases on its corporate website, which are accessible to interested parties through subscriptions to distribution lists, when necessary.
Grifols holds an annual meeting exclusively for analysts and investors featuring more in-depth presentations. The company also offers a dedicated email channel for the investment community to send feedback and queries.
Grifols maintains an employee intranet that is continuously updated, along with viewing screens in several facilities displaying general interest information. The company also publishes an employee magazine and organizes semi-annual meetings, while leveraging other communication channels and informal outlets.
The Human Resources team periodically conducts a climate survey to gain deeper insights into workforce needs. It also has dedicated email channels for both human-resource queries and sustainability-related issues.
The company establishes relationships with institutional bodies, trade groups and other professional organizations through both formal and informal channels. These interactions include the organization of forums, congresses and other business-related meetings.
Grifols provides more information on its communication with key stakeholders at the beginning of each section of its Non-Financial Information Statement and Sustainability reporting, in accordance with each stakeholder group addressed in each ESRS.
Aware of its far-reaching impact on the environment, Grifols places great emphasis on responsible business conduct. To this end, sustainability risk analysis has become a core component of its global risk management. Environmental, social and governance factors are intricately linked to traditional business risks and can significantly influence the company's development. Grifols has incorporated ESG risks into its global risk map1 in reflection of their strategic relevance to the company.
As part of this commitment, Grifols conducted a double materiality analysis for the second consecutive year. In alignment with the new European Corporate Sustainability Reporting Directive (CSRD), this approach enables Grifols to identify the significant impacts it has on the environment and society, as well as the external risks and opportunities that could materially affect its financial performance.

Five-step methodology

A comprehensive analysis of Grifols' global business model is crucial to effectively identify and assess its impacts, risks, and opportunities (IROs). In the initial phase, the company's activities–both internal and across the value chain (upstream and downstream)–were thoroughly mapped. Simultaneously, stakeholders who may be impacted by or have influence on the company's operations were identified. This information is essential for developing a robust double materiality analysis.
For more information on Grifols' business model and value chain, see the section Understanding Grifols
The objective of this phase is to determine the impacts that Grifols' activities generate or could generate on the environment and society, both directly and indirectly (across its value chain). Additionally, it identifies the risks and opportunities in the external environment that could affect the company from a financial perspective, taking into account the following information:
More information: "Stakeholders" section.
The materiality of the previously identified IROs is assessed in this phase in line with the criteria defined in ESRS 1-General Requirements of the CSRD.
The indicators applied differ depending on whether the assessment focuses on impacts or on risks and opportunities. In either case, the values for each indicator–such as probability or severity–are determined by considering both the aforementioned internal and external information.
The risk assessment is carried out using the following indicators as a base:
● The likelihood of the impact's occurrence (where 10% is very unlikely and 90% is very likely).
The assessment does not consider current impacts as they are already occurring. In accordance with best practices, this indicator is not evaluated for human rights-related impacts in order to give greater weight to severity.
The assessment of risks and opportunities is carried out using the ERM2 Risk Assessment Model and includes:
Potential magnitude of the financial effects of each risk and opportunity (where 1 is very little and 5 is high). The analysis of the financial impact was conducted considering qualitative criteria and factors.
Enterprise Risk Management
More information on risk management and control: "Governance" chapter.,
For Grifols, incorporating the interests and views of its stakeholders into its business strategy is essential. To this end, their integration in its identification and assessment processes is also key. Stakeholder interests and views are considered from three perspectives:
Specific actions: In addition to maintaining continuous dialogue, Grifols spearheaded a series of initiatives in 2024 to gain a deeper understanding of its stakeholders' needs and interests. These included:
Consultation of documentation from independent experts: Stakeholder viewpoints were integrated by analyzing reports and communications from a range of representative organizations, including plasma donors, patients, employees, public health systems, foundations, NGOs and local communities. The following organizations and documents were reviewed:
The final results of the analysis were presented and approved by the Sustainability Committee, Appointments and Remunerations Committee and Grifols Board of Directors of Grifols.
Each CSRD (Corporate Sustainability Reporting Directive) topic and subtopic encompasses the impacts, risks, and opportunities that are material to Grifols' activity. These material topics and sub-topics can be identified based on the IROs that define each area.
Information on the material IROs of each sub-topic: consult specific chapter

| Topic | Patients and healthcare professionals (S4) | Climate change (E1) | Plasma donors and donor communities (S3) |
|---|---|---|---|
| Sub-topics | Impacts related to information (29) Personal safety (30) Social inclusion of consumers (31) |
Adaptation to climate change (1) Mitigation of climate change (2) Energy (3) |
Communities' economic, social and cultural rights |
| Material IROs* | ● Responsible and transparent business conduct (I+) (SP) ● Improvement in patients' well-being (I+) (SP) ● Quality and safety of products and services (I-) (R) ● Intensification of health policies and other regulations (R) ● Access to treatments and diagnostics (I+-) (R) ● More sustainable healthcare systems (I+) (OO) |
● Increase in extreme weather events (R) ● Contribution to climate change through GHG emissions from scopes 1, 2, and 3 (I-) (OO) (SP) ● Non-compliance with climate goals or legal requirements (R) ● Non-renewable energy consumption (I+-) (OO) Insufficient energy supply (R) |
● Health and well-being of plasma donors and their communities (I+-) (OO) (SP) (R) ● Contribution to communities' local and social development (I+) (OO) (SP) |
| Why is it material? |
Grifols, through its products, has a profound impact on patients' lives. The company's ability to provide safe, effective and accessible treatments is crucial to public health. |
Climate change presents a challenge with far reaching implications for Grifols. At the same time, the company can potentially make a significant contribution to mitigating climate change mitigation through improvements in operational efficiency, the adoption of renewable energy, and the development of sustainable products and processes. |
Grifols operates in a complex and dynamic environment characterized by significant risks and opportunities linked to the availability of plasma and the well-being of donor communities. |
| Impact on the company |
Grifols' commitment to patient health and the satisfaction of healthcare professionals is essential for its long-term growth and sustainability. Product quality and safety related risks, as well as those arising from potential regulatory changes, must be carefully managed to mitigate any potential financial impacts. |
Grifols can contribute to a more sustainable future by integrating sustainability into its core business strategy. Nevertheless, climate change also presents significant risks to Grifols' operations. Extreme weather events and emissions-related regulatory changes may impact its financial performance and operational resilience. |
Grifols has the potential to generate significant positive impacts by creating jobs and contributing to public health through its life-saving therapies. At the same time, plasma shortages and risks to plasma donors' health pose threats to the company's operations. By proactively addressing these challenges, Grifols can help ensure the long term sustainability of its business. |
| Business strategy | The management of the impacts, risks and opportunities of Grifols' activities on patients and healthcare professionals is outlined in "Patients and Healthcare Professionals." This section includes a description of the policies and actions implemented to promote patient well being, ensure access to treatments and other initiatives undertaken in this regard. |
The management of the impacts, risks and opportunities related to climate change is outlined in the "Climate Change" section, which includes a description of the policies and actions established to address this topic.** |
The management of the impacts, risks and opportunities related to this topic is outlined in the "Donors and Donor Communities" section, which includes a description of the policies and actions established to ensure the health of plasma donors and advance community development. |
| Integration in risk management |
The risks identified regarding this material topic are fully integrated into the company's ESG risk management system. For more details, see "Patients and Healthcare Professionals" section. |
The risks relating to climate change are fully integrated into the company's risk management system. The identified risks and the actions designed for their mitigation are developed further in the "Climate Change" section.** |
The risks identified regarding this material topic are fully integrated into the company's ESG risk management system. These risks are further developed in the "Donors and Donor Communities" section. |
| Performance metric (2030 objective) |
● Biopharma claims ratio (maintain below 1/50,000) ● Number of critical deficiencies identified by external authorities (maintain below 1) ● Financial donations to support patient programs (EUR 18M/year) ● Clotting factor donations through the FMH agreement (240M IU) ● Product and medicine donations for emergency relief through Direct Relief (USD 1M)*** |
● Absolute scope 1 and 2 GHG emissions (42% reduction compared to 2022. Science-based target)* ● Absolute scope 3 GHG emissions (25% reduction compared to 2022. Science-based target) ● GHG scope 1 and 2 emissions per unit of production (55% reduction compared to 2018) ● Energy efficiency per unit of production (15% increase compared to 2018) ● Electricity consumption from renewable sources (100%) These objectives and targets are also incorporated in Grifols' three-year corporate environmental program.**** |
● Number of social initiatives and their investment (50% increase compared to 2020 and 2021, respectively) ● Percentage of social initiatives dedicated to STEM scholarships for women (25%) ● Resources allocated to the José Antonio Grifols Lucas Foundation (10% increase compared to 2020) ● Resources dedicated to scholarships and activities carried out by the Víctor Grífols i Lucas Foundation (10% and 20% increase, respectively, compared to 2020) |
| Executive | Among other factors, executive variable compensation is subject to financial and non-financial metrics and parameters, including a specific metric linked to the |
|---|---|
| variable | achievement of ESG objectives. In 2024, 10% of the variable compensation is tied to ESG factors, with 25% related to environmental, 40% to social and 35% to |
| compensation | governance factors.** |
*More information: See "Impacts, risks and opportunities" in the sections dedicated to each material issue.
**The impact of climate change on Grifols and its management is specifically addressed in the "Risk and Opportunities Management Related to Climate Change" report.
***Objectives integrated in Grifols 2030 Agenda. For more information on its progress and milestones, see "Grifols 2030 Agenda" in "Understanding Grifols."
****Objectives approved by the SBTi initiative. For more information, consult the section "Objectives to reduce emissions approved by the SBTi in the "Environment" chapter.
*****More information: see "Climate change mitigation under the 2023-2026 Environmental Program" in "Environment".
****** For more information, please refer to the Board of directors remuneration policy, Annual Corporate Governance Report and Directors' Remuneration Report in www.grifols.com; also see "ESG criteria in long-term compensation" section of this report.

Bases for the preparation of the Non-Financial Information Statement and Sustainability reporting
This report has been prepared in accordance with the current legislation for a Non-Financial Information Statement (see Annex - Index of the content required by Law 11/2018, of December 28).
The Board of Directors of Grifols, S.A. has formulated the Non-Financial Information Statement and Sustainability reporting for the 2024 financial year as a separate document and integral part of the Consolidated Management Report and as a separate document from the consolidated annual accounts.
This report includes the impact of the group's activity with respect to environmental and social issues; respect for human rights; initiatives relating to the fight against corruption and bribery; and those relating to personnel, including the measures, if any, adopted to favor the principle of equal treatment and opportunities between women and men, nondiscrimination and inclusion of people with disabilities and accessibility.
The company has considered the requirements of Directive 2022/2464/ EU (CSRD1 ), taking as a reference the set of standards, principles, and criteria related to sustainability information established in the European Sustainability Reporting Standards (ESRS) and other requirements applicable to the entity originating from Spanish legislation and directly applicable European regulations, including the requirements on Taxonomy contemplated in Article 8 of Regulation (EU) 2020/852 on taxonomy. (See Annex - Index of disclosure requirements in ESRS covered by the Sustainability statement (ESRS 2 – IRO-2)).
Grifols followed a double materiality approach in this report, analyzing the materiality of the requirements of Law 11/2018, considering the opinion of its main stakeholders and adhering to the new CSRD requirements.
This report covers the period from January 1 to December 31, 2024, corresponding to Grifols' fiscal year.
For the purposes of this report, Grifols S.A. and all its subsidiaries are considered as "Grifols2 ". The reported information includes all dependent companies with a stake greater than 51% or under control according to the IFRS definition as reflected in the Consolidated Financial Statements.
Biotek America LLC, a joint operation between Grifols and Immunotek GH LLC, has not been included in the scope of this report due to the Group's lack of sufficient non-financial and sustainability information regarding this entity. As of December 31, 2024, this company operates 14 plasma centers3 . The Group will take the necessary steps to include information on the locations (14 plasma centers) of Biotek America LLC in the report to be prepared following its planned acquisition during 2025 (see Notes 10 and 34 of the consolidated financial statements).
In relation to the Non-controlled entities by Grifols, S.A. - Grifols Egypt for Plasma Derivatives (S.A.E.), Medcom Advance, S.A., BioDarou PLC and Shanghai RAAS Blood Products Co. Ltd.– have been considered in the calculation of the environmental footprint.
Except as indicated above, this report covers Grifols' main business units4 : Plasma Procurement and Biopharma5 , Diagnostic, Bio Supplies and Others, which together account for 100% of the group's turnover. These business units integrate all the key operations of the group's value chain, from procurement (including plasma collection) and manufacturing, to affiliates.
Regarding value chain operations for which information was not available and could not be estimated, Grifols has applied the three-year moratorium provided for in the Transitional Provision of Article 5 of the CSRD Directive, which allows companies a period of adaptation before fully implementing the new reporting requirements.
This regulation complements Directive 2013/34/EU regarding the disclosure requirements on sustainability information.
A list of Grifols' subsidiaries can be found in Appendix I of the Consolidated Annual Accounts for the fiscal year ended December 31, 2024.
of plasma centers owned by the Group as of December 31, 2024.
For more details on Grifols' main business units, please refer to the section "Understanding Grifols".
The Plasma Procurement and Biopharma business unit corresponds to the Biopharma segment as described in Note 5 of the consolidated financial statements.
3. The 14 plasma centers of Biotek America LLC represent 3.39% of the total number
Grifols believes that this report provides a fair and balanced view of the company's economic, environmental, and social performance. While there are certain exceptions to the scope, as detailed above, these do not materially impact the consolidated indicators and therefore should not affect the reader's assessment of the company's performance.
For a comprehensive understanding of the information in this report, please consider the following additional points.
The data provided in this section represents Grifols' total production and commercial activities with the exception of commercial subsidiaries with fewer than 10 employees.
Since most of Grifols' manufacturing facilities are located in the United States and Spain, the environmental information included in this section is classified by division and region as U.S., Spain and rest of the world (RoW).
Grifols included figures for the last two years classified by gender (female, male, non-binary and not declared), age and region (U.S., Europe and RoW) in all cases where historical figures were available. Europe includes Austria, Czech Republic, France, Germany, Ireland, Italy, Poland, Portugal, Spain, Sweden, Switzerland and the United Kingdom.
The scope of the indicators related to remuneration includes the workforce in the United States, Spain, Germany and Ireland.
The data provided by Grifols regarding training hours represents 98,1% of the total workforce as of December 31, 2024. It includes all companies within the group except for Plasmavita Healthcare, Alkahest Inc, GigaGen Inc, Grifols Inn and New Technologies, and Haema Plasma Kft.
Indicators for absenteeism, people with disabilities and accident rates are limited to data from the United States, Spain, Ireland and Germany.
Regarding comparability, for the data reported on the Biotest group, the performance data of this company, particularly regarding human resources and the environment, is presented in separate tables to allow for comparability with previous years' data. Within the tables titled "Grifols", the following considerations should be taken into account: (1) the 2023 tables include the wholly-owned subsidiaries acquired in 2023: Biotest France SAS, Biotest UK Ltd., Biotest Italy S.r.l., Biotest Farmaceutica Ltda., and Biotest Medical S.L.U. (2) In 2024, the aforementioned companies, except for Biotest UK Ltd., have merged with other Grifols companies. Biotest AG annually publishes a set of management approaches and key policies on its corporate website.
Additionally, in the sections where historical data appear, figures for the last three fiscal years (2022-2024) have been included where available. The historical data presented in this report have not been recalculated to adjust for changes in perimeter that have occurred in each fiscal year or the application of the CSRD framework.
Grifols' sustainability governance is led by its Board of Directors. The company's Sustainability Committee, established by the Board, ensures adherence to principles and commitments related to environmental, social and governance responsibilities.
The governance processes, controls and procedures established by Grifols to manage, oversee and monitor sustainability matters are outlined in the "Governance" chapter. These include:
Grifols manages the risks and internal controls related to sustainability information disclosure through a comprehensive approach, with an emphasis on transparency, quality, reliability and alignment with internationally recognized standards.
In 2022, Grifols introduced a systematized reporting tool that has significantly enhanced the methodological rigor in the collection, support and validation of data.
The structure and content of the sustainability report, which includes the Statement of Non-Financial Information and consolidated sustainability information, are reviewed and approved by the Sustainability Committee, the Appointments and Remunerations Committee and the Board of Directors.
In terms of environmental reporting, Grifols has a standard operating procedure (SOP) which establishes the systematic approach to data collection, in which each user has a defined role: contributors provide the data, approvers validate it and administrators manage the system. In addition, internal audits are carried out to monitor the correct implementation of the process, which applies to all Grifols companies worldwide with more than 10 employees in offices, or where the company has more than a 50% shareholding. This procedure has been optimized with the implementation of software designed to collect and manage data in an efficient and structured manner. This system enables the preparation of the 2024 Non-Financial Information Statement and Sustainability reporting, as well as other internal and external reports.
In 2025, Grifols is developing its Global Reporting Manual, with the aim of standardizing and improving the reporting process for non-financial and sustainability information. This manual will provide clear guidelines to ensure transparency and consistency in the disclosure of environmental, social and governance (ESG) data.
| Core elements of due diligence | Section in the sustainability statement | |
|---|---|---|
| a) Embedding due diligence in governance, strategy and business model | General Information and Governance | |
| b) Engaging with affected stakeholders in all key steps of the due diligence | General Information, Environment, Social and Governance | |
| c) Identifying and assessing adverse impacts | General Information | |
| d) Taking actions to address those adverse impacts | General Information, Environment, Social and Governance | |
| e) Tracking the effectiveness of these offorts and communicating | General Information, Environment, Social and Governance |
| CONTENIDOS | |
|---|---|
| Environmental management | 23 |
| A cross-cutting and comprehensive approach | 23 |
| The internal regulatory framework - key policies | 24 |
| Certified Environment Management System | 24 |
| Environmental governance | 25 |
| Resources allocated to environmental management | 26 |
| Key performance indicators of environmental management | 27 |
| EU Taxonomy | 28 |
| Context and main conclusions | 28 |
| Taxonomy Framework | 29 |
| EU Taxonomy Key performance indicators | 31 |
| Climate Change - ESRS E1 | 37 |
| Impacts, risks and opportunities | 37 |
| Climate Change adaptation | 41 |
| Climate Change mitigation | 41 |
| Energy consumption and energy mix | 45 |
| Key performance indicators of Climate Change | 48 |
| Pollution - ESRS E2 | 56 |
| Impacts, risks and opportunities | 56 |
| Grifols' comprehensive approach to pollution management | 57 |
| Water pollution | 58 |
| Wastewater and discharge management | 59 |
| Key performance indicators of Pollution | 59 |
| Water resources - ESRS E3 | 61 |
| Impacts, risks and opportunities | 61 |
| Water is an essential resource for Grifols | 62 |
| Water withdrawal and consumption | 63 |
| Key performance indicators of water | 64 |
| Biodiversity - ESRS E4 | 69 |
| Grifols' biodiversity management | 69 |
| Biodiversity protection and conservation programs | 70 |
| Circular Economy - ESRS E5 | 71 |
| Impacts, risks and opportunities | 71 |
| Resource inflows: raw material consumption | 74 |
| Resource outflows | 75 |
| Waste management | 76 |
| Key performance indicators of Circular Economy | 77 |

General Environment Social Governance Annexes Environmental
management
Grifols' environmental management framework is focused on climate change, pollution, water resources, biodiversity and the circular economy. The company takes a holistic, integrated approach centered on eco-efficiency and prevention, regulatory compliance and proactive planning for both short- and long-term sustainability. This strategy is reinforced by a staunch commitment to environmental awareness and transparent communication. To support effective implementation, Grifols established an internal regulatory framework and an ISO 14001-certified environmental management system, applied across its production facilities.
● Implementation of legislative monitoring systems and regular compliance reviews in certified companies.

Grifols implements an ISO 14001-certified environmental management system for its main production facilities to identify and comply with all applicable environmental legislation; recognize the environmental impacts of its processes and products; implement necessary prevention and corrective measures; and establish objectives to boost its environmental performance. This standardized global system includes the corporate environmental manual, which offers an organization-wide framework for Grifols' environmental management.
All certified companies and those in the process of certification have an environmental committee led by their respective senior management team. This is the highest decision-making body responsible for defining environmental guidelines, ensuring implementation and maintenance of the Environment Management System, including allocating human and financial resources.
By the end of 2024, 73% of Grifols' total production – excluding Biotest was manufactured in ISO 14001-certified plants, and 70% of production workers operate in certified facilities.
Grifols prioritized the certification process of its largest production plants and is progressively certifying smaller facilities or those with a lower environmental impact. All certified plants undergo audits by the independent certification body TÜV Rheinland. Additionally, the company ensures its buildings and facilities are sustainably designed. In 2024, it continued to work toward LEED (Leadership in Energy and Environmental Design) certification for its new production facilities in Montreal, Canada. LEED is the world's largest scale green building rating system.
In 2024 Grifols was awarded a B-rating by the Carbon Disclosure Project Climate Change. The world's leading environmental disclosure platform, CDP annually assesses corporate climate strategies and performance. In line with its commitment to transparency with stakeholders, Grifols also participated in the CDP Water Report in 2024.
| MANAGEMENT | SUSTAINABLY DESIGNED AND ECO-EFFICIENT FACILITIES | ||||
|---|---|---|---|---|---|
| ISO 14001 | ISO 50001 | LEED CERTIFICATION* | GREEN GLOBES** | ZERO WASTE TO LANDFILL*** |
|
| SPAIN | All manufacturing, engineering, logistics and commercial companies |
Corporate headquarters in Barcelona |
|||
| USA | Biopharma facilities in Clayton (NC), Offices in Raleigh (NC), Diagnostic facilities in Emeryville (CA) |
Clayton (NC) office building Clayton (NC) raw materials warehouse |
Clayton (NC) Purification and filling plant Clayton (NC) fractionation plant |
Clayton (NC) production plant |
|
| CANADA | Fractionation plant and albumin New Montreal production plant (under construction to meet LEED requirements) |
||||
| BIOTEST | Dreieich (Germany) production facilities |
* Leadership in Energy and Environmental Design.
** Green Globes certified by the Green Building Initiative.
*** Zero Waste to Landfill, awarded by Underwriters Laboratories (UL).
Grifols' Board of Directors establishes a range of commitments to minimize environmental and climate risks and oversees their management, in addition to approving the Corporate Risk Policy, Sustainability Policy and other policies related to the environment, climate action, energy and biodiversity. Given its strategic importance, the Environmental Policy is signed by Grifols' CEO.
The Executive Committee regularly monitors Grifols' environmental performance and public reporting, including key climate-change indicators and actions, as well as financial risk and impact assessments associated with climate change.
The Sustainability Committee, Sustainability Steering Committee and Environment Committee drive and direct the implementation of the environmental objectives defined in Grifols' Sustainability Master Plan and environmental programs.
The Chief Industrial Services Officer (CISO), a member of the Executive Committee and Environment Committee, reports regularly to the CEO on the status of Grifols' environmental performance. The CISO also approves the Energy Policy, environmental program and allocation of economic and human resources to meet established environmental objectives.
With regard to remuneration policies and performance indicators, the Energy Manager receives incentives tied to the increase in renewable energy procurement through Power Purchase Agreements (PPAs).
Finally, the Corporate Risk Committee, which reports to the Board of Directors, develops and oversees the risk management model, ensuring an integrated approach to managing environmental risks and promoting sustainable business practices.

Grifols' robust governance framework oversees the management of environmental impacts, risks and opportunities.
At Grifols, the control, prevention and management of environmental risks is articulated through a global strategy. All of the company's ISO 14001-certified facilities operate under an environmental management system to minimize and mitigate environmental risks, including those derived from its operations (anthropogenic activity) and those produced by natural events (natural), such as extreme weather and climate-related phenomena.
Each facility has site-specific self-protection plans that define the necessary actions in the event of an environmental emergency and establish the designated teams responsible for their implementation.
Relevant training is provided for all those involved in environmental risk management in accordance with Grifols' continuous development plan.
Grifols' civil liability insurance policy covers accidental environmental pollution, defined as the disturbance to the natural state of the air, water, soil, flora or fauna (or any other situation classified as environmental pollution under applicable legislation) caused by emissions from its facilities as a result of single, sudden and unforeseen events. Grifols' liability extends to all its companies, production facilities and offices in all its regions of operation.
In 2024, Grifols no environmental-related financial penalties were issued in relation to adverse environmental impact.



Grifols allocated significant resources to environmental activities as part of its commitment to progressively advance on its 2023-2026 Corporate Environmental Program objectives.
In 2024, the total resources allocated to mitigating its environmental impact increased by 35% compared to 2023. Investments more than doubled, following a year of financial restraint, while operating expenses remained stable.
For more information on resources allocated to environmental activities, see the tables at the end of this section
| ENVIRONMENTAL EXPENSES | |||
|---|---|---|---|
| In thousands of euros | 2024 | 2023 | 2022 |
| Waste management | 20,362.00 | 21,290.00 | 17,544.51 |
| Water cycle | 7,918.45 | 6,660.11 | 7,893.98 |
| Reducing atmospheric emissions and energy | 60.09 | 84.00 | 57.69 |
| Others | 0.00 | 0.00 | 290.63 |
| Total | 28,340.54 | 28,034.11 | 25,786.81 |
| ENVIRONMENTAL EXPENSES - BIOTEST | ||||
|---|---|---|---|---|
| In thousands of euros | 2024 | 2023 | 2022 | |
| Water cycle | 0.00 | 1,594.00 | 0.00 | |
| Reducing atmospheric emissions and energy | 287.08 | 0.00 | 795.30 | |
| Total | 287.08 | 1,594.00 | 795.30 |
| ENVIRONMENTAL INVESTMENTS | |||
|---|---|---|---|
| In thousands of euros | 2024 | 2023 | 2022 |
| Waste management | 262.57 | 427.11 | 2,275.40 |
| Water cycle | 6,246.45 | 518.46 | 1,263.40 |
| Reducing atmospheric emissions and energy | 6,157.45 | 2,575.37 | 1,502.60 |
| Others | 3,149.16 | 1,253.39 | 3,331.00 |
| Total | 15,815.63 | 4,774.33 | 8,372.40 |
| ENVIRONMENTAL INVESTMENTS - BIOTEST | |||
|---|---|---|---|
| In thousands of euros | 2024 | 2023 | 2022 |
| Water cycle | 0.00 | 0.00 | 0.00 |
| Reducing atmospheric emissions and | |||
| energy | 293.00 | 1,000.00 | 0.00 |
| Total | 293.00 | 4,774.33 | 0.00 |
In 2020, the European Commission adopted the Taxonomy Regulation (EU) 2020/852. This regulation is one of the main actions of the European Union's Sustainable Finance Action Plan (SFAP), which is part of the European Green Deal. With this plan the European Union seeks to direct investment flows towards activities aligned with sustainable development and to contribute to the transition towards a greener and more sustainable economy
The Taxonomy is a classification system for determining whether an investment or economic activity is considered environmentally sustainable. In essence, it seeks to provide a common and transparent framework for companies and investors to assess and report on the environmental impact of their economic activities. Specifically, entities are asked to report on the proportion of the turnover of such large non-financial companies, their capital expenditure (hereafter "CapEx") or their operating expenses (hereafter "OpEx") associated with environmentally sustainable economic activities1 .
The Taxonomy covers various economic sectors and activities, setting out specific and detailed criteria for assessing their contribution to six environmental objectives:
The Taxonomy Regulation is set out in various delegated regulations2 and annexes that elaborate on the economic activities that can be considered sustainable in relation to the six environmental objectives mentioned above. And it details the technical criteria that activities must meet to determine their significant contribution to any of the six objectives, as well as the criteria for assessing that the activity do not cause significant harm (DNSH) to any of the other environmental objectives.
In this context, the group has carried out an analysis of its economic activities to determine whether any of them can be considered environmentally sustainable. It has been concluded that, in 2024, the main business activity, the manufacture of medicines, is an eligible, non-aligned activity. Additionally, several economic activities not directly relating to its main activity were qualified as eligible under the Taxonomy due to their connection with incurred expenses or investments during 2024.
| Revenue (Turnover) | CapEx | OpEx | |
|---|---|---|---|
| Eligibility in figures (EUR) | 4,740,499,195 | 297,944,613 | 144,052,948 |
| % Eligibility | 65.73% | 62.30% | 72.15% |
| Alignment in figures (EUR) | 0 | 78,436 | 0 |
| % Alignment | 0% | 0% | 0% |
1. The Taxonomy Regulation establishes criteria for using figures related turnover, CAPEX, OPEX and turnover that differ from traditional concepts. For this reason, there may be disparities between the figures used to calculate the Taxonomy compared to those presented elsewhere in Grifols' report.
| Target | Activity | Brief description according to the Regulation |
Brief description according to Grifols' activity |
|---|---|---|---|
| Sustainable use and protection of water and marine resources |
2.2 Urban waste water treatment |
The operation of urban wastewater infrastructure, including treatment plants, sewer networks, storm water management structures, connections to wastewater infrastructure, decentralized wastewater treatment facilities, as well as treated effluent discharge structures |
The Biopharma business unit's main production plants, located in Barcelona (Spain) and Clayton (North Carolina, USA), have on-site wastewater treatment plants to reduce COD before discharge to the public sewer. For more information see: "Water pollution". |
| Pollution prevention and control |
1.2. Manufacture of medicinal products |
Manufacture of medicinal products. | Grifols' core business, which consists of producing plasma-derived medicines and other solutions. |
| Protection and restoration of biodiversity and ecosystems |
1.1. Conservation, including the recovery of habitats, ecosystems and species |
Initiation, development and implementation, either independently or on commission or by contract, of conservation activities, including restoration activities to maintain or improve the conditions and trends of land, freshwater and marine habitats, ecosystems, and their related flora and fauna populations. |
Grifols owns more than 120 hectares of protected forest in Clayton, North Carolina (U.S.) located near its production complex. More information: "Biodiversity protection and conservation programs." |
To determine eligibility, the analysis focused on identifying economic activities contributing to key performance indicators (KPIs) – turnover, CapEx, and OpEx – that align with the activities specified in the Climate Delegated Act (2021/2139) and its amendments (2023/2485).
The main activity, manufacture of medicines, is described in the Taxonomy regulation. Specifically, it consists of activity 1.2. Manufacture of medicinal products, which falls under the environmental objective of Pollution prevention and control.
Additionally, other secondary economic activities of the company have been identified that are not directly related to its core business but are related to investments (CapEx) or expenditures (OpEx) made in 2024 and are therefore also considered eligible under the Taxonomy.
In accordance with the Taxonomy Regulation for the fiscal year 2024, the alignment of those activities that can contribute to one of the 6 objectives has been assessed. This assessment has been carried out taking into account the three conditions that an economic activity must meet to be considered environmentally sustainable:
As a result of the alignment analysis, it has been concluded that Grifols' main activity is not aligned with the Taxonomy, and that it contributes to the objective "Sustainable use and protection of water resources" with one of its eligible secondary activities.
● The main activity, 1.2 Manufacture of medicinal products, is not aligned with the Taxonomy, as it does not meet the criterion of Not causing significant harm to the climate change mitigation objective. This is due to the fact that the production of plasma derivatives requires a multi-stage cold chain that starts with obtaining the raw material, passing through manufacturing and finally storage and dispatch of the finished product. Raw material procurement, transport and storage in Plasma Logistics Centres (PLC) is common to all blood products and is carried out at -30ºC/-35ºC. Climate change mitigation criteria require that pharmaceutical products requiring refrigeration use a refrigerant gas with a GWP of 150 or lower, this level of GWP can only be achieved with ammonia and/or CO2 based solutions. This is the standard for Grifols' new facilities in a large part of the cold chain; however, to date, Grifols does not has any product which throughout its cold chain is manufactured 100%, at all stages, using refrigerant gases with a GWP of less than 150.
The calculation of the turnover ratio, as defined in Article 8(2)(a) of Regulation (EU) 2020/852, takes into account the proportion of turnover derived from products or services associated with economic activities deemed environmentally sustainable under the EU Taxonomy (numerator), divided by net turnover (denominator), as defined in Article 2(5) of Directive 2013/34/EU.
Turnover includes income recognized by International Accounting Standard (IAS) 1, paragraph 82(a), adopted by Commission Regulation (EC) No. 1126/2008. In Grifols' case, the numerator includes the sum of turnover (as reflected in the International Financial Reporting Standards adopted by the European Union (IFRS–EU) group 70) associated with accounts considered eligible from a taxonomy perspective.
With regard to the numerator of the turnover KPI, Grifols has identified as eligible activity 1.2 Manufacture of medicinal products under the objective of Pollution prevention and control, and has therefore taken into consideration the income related to the manufacturing activities of plasmaderived products and other medicines produced almost entirely by the Plasma Procurement and Biopharma division.
In addition, this year the group has further analyzed the companies engaged in the manufacture of medicines. As a result of this analysis, the figures corresponding to the economic activities of distribution and marketing of products, which in the 2023 taxonomy report were included in the "Manufacture of medicines" activity, have been excluded from the eligible activity 1.2. For this reason, the comparative figures reported in the 2023 taxonomy tables have been restated.
The figure in the denominator of the taxonomy tables coincides with the total turnover included in the consolidated profit and loss account of the consolidated annual accounts of the Grifols Group3 .
As stipulated in Article 8(2)(b) of Regulation (EU) 2020/852, the CAPEX ratio is calculated by dividing the numerator by the denominator, with the denominator representing the additions to tangible and intangible assets during the relevant period before depreciation, amortization and any possible revaluations, including those resulting from revaluations and impairments, corresponding to the relevant period, excluding changes in fair value. The denominator will also include additions to tangible and intangible assets resulting from business combinations.
Regarding the numerator, it consists only of the aggregation of the CapEx of the activities considered eligible from a taxonomic point of view. For the activity of 1.2 Manufacture of medicinal products, the same considerations have been applied as previously explained in the point "Calculation of the percentage of turnover".
And the denominator corresponds to the total CapEx of the Grifols group, which includes investments in intangible assets, investments in property, plant and equipment and investments in assets for right of use 4 .
In adherence to Article 8(2)(b) of Regulation (EU) 2020/852, the OPEX ratio is calculated by dividing the numerator by the denominator. The OPEX denominator includes direct non-capitalized costs related to research and development, building-renovation measures, short-term leases, maintenance and repairs, and other direct expenses linked to the daily maintenance of tangible fixed assets, whether performed by the company itself or by third-party subcontractors, to ensure their continued and effective operation.
In this case, for the calculation of the OpEx indicator, the following have been considered:
It should be noted that expenses related to the routine maintenance of tangible fixed assets, such as cleaning services or repairs to computer systems, were excluded from the numerator calculation, in accordance with Article 8 of the regulation and the accounting methodology adopted by Grifols for presenting these expenses.
In line with the principle of prudence, expense accounts lacking sufficient detail to determine whether they were related to maintenance directly linked to the analyzed taxonomic activities, or other types of maintenance, were not considered eligible.
Accordingly, the denominator of the indicator encompasses the expenditure composed of the three concepts described above, while the numerator is the expenditure only of the activities that have been recognized as eligible according to the established criteria. For the activity of 1.2 Manufacture of medicinal products, the same considerations have been applied as previously explained in the point "Calculation of the percentage of turnover".
The following tables show the data corresponding to the Turnover, CapEx and OpEx of Grifols' corresponding economic activities that comply with the European Taxonomy. Consistent with the rest of the Consolidated Statement of Non-Financial Information and Sustainability Information, Grifols presents the taxonomy tables for Grifols and Biotest separately.
| Economic Activities (1) Code Turnover (3) Proportion Proportion of Taxonomy-aligned (A,1) or (2) of Turnover -eligible (A.2.) turnover, 2023 (18) 2023 (4) Category transitional activity (20 Category enabling activity (19) Climate Change Mitigation (11) Climate Change Adaption (12) Climate Change Mitigation (5) Climate Change Adaption (6) Minimum Safeguards (17) Circular Economy (15) Circular Economy (9) Biodiversity (10) Biodiversity (16) Pollution (14) Pollution (8) Water (13) Water (7) S; N; N/EL (b) (c) S; N; N/EL (b) (c) S; N; N/EL (b) (c) S; N; N/EL (b) (c) S; N; N/EL (b) (c) S; N; N/EL (b) (c) Text EUR % S/N S/N S/N S/N S/N S/N S/N % F T A. TAXONOMY-ELIGIBLE ACTIVITIES A.1. Environmentally sustainable activities (Taxonomy-aligned) Turnover of environmentally sustainable 0 0 - - - - - - - - - - - - - 0% activities (Taxonomy-aligned) (A.1) Of which Enabling 0 0 - - - - - - - - - - - - - 0% F Of which Transitional 0 0 - - - - - - - - 0% T A.2 Taxonomy-Eligible but not environmentally sustainable activities (not Taxonomy-aligned activities) EL, EL, EL, EL, EL, EL, N/EL N/EL N/EL N/EL N/EL N/EL (f) (f) (f) (f) (f) (f) 1.2 Manufacture of medicinal products PPC 1.2 4,247,003,344.00 63.21% N/EL N/EL N/EL EL N/EL N/EL 68.80% Turnover of Taxonomy-eligible but not 4,247,003,344.00 63.21% 0% 0% 0% 63.21% 0% 0% 68.80% environmentally sustainable activities (not Taxonomy-aligned activities) (A.2) A. Turnover of Taxonomy 4,247,003,344.00 63.21% 0% 0% 0% 63.21% 0% 0% 68.80% eligible activities (A.1+A.2) B. TAXONOMY-NON-ELIGIBLE ACTIVITIES Turnover of Taxonomy non-eligible activities 2,471,794,187.00 36.79% TOTAL 6,718,797,531.00 100% |
Financial year 2024 | Year 2024 | Substantial Contribution Criteria | DNSH criteria ('Does Not Significantly Harm') | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Taxonomy
| Financial year 2024 | Year 2024 | Substantial Contribution Criteria | DNSH criteria ('Does Not Significantly Harm') | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Economic Activities (1) | Code (2) | CapEx (3) | Proportion o CapEx (4) |
Climate Change Mitigation (5) | Climate Change Adaption (6) | Water (7) | Pollution (8) | Circular Economy (9) | Biodiversity (10) | Climate Change Mitigation (11) | Climate Change Adaption (12) | Water (13) | Pollution (14) | Circular Economy (15) | Biodiversity (16) | Minimum Safeguards (17) | Taxonomy-aligned proportion of CapEx, 2023 (18) |
Category enabling activity (19) | Category transitional activity (20) |
| Text | EUR | % | S, N, N/EL (b) (c) | S, N, N/EL (b) (c) | S, N, N/EL (b) (c) | S, N, N/EL (b) (c) | S, N, N/EL (b) (c) | S, N, N/EL (b) (c) | S/N | S/N | S/N | S/N | S/N | S/N | S/N | % | F | T | |
| A. TAXONOMY-ELIGIBLE ACTIVITIES | |||||||||||||||||||
| A.1. Environmentally sustainable activities (Taxonomy-aligned) | |||||||||||||||||||
| 7.4 Installation, maintenance and repair of charging stations for electric vehicles in buildings (and parking spaces attached to buildings) |
CCM 7.4 | 78,436.00 | 0.02% | N/EL | N/EL | S | N/EL | N/EL | N/EL | S | S | S | S | S | S | S | 0% | ||
| CapEx of environmentally sustainable activi ties (Taxonomy-aligned) (A.1) |
78,436.00 | 0.02% | 0% | 0% | 0.02% | 0% | 0% | 0% | S | S | S | S | S | S | S | 0% | |||
| Of which Enabling | 0 | 0 | - | - | - | - | - | - | - | - | - | - | - | - | - | 0% | F | ||
| Of which Transitional | 0 | 0 | - | - | - | - | - | - | - | - | 0% | T | |||||||
| A.2 Taxonomy-Eligible but not environmentally sustainable activities (not Taxonomy-aligned activities) | |||||||||||||||||||
| EL. N/EL (f) |
EL. N/EL (f) |
EL. N/EL (f) |
EL. N/EL (f) |
EL. N/EL (f) |
EL; N/EL (f) |
||||||||||||||
| 1.2Manufacture of medicinal products |
PPC 1.2 | 262,523,450.72 | 61.94% | N/EL | N/EL | N/EL | EL | N/EL | N/EL | 50.80% | |||||||||
| CapEx of Taxonomy-eligible but not environmentally sustainable activities (not Taxonomy-aligned activities) (A.2) |
262,523,450.72 | 61.94% | 0% | 0% | 0% | 61.94% | 0% | 0% | 50.80% | ||||||||||
| A. CapEx of Taxonomy eligible activities (A.1+A.2) |
262,601,886.72 | 61.96% | 0% | 0% | 0.02% 61.94% | 0% | 0% | 50.80% | |||||||||||
| B. TAXONOMY-NON-ELIGIBLE ACTIVITIES | |||||||||||||||||||
| CapEx of Taxonomy non-eligible activities | 161,193,687.75 | 38.04% | Proportion of CapEx/Total CapEx | ||||||||||||||||
| TOTAL | 423,795,574.47 | 100% | Taxonomy-aligned per objective Taxonomy-eligible per objective |
| Proportion of CapEx/Total CapEx | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Taxonomy-aligned per objective | Taxonomy-eligible per objective | ||||||||||
| CCM | 0% | 0% | |||||||||
| CCA | 0% | 0% | |||||||||
| WTR | 0.02% | 0% | |||||||||
| PPC | 0% | 61.94% | |||||||||
| CE | 0% | 0% | |||||||||
| BIO | 0% | 0% |
Taxonomy
| Financial year 2024 | Year 2024 | Substantial Contribution Criteria | DNSH criteria ('Does Not Significantly Harm') | |||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Economic Activities (1) | Code (2) |
OpEx (3) | Proportion of OpEx 2023 (4) |
Climate Change Mitigation (5) | Climate Change Adaption (6) | Water (7) | Pollution (8) | Circular Economy (9) | Biodiversity (10) | Climate Change Mitigation (11) | Climate Change Adaption (12) | Water (13) | Pollution (14) | Circular Economy (15) | Biodiversity (16) | Minimum Safeguards (17) | Proportion of Taxonomy-aligned (A,1) or -eligible (A.2.) OpEx, 2023 (18) |
Category enabling activity (19) | Category transitional activity (20) | |
| Text | EUR | % | S, N, N/EL (b) (c) | S, N, N/EL (b) (c) | S, N, N/EL (b) (c) | S, N, N/EL (b) (c) | S, N, N/EL (b) (c) | S, N, N/EL (b) (c) S/N |
S/N | S/N | S/N | S/N | S/N | S/N | % | F | T | |||
| A. TAXONOMY-ELIGIBLE ACTIVITIES | ||||||||||||||||||||
| A.1. Environmentally sustainable activities (Taxonomy-aligned) | ||||||||||||||||||||
| OpEx of environmentally sustainable activities (Taxonomy-aligned) (A.1) |
0 | 0 | - | - | - | - | - | - | - | - | - | - | - | - | - | 0% | ||||
| Of which Enabling | 0 | 0 | - | - | - | - | - | - | - | - | - | - | - | - | - | 0% | F | |||
| Of which Transitional | 0 | 0 | - | - | - | - | - | - | - | - | 0% | T | ||||||||
| A.2 Taxonomy-Eligible but not environmentally sustainable activities (not Taxonomy-aligned activities) | ||||||||||||||||||||
| EL; N/EL (f) |
EL; N/EL (f) |
EL; N/EL (f) |
EL; N/EL (f) |
EL; N/EL (f) |
EL; N/EL (f) |
|||||||||||||||
| 1.2 Manufacture of medicinal products |
PPC 1.2 |
74,620,853.00 | 61.96% | N/EL | N/EL | N/EL | N/EL | N/EL | EL | 60.96% | ||||||||||
| 1.1 Conservation, including restoration, of habitats, ecosystems and species |
BIO 1.1 |
31,609.01 | 0.03% | N/EL | N/EL | N/EL | EL | N/EL | N/EL | 0.01% | ||||||||||
| OpEx of Taxonomy-eligible but not environmentally sustainable activities (not Taxonomy-aligned activities) (A.2) |
74,652,462.01 | 61.98% | 0% | 0% | 0% | 61.96% | 0% | 0.03% | 60.97% | |||||||||||
| A. OpEx of Taxonomy eligible activities (A.1+A.2)*1 |
74,652,462.01 | 61.98% | 0% | 0% | 0% | 61.96% | 0% | 0.03% | 60.97% | |||||||||||
| B. TAXONOMY-NON-ELIGIBLE ACTIVITIES | ||||||||||||||||||||
| OpEx of Taxonomy non-eligible activities | 45,785,320.29 | 38.02% | Proportion of OpEx/Total OpEx | |||||||||||||||||
| TOTAL 120,437,782.30 |
100% | Taxonomy-aligned per objective | Taxonomy-eligible per objective | |||||||||||||||||
| CCM | 0% | 0% |
CCA 0% 0% WTR 0% 0% PPC 0% 61.96% CE 0% 0.00% BIO 0% 0.03%
| Financial year 2024 | Substantial Contribution Criteria | DNSH criteria ('Does Not Significantly Harm') | |||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Economic Activities (1) | Code (2) |
Turnover (3) | Proportion of Turnover 2023 (4) |
Climate Change Mitigation (5) | Climate Change Adaption (6) | Water (7) | Pollution (8) | Circular Economy (9) | Biodiversity (10) | Climate Change Mitigation (11) | Climate Change Adaption (12) | Water (13) | Pollution (14) | Circular Economy (15) | Biodiversity (16) | Minimum Safeguards (17) | Proportion of Taxonomy-aligned (A,1) or -eligible (A.2.) turnover, 2023 (18) |
Category enabling activity (19) | Category transitional activity (20 |
| Text | EUR | % | S; N; N/EL (b) (c) | S; N; N/EL (b) (c) | S; N; N/EL (b) (c) | S; N; N/EL (b) (c) | S; N; N/EL (b) (c) | S; N; N/EL (b) (c) | S/N | S/N | S/N | S/N | S/N | S/N | S/N | % | F | T | |
| A. TAXONOMY-ELIGIBLE ACTIVITIES | |||||||||||||||||||
| A.1. Environmentally sustainable activities (Taxonomy-aligned) | |||||||||||||||||||
| Turnover of environmentally sustainable activities (Taxonomy-aligned) (A.1) |
0 | 0 | - | - | - | - | - | - | - | - | - | - | - | - | - | 0% | |||
| Of which Enabling | 0 | 0 | - | - | - | - | - | - | - | - | - | - | - | - | - | 0% | F | ||
| Of which Transitional | 0 | 0 | - | - | - | - | - | - | - | - | 0% | T | |||||||
| A.2 Taxonomy-Eligible but not environmentally sustainable activities (not Taxonomy-aligned activities) | |||||||||||||||||||
| EL, N/EL (f) |
EL, N/EL (f) |
EL, N/EL (f) |
EL, N/EL (f) |
EL, N/EL (f) |
EL, N/EL (f) |
||||||||||||||
| 1.2 Manufacture of medicinal products | PPC 1.2 | 493,495,851 | 100% | N/EL | N/EL | N/EL | EL | N/EL | N/EL | 71.28% | |||||||||
| Turnover of Taxonomy-eligible but not environmentally sustainable activities (not Taxonomy-aligned activities) (A.2) |
493,495,851 | 100% | 0% | 0% | 0% | 100% | 0% | 0% | 71.28% | ||||||||||
| A. Turnover of Taxonomy eligible activities (A.1+A.2) |
493,495,851 | 100% | 0% | 0% | 0% | 100% | 0% | 0% | 71.28% | ||||||||||
| B. TAXONOMY-NON-ELIGIBLE ACTIVITIES | |||||||||||||||||||
| Turnover of Taxonomy non-eligible activities | - | 0% | Proportion of turnover/Total turnover | ||||||||||||||||
| TOTAL | 493,495,851 | 100% | Taxonomy-aligned per objective | Taxonomy-eligible per objective | |||||||||||||||
| CCM CCA |
0% 0% |
0% 0% |
WTR 0% 0% PPC 0% 100% CE 0% 0% BIO 0% 0%
Taxonomy
| Financial year 2024 | Substantial Contribution Criteria | DNSH criteria ('Does Not Significantly Harm') | |||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Economic Activities (1) | Code (2) | Year 2024 CapEx (3) |
|||||||||||||||||
| Proportion o CapEx (4) |
Climate Change Mitigation (5) | Climate Change Adaption (6) | Water (7) | Pollution (8) | Circular Economy (9) | Biodiversity (10) | Climate Change Mitigation (11) | Climate Change Adaption (12) | Water (13) | Pollution (14) | Circular Economy (15) | Biodiversity (16) | Minimum Safeguards (17) | Taxonomy-aligned proportion of CapEx, 2023 (18) |
Category enabling activity (19) | Category transitional activity (20) | |||
| Text | |||||||||||||||||||
| EUR | % | S, N, N/EL (b) (c) | S, N, N/EL (b) (c) | S, N, N/EL (b) (c) | S, N, N/EL (b) (c) | S, N, N/EL (b) (c) | S, N, N/EL (b) (c) | S/N | S/N | S/N | S/N | S/N | S/N | S/N | % | F | T | ||
| A. TAXONOMY-ELIGIBLE ACTIVITIES | |||||||||||||||||||
| A.1. Environmentally sustainable activities (Taxonomy-aligned) | |||||||||||||||||||
| CapEx of environmentally sustainable activi ties (Taxonomy-aligned) (A.1) |
0 | 0 | 0% | 0% | 0.03% | 0% | 0% | 0% | S | S | S | S | S | S | S | 0% | |||
| Of which Enabling | 0 | 0 | - | - | - | - | - | - | - | - | - | - | - | - | - | 0% | F | ||
| Of which Transitional | 0 | 0 | - | - | - | - | - | - | - | - | 0% | T | |||||||
| A.2 Taxonomy-Eligible but not environmentally sustainable activities (not Taxonomy-aligned activities) | |||||||||||||||||||
| EL. N/ EL (f) |
EL. N/ EL (f) |
EL. N/ EL (f) |
EL. N/ EL (f) |
EL. N/ EL (f) |
EL; N/ EL (f) |
||||||||||||||
| 1.2 Manufacture of medicinal products |
PPC 1.2 | 34,042,463.00 | 62.58% | N/EL | N/EL | N/EL | EL | N/EL | N/EL | 59,81% | |||||||||
| 4.1 Electricity generation using solar photovoltaic technology |
CCM 4.1 | 7,793.00 | 0.01% | EL | N/EL | N/EL | N/EL | N/EL | N/EL | 1,35% | |||||||||
| 4.25 Production of heat/cool using waste heat |
CCM 4.25 | 279,282.15 | 0.51% | EL | N/EL | N/EL | N/EL | N/EL | N/EL | 0,53% | |||||||||
| 6.5 Transport by motorbikes, pas senger cars and light commercial vehicles |
CCM 6.5 | 379,336.35 | 0.70% | EL | N/EL | N/EL | N/EL | N/EL | N/EL | 0,71% | |||||||||
| 6.6 Freight transport services by road |
CCM 6.6 | 135,403.84 | 0.25% | EL | N/EL | N/EL | N/EL | N/EL | N/EL | * | |||||||||
| 7.2 Renovation of existing buildings | CCM 7.2 | 23,000.00 | 0.04% | EL | N/EL | N/EL | N/EL | N/EL | N/EL | * | |||||||||
| 7.5 Installation, maintenance and repair of instruments and devices for measuring, regulation and controlling energy performance of buildings |
CCM 7.5 | 156,882.74 | 0.29% | EL | N/EL | N/EL | N/EL | N/EL | N/EL | 0,13% | |||||||||
| 8.1 Data processing, hosting and related activities |
CCM 8.1 | 318,565.00 | 0.59% | EL | N/EL | N/EL | N/EL | N/EL | N/EL | 0,38% | |||||||||
| CapEx of Taxonomy-eligible but not environmentally sustainable activities (not Taxonomy-aligned activities) (A.2) |
35,342,726.08 | 64.97% | 2% | 0% | 0% | 63% | 0% | 0% | 64,03% | ||||||||||
| A. CapEx of Taxonomy eligible activities (A.1+A.2) |
35,342,726.08 | 64.97% | 2% | 0% | 0% | 63% | 0% | 0% | 64,03% | ||||||||||
| B. TAXONOMY-NON-ELIGIBLE ACTIVITIES | |||||||||||||||||||
| CapEx of Taxonomy non-eligible activities | 19,051,820.07 | 35.03% | Proportion of CapEx/Total CapEx | ||||||||||||||||
| TOTAL | 54,394,546.15 | 100% | Taxonomy-aligned per objective | Taxonomy-eligible per objective |
| Proportion of CapEx/Total CapEx | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Taxonomy-aligned per objective | Taxonomy-eligible per objective | ||||||||||
| CCM | 0% | 2% | |||||||||
| CCA | 0% | 0% | |||||||||
| WTR | 0% | 0% | |||||||||
| PPC | 0% | 63% | |||||||||
| CE | 0% | 0% | |||||||||
| BIO | 0% | 0% |
| Financial year 2024 | Substantial Contribution Criteria | DNSH criteria ('Does Not Significantly Harm') | |||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Economic Activities (1) | Code (2) | Year 2024 OpEx (3) |
Proportion | ||||||||||||||||
| of OpEx 2023 (4) |
Proportion of Taxonomy-aligned (A,1) or | ||||||||||||||||||
| Climate Change Mitigation (5) | Climate Change Mitigation (11) | Climate Change Adaption (12) | -eligible (A.2.) OpEx, 2023 (18) | Category enabling activity (19) | Category transitional activity (20) | ||||||||||||||
| Climate Change Adaption (6) | Minimum Safeguards (17) | ||||||||||||||||||
| Water (7) | Pollution (8) | Circular Economy (9) | Biodiversity (10) | Water (13) | Pollution (14) | Circular Economy (15) | Biodiversity (16) | ||||||||||||
| S, N, N/EL (b) (c) | S, N, N/EL (b) (c) | S, N, N/EL (b) (c) | S, N, N/EL (b) (c) | S, N, N/EL (b) (c) | S, N, N/EL (b) (c) | ||||||||||||||
| Text | EUR | % | S/N | S/N | S/N | S/N | S/N | S/N | S/N | % | F | T | |||||||
| A. TAXONOMY-ELIGIBLE ACTIVITIES | |||||||||||||||||||
| A.1. Environmentally sustainable activities (Taxonomy-aligned) | |||||||||||||||||||
| OpEx of environmentally sustainable activities (Taxonomy-aligned) (A.1) |
0 | 0 | - | - | - | - | - | - | - | - | - | - | - | - | - | 0% | |||
| Of which Enabling | 0 | 0 | - | - | - | - | - | - | - | - | - | - | - | - | - | 0% | F | ||
| Of which Transitional | 0 | 0 | - | - | - | - | - | - | - | - | 0% | T | |||||||
| A.2 Taxonomy-Eligible but not environmentally sustainable activities (not Taxonomy-aligned activities) | |||||||||||||||||||
| EL; N/EL (f) |
EL; N/EL (f) |
EL; N/EL (f) |
EL; N/EL (f) |
EL; N/EL (f) |
EL; N/EL (f) |
||||||||||||||
| 1.2 Manufacture of medicinal products |
PPC 1.2 | 64,792,030.28 | 81.81% | N/EL | N/EL | N/EL | EL | N/EL | N/EL | 89.22% | |||||||||
| 2.4 Remediation of contaminated sites |
PPC 2.4 | 41,313.54 | 0.05% | N/EL | N/EL | N/EL | EL | N/EL | N/EL | 0.04% | |||||||||
| 4.9 Transmission and distribution of electricity |
CCM 4.9 | 102,794.93 | 0.13% | EL | N/EL | N/EL | N/EL | N/EL | N/EL | 0.13% | |||||||||
| 4.30 High-efficiency co-generation of heat/cool and power from fossil gaseous fuels |
CCM 4.30 | 162,876.30 | 0.21% | EL | N/EL | N/EL | N/EL | N/EL | N/EL | 0.19% | |||||||||
| 5.3 Construction, extension and operation of waste water collection and treatment |
CCM 5.3 | 213,061.56 | 0.27% | EL | N/EL | N/EL | N/EL | N/EL | N/EL | 0.11% | |||||||||
| 6.5 Transport by motorbikes, passenger cars and light commercial vehicles |
CCM 6.5 | 184,205.91 | 0.23% | EL | N/EL | N/EL | N/EL | N/EL | N/EL | 0.30% | |||||||||
| 6.6 Freight transport services by road | CCM 6.6 | 47,508.92 | 0.06% | EL | N/EL | N/EL | N/EL | N/EL | N/EL | 0.10% | |||||||||
| 7.2 Renovation of existing buildings | CCM 7.2 | 23,000.00 | 0.03% | EL | N/EL | N/EL | N/EL | N/EL | N/EL | * | |||||||||
| 7.3 Installation, maintenance and repair of energy efficiency equipment |
CCM 7.3 | 2,655,850.94 | 3.35% | EL | N/EL | N/EL | N/EL | N/EL | N/EL | 2.82% | |||||||||
| 7.5 Installation, maintenance and repair of instruments and devices for measuring, regulation and controlling energy performance of buildings |
CCM 7.5 | 233,559.74 | 0.29% | EL | N/EL | N/EL | N/EL | N/EL | N/EL | 0.29% | |||||||||
| 8.1 Data processing, hosting and related activities |
CCM 8.1 | 944,283.86 | 1.19% | EL | N/EL | N/EL | N/EL | N/EL | N/EL | 0.53% | |||||||||
| OpEx of Taxonomy-eligible but not environmen tally sustainable activities (not Taxono my-aligned activities) (A.2) |
69,400,485.98 | 87.62% | 0% | 0% | 0% | 81.81% | 0% | 0.05% | 93.84% | ||||||||||
| A. OpEx of Taxonomy eligible activities (A.1+A.2)*1 |
69,400,485.98 | 87.62% | 0% | 0% | 0% | 81.81% | 0% | 0.05% | 93.84% | ||||||||||
| B. TAXONOMY-NON-ELIGIBLE ACTIVITIES | |||||||||||||||||||
| OpEx of Taxonomy non-eligible activities | 9,802,119.49 | 12.38% | Taxonomy-aligned per objective | Proportion of OpEx/Total OpEx Taxonomy-eligible per objective |
|||||||||||||||
| TOTAL | 79,202,605.47 | 100% | CCM | 0% | 6% | ||||||||||||||
| CCA | 0% | 0% |
WTR 0% 0% PPC 0% 81.86% CE 0% 0.00% BIO 0% 0.00%
Climate change is one of the world's most urgent challenges. Global temperatures have risen in recent decades, and most prediction models indicate a significant increase in greenhouse gas (GHG) concentrations, leading to continued global warming in the coming years.
Aware of the consequences of rising temperatures, Grifols has set clear targets to effectively reduce emissions; measures and manages its climaterelated impacts, risks and opportunities; and implements a climate policy and strategy. Grifols' climate strategy is driven by its Board of Directors.
Environmental governance at Grifols includes climate action. The company is committed to integrating sustainability into all operations and minimizing its environmental impact in alignment with global climate mitigation goals.
As part of this commitment, Grifols incorporates climate risk management into its governance and strategic planning model, considering both physical risks (e.g., extreme weather events) and transition risks such as regulatory and market shifts linked to climate policies. This approach enables the company to identify, assess and prioritize climate-related risks that could impact its operations, products and services.
More details: "Environmental Governance" section.
| E1 CLIMATE CHANGE |
||
|---|---|---|
| Material IROs | Typology | Description |
| CLIMATE CHANGE ADAPTATION | ||
| Increase in extreme weather events |
R Physical |
Climate change is altering weather patterns worldwide, with the most relevant impacts for Grifols being extreme precipitation and drought. Understanding current and potential physical climate risks is essential for managing the company's climate resilience. |
| CLIMATE CHANGE MITIGATION | ||
| Contribution to climate change from scope 1 and 2 GHG emissions |
- OO SP |
As a global company, Grifols recognizes that its activities generate greenhouse gas (GHG) emissions. The company is committed to advancing its climate action efforts by reducing its scope 1 and 2 emissions through proactive management. |
| Contribution to climate change from scope 3 GHG emissions |
- OO SP |
Scope 3 emissions account for approximately 80% of Grifols' total emissions, with Category 1 (purchased goods and services) being the largest contributor, followed by Category 4 (transportation). In the coming years, Grifols aims to implement targeted actions to reduce these indirect emissions. |
| Non-compliance with climate targets or legal requirements |
R Transition | Climate change and energy efficiency regulations are becoming increasingly stringent. Companies may face significant consequences if they fail to meet climate targets or environmental laws. For this reason, Grifols dedicates substantial efforts to ensuring compliance with its climate targets. |
| ENERGY | ||
| Non-renewable energy consumption | - + OO |
Grifols continues to expand its use of renewable energy, which now accounts for 44.6% of its electricity consumption. The company prioritizes Power Purchase Agreements (PPAs) to increase the share of renewable energy in the market. |
| Non-compliance with legal requirements |
R | Climate change and energy efficiency regulations are becoming increasingly strict. Companies may face significant consequences if they fail to comply with these regulations. |
| Insufficient energy supply | R | This refers to the risk of rising energy costs, production disruptions, and supply chain interruptions due to shortages of both renewable and non-renewable energy sources or price volatility. |
| + Positive impact - Negative impact R Risk OO Own Operation SP Supply Chain |
Since 2019, Grifols has regularly updated its climate risk map as part of its integrated approach to managing climate-related risks and opportunities. This framework helps the company determine whether a potential impact constitutes a material risk or opportunity.
In 2024, within the framework of the company's resilience assessment, Grifols conducted a Climate Risk and Opportunity Analysis based on recommendations from the international scientific community and the general criteria established by key reporting frameworks such as the CSRD. The analysis included a stressed pessimistic scenario4 (SSP5-8.5) from the IPCC to assess physical climate risks; a stressed optimistic scenario (NZS) from the IEA to evaluate transition risks; and a strategic analysis aligned with TCFD recommendations, based on a 2°C global warming scenario (SSP2-RCP-4.5).
The potential financial impacts of each material risk and opportunity have also been estimated.
For this process, 27 potential climate-related risks and opportunities were evaluated across the company's entire value chain, including suppliers (upstream), Grifols' own operations and infrastructure, and the distribution and use of its products (downstream). Following this analysis, 12 material risks and opportunities were identified: 2 physical risks, 6 transition risks and 4 opportunities.
| Analyzed dimension | ROCC typology | Selected scenarios | Short term |
Medium term |
Long term |
|---|---|---|---|---|---|
| Assets, business model (all economic activities) | Physical risks | SSP5-8.5 (IPCC) SSP24.5 (IPCC) |
2021-2040 | 2041-2060 | 2061-2100 |
| and supply chain | Transition risks and opportunities |
NZE*(IEA) | 2030 | 2050 | 2100 |
| Taxonomic activities | Physical risks | SSP5-4.5 (PCC) SSP24.5 (PCC) |
2021-2040 | 2041-2060** |
* The Net Zero Emissions by 2050 Scenario: A regulatory scenario that outlines a pathway for the global energy sector to achieve net-zero CO2 emissions by 2050, with advanced economies reaching net zero ahead of others.
** For taxonomy-aligned economic activities exceeding 10 years, the assessment is conducted using the latest generation of climate projections, including, at a minimum, climate projection scenarios covering 10 to 30 years.

| Typology | Risks | Description | Financial impact | Risk management and mitigation |
|
|---|---|---|---|---|---|
| Physical (acute) | Increase in frequency and intensity of heavy rainfall and flooding |
The frequency and intensity of extreme precipitation and flooding are expected to rise in many regions due to global warming. Grifols has facilities in some of these regions. |
Potential impacts include temporary production stoppages or a reduction in plasma collection due to donation center closures. This could lead to higher operational costs from relocating production to unaffected sites and lower revenue due to reduced plasma collection. |
Measures taken by Grifols to mitigate this risk are detailed in Section Climate Change Adaptation of this report. |
|
| Physical (chronic) |
Reduced water availability in operations and supply chain |
These risks could result in an increase in costs associated with water resource procurement, a |
|||
| Transition (policy & legal) |
Need to implement changes in water management within operations |
Grifols operates in areas where, under the simulated scenario, water access could become more challenging or water management regulations could change. |
reduction in revenue due to a decline in production capacity, and necessary investments to optimize the water cycle in processes and facilities. This includes improving consumption efficiency, enhancing the treatment process, and, where possible, reusing water resources. |
Measures taken by Grifols to mitigate this type of risk are detailed in Section Water Resources of this report. |
|
| Transition (technological) |
Shift toward low-emission technologies |
The company may need to implement low- or zero-emission technologies across its processes and facilities to comply with regulations and climate targets. |
Greater investments are required | Various emissions reduction and energy efficiency measures are outlined throughout the Environmental section of this report and in the Environmental Program. Exposure to this risk is expected to decrease as Grifols meets its targets. |
|
| Transition (market/ reputation) |
Failure to meet greenhouse gas (GHG) reduction targets |
Risk of non-compliance with scope 1 and 2 decarbonization targets set by Grifols |
to reduce both direct and indirect emissions in compliance with regulations and climate targets. |
||
| Transition (market/ reputation) |
Suppliers failing to meet company defined climate targets |
Potential non-compliance by suppliers with Grifols' GHG reduction targets, which could impact the company's ability to achieve its own scope 3 emissions reductions. |
These include HVAC system upgrades, boiler modernization, renewable energy generation, aimed at lowering Grifols' emissions and increasing energy efficiency. Additionally, further investment would be needed |
||
| Transition (policy & legal) |
Changes in regulatory and reputational requirements for emissions reduction. |
Climate change and energy efficiency regulations are becoming increasingly stringent in some of the regions where Grifols operates. |
to offset the carbon footprint in case of non-compliance with decarbonization targets. |
||
| Transition (policy & legal) |
Increase in corporate carbon footprint costs |
Rising costs due to the increasing price of carbon offset credits. |
Grifols has also identified four material opportunities related to climate change. The first two are linked to resource efficiency, while the latter two focus on the transition to renewable energy:
| Material Sub-topic | Policies | Actions | Metrics and Targets |
|---|---|---|---|
| Climate Change Adaptation & Mitigation |
• Climate Action Policy • Environmental Policy • 2023-2026 Corporate Environmental Program |
• Formalize environmental programs aligned with Grifols' commitments (Grifols 2030 Agenda and SBTi) • Periodically review climate-related risks and opportunities • Monitor climate commitments in meetings of the Board of Directors' Sustainability Committee, the Sustainability Steering Committee, and the Environmental Committees of each company |
Based on SBTi: • Reduce absolute scope 1 and 2 GHG emissions by 42% by 2030, using 2022 as the baseline year • Reduce absolute scope 3 GHG emissions by 25% within the same timeframe Based on the Grifols 2030 Agenda: • Reduce GHG emissions per unit of production by 55% by 2030, compared to 2018 levels Based on the 2023-2026 Corporate Environmental Program: • Cut CO2 e emissions by 60,000 t/year through increased renewable energy production and eco-efficiency measures (scope 1 and 2) • Decarbonization initiatives for business travel, employee transportation, and waste management Achieve net-zero emissions by 2050 (scopes 1 and 2) |
| Energy | • Energy Policy | • Promote efficient energy use. • Obtain LEED certification for buildings and offices • Sign Power Purchase Agreements (PPAs) for renewable energy • Operate cogeneration plants |
• Increase energy efficiency per unit of production by 15% (+5% by 2030) • Source 100% of electricity from renewable energy by 2030 |
Grifols' Climate Action Policy provides a framework for developing a cohesive strategy and business model aligned with its commitment to addressing climate change. It is fully integrated with the Sustainability Policy, Environmental Policy and Energy Policy.
Grifols' climate-related policies explicitly cover climate change mitigation and adaptation, energy efficiency and the promotion of renewable energy. They also establish a framework for enhancing communication, awareness and climate education among Grifols' workers.
The company allocates significant resources to environmental management, with approximately 39% dedicated to climate action.

For a detailed report on resources allocated to environmental activities, see the tables at the end of this section.
The primary climate adaptation risks correspond to the physical risks identified in the Climate Risk and Opportunity Analysis presented earlier. Specifically, two material risks were identified: an increase in the frequency and intensity of heavy rainfall and flooding, and reduced water availability in operations and the supply chain.
The first and most critical step is the analysis and identification of climate-related physical risks that could impact Grifols. As outlined at the beginning of this section, the company conducts an annual Climate Risk and Opportunity Analysis. In collaboration with insurers, Grifols also conducts periodic assessments of its key assets to identify adaptation measures that enhance the resilience of its most critical infrastructure. In turn, this approach reinforces the climate resilience of Grifols' business model.
In line with its internal risk management procedures, Grifols diversifies its production sites, establishes contingency and emergency plans, selects durable materials and designs new facilities to ensure its infrastructure is well prepared for extreme weather events, including strong winds and flooding.
For example, Grifols' production plant in Barcelona is located near a river. While there is no historical record of flooding at the site and its probability remains low, Grifols has taken preventive measures to mitigate any potential impact. Similarly, in the United States, the company has reinforced roof structures in facilities vulnerable to high winds.
Additionally, when selecting locations for new facilities, Grifols prioritizes geographic areas that are less exposed to natural hazards, reducing the risk of flooding and other physical climate-related threats. The company's Environmental Program also includes additional adaptation measures to further enhance its resilience to climate-related risks.
More information on the achievement of targets set in environmental programs: "Climate Change Mitigation" section.
The key risks associated with climate change mitigation align with the transition risks identified in the Climate Risk and Opportunity Analysis. Specifically, six material risks were recognized: failure to meet greenhouse gas (GHG) reduction targets; the need to implement changes in water management within operations; changes in regulatory and reputational requirements for emissions reduction; the transition to low-emission technologies; suppliers failing to meet the company's climate targets; the need to implement changes in waste management within operations; and increased costs associated with the corporate carbon footprint.
Mitigation efforts focused on the following points to ensure alignment of Grifols' strategy and business model with the transition to a sustainable economy, as well as the Paris Agreement's goal of limiting global warming to 1.5°C and achieving climate neutrality by 2050:
The company has also begun working on a Transition Plan to achieve climate neutrality by 2050, which it expects to adopt within the next two years.
Climate change is one of the three key cornerstones addressed in Grifols' 2023-2026 Corporate Environmental Program, which also sets specific targets and decarbonization initiatives aimed at reducing GHG emissions and mitigating climate change, supporting the transition to a low-carbon economy. The company evaluates and monitors progress toward the objectives outlined in its environmental programs, which in turn help mitigate key physical risks and leverage major transition opportunities.

| DEGREE OF COMPLIANCE WITH ACTIONS AS OF YEAR-END 2024 57.81% |
||
|---|---|---|
| Climate change mitigation objectives | ||
| RENEWABLE ENERGY | ||
| Sign Power Purchase Agreements (PPAs) for the purchase of 169,000 MWh of renewable electricity annually in Spain and the U.S. Reduction of 56,960 metric tons of CO2 e per year. |
||
| Implement on-site renewable energy generation projects with a total capacity of 500 kW. Reduction of 132 metric tons of CO2 e per year. |
||
| ENERGY EFFICIENCY IMPROVEMENTS | ||
| Apply artificial intelligence measures in chilled water control systems. Electricity saving of 4,170 MWh/year. Reduction of 1,333 t metric tons of CO2 e per year. |
||
| Implement measures to reduce heat energy consumption for hot water production. Electricity saving of 3.300 MWh/year. Reduction of 598+ metric tons of CO2 e per year. |
||
| Improve energy efficiency in industrial cooling systems by centralizing glycol generation circuits at -20°C and 0°C. Electricity saving of 3.500 MWh/year. Reduction of 525+ metric tons of CO2 e per year. |
||
| Reduce CO2e emissions by 60,000 metric tons per year through increased renewable energy production and the implementation of eco-efficiency measures (scopes 1 and 2). |
Enhance energy efficiency in cooling towers. Electricity saving of 990 MWh/year. Reduction of 149 metric tons of CO2 e per year. |
|
| Optimize energy use in Diagnostic facilities in Barcelona (Spain), including buildings, water treatment circuits for injection, and air treatment systems for production areas. Electricity saving of 600+ MWh/year. Reduction of 95 metric tons of CO2 e per year. |
||
| Recover biomethane generated in the new wastewater treatment plant for use as boiler fuel. Electricity saving of 450 MWh/year. Reduction of 80 metric tons of CO2 e per year. |
||
| Optimize energy use in -30°C plasma storage warehouses. Electricity saving of 120+ MWh/year. Reduction of 33 metric tons of CO2 e per year. |
||
| Upgrade plastic bag forming machines for intravenous solutions to reduce electricity consumption. Electricity saving of 180 MWh/year Reduction of 26 metric tons of CO2 e per year. |
||
| Implement energy-saving measures, including LED lighting installation, sunshades on windows, and refrigeration system upgrades. Electricity saving of 74 MWh/year. Reduction of 25 metric tons of CO2 e per year. |
||
| Install LED lighting as part of energy-saving initiatives. Reduction of 18 metric tons of CO2 e per year. |
||
| Progressively replace electric motors with more efficient models. Electricity saving of 0.1 MWh/year. Reduction of 0.02 metric tons of CO2 e per year. |
||
| Conduct energy efficiency audits. | ||
| Reduce CO2 e emissions from refrigerant gas leaks by replacing them with gases with a lower Global Warming Potential (GWP). |
||
| Obtain LEED certification for new buildings. Reduction of 149 metric tons of CO2 e per year. |
||
| Maintain or increase remote work where feasible across Grifols' facilities. | ||
| Maintain or increase use of video calls to reduce air travel. | ||
| Decarbonization of business travel, |
Reduce CO2 e emissions per km from the company's rental car fleet by applying environmental criteria in contracts. |
|
| workers' transport and waste management |
Reduce supply chain transport emissions through agreements with logistics operators. | |
| Optimize waste storage to reduce collection frequency. Reduction of 1.2 metric tons of CO2 e per year. |
Grifols is aligned with the United Nations 2030 Agenda for Sustainable Development. In 2021, the company established 30 corporate objectives aligned with the UN Sustainable Development Goals (SDGs) as part of its sustainability strategy. Among these specific and measurable objectives are those related to climate change and decarbonization. The company's action plan to reduce GHG emissions per unit of production by 55% by 2030 compared to 2018 includes the following initiatives:
| PROGRESS IN 2024 | |
|---|---|
| Reduction in air travel | Air travel has continued to decline in 2024, down 31% from 2023 and 57% from pre-pandemic |
| levels (2019). The number of video calls made in 2024 increased by 95% compared to 2019 and 41% higher than in 2023. This has helped to minimize travel among Grifols' different locations. |
|
| Increase in remote work | Since 2022, Grifols has implemented a flexible work policy regulating remote work arrangements. In 2024, the number of people connected remotely has increased by 39% compared to 2023, exceeding 4,000 people on average per day. |
| Optimizing logistics | Since 2021, Grifols has been working to optimize its plasma transport network in Europe with the aim of reducing environmental impact. Recent initiatives include maximizing available space in transport containers, increasing the amount of plasma transported per container by 6.8%, therefore reducing total transport figures. Other ongoing measures include optimizing the frequency of plasma collection routes in European workplaces, promoting full truckloads between plasma collection points, warehouses and the Barcelona manufacturing complex and using larger U.S. pallets to optimize storage and transport, among others. |
| Minimizing the impact of workers' travel |
Grifols works to reduce the impact of emissions resulting from workers' commutes. The Barcelona facilities offer various bus services to coincide with different shift times, while in North Carolina, Grifols co-funds a shared transport service. |
| In recent years, electric vehicle chargers have been installed in the main workplaces. The company is working on a global vehicle fleet policy to promote the use of low-emission vehicles. |
|
| Commitment to renewable energies |
Grifols is reducing its emissions and increasingly relying on renewable energies, which now account for 44.6% of energy consumption. The goal is to reach 100% by 2030, which will require purchasing green energy and promoting new electricity-generation assets. |
| The company also reinforced its commitment to renewable energies by signing Power Purchase Agreements (PPAs) in the countries where it has a major industrial presence. Grifols' Casa Valdés photovoltaic plant in Spain became operational in 2022 and was included in the 10-year PPA signed with RWE in 2021. The agreement included a purchase of 26 million kWh per year, which will avoid 5,200 t of carbon emissions. |
|
| In 2024, more than 50.3 million kWh of renewable energy was consumed in Spain. In the U.S., over 132 million kWh of electricity was consumed with guaranteed renewable energy, and in Ireland, more than 9.5 million kWh. |
For further details, see tables at the end of this chapter.
In 2024, Grifols' science-based short-term emission reduction targets were approved by the Science Based Targets initiative (SBTi). SBTi evaluated Grifols' scope 1, 2, and 3 targets, confirming their alignment with global climate action and support of the Paris Agreement's goal of limiting global warming to 1.5°C this century.
In compliance with SBTi criteria, Grifols publishes detailed annual progress reports with a clear description of its targets, specifying details such as target type, coverage, baseline year and target year. The report also outlines progress made since the baseline year, reflecting emission reductions, increased use of renewable electricity and commitments with business partners, as well as implemented or planned actions to achieve these targets.
Grifols' GHG emissions inventory covers all scopes (1, 2, and 3) and categories, following the GHG Protocol and encompassing all company activities.
The company will review its targets every five years or whenever significant changes occur in its structure, inventory or baseline data, which may require recalculating and revalidating the targets.
Grifols commits to reduce absolute scope 1 and 2 GHG emissions 42% by 2030 from a 2022 base year. The target boundary includes biogenic land-related emissions and removals from bioenergy feedstocks.
Grifols commits to reduce absolute scope 3 GHG emissions from purchased goods and services, capital goods, fuel- and energy-related activities, and upstream transportation and distribution 25% by 2030 from a 2022 base year.
The Biotechnology Innovation Organization (BIO) advocates for biotechnological solutions in four key areas: sustainable biomass production, promoting sustainable production, developing lower carbon products and improving carbon capture. Grifols also belongs to other global organizations such as MedTech Europe or Asebio, who prioritize climate change mitigation in their operations.
More information on associations: "About this Report" section.
As a global company, Grifols recognizes that its activities generate GHG emissions and remains committed to advancing its climate action efforts by reducing its scope 1 and 2 emissions. To achieve this, the company not only measures and analyzes its emissions but also promotes active management strategies to mitigate them.
180,165 t CO2e scopes 1 and 2 (market based) 1,231,771 t CO2e total emissions 183.33 GHG intensity based on net revenue 3% Reduction in CO2e emission intensity for scopes 1, 2 and 3

Scope 1 Scope 2 (Market-based) Scope 3
Grifols uses the GHG Protocol Corporate Accounting and Reporting Standard methodology to calculate its carbon footprint and identify the greenhouse gas emissions (GHG) generated by its business activity.
The data reported includes all Grifols' global facilities, as well as acquisitions in 2023 and commercial subsidiaries with more than 10 employees.
Grifols has published its scopes 1 and 2 CO2 e emissions since 2011 and a thorough scope 3 inventory since 2021, with a focus on the highest priority categories. In this regard, it has quantified and conducted regular screening and materiality assessments in line with GHG Protocol.
Grifols has defined decarbonization targets for scopes 1, 2 and 3. Updated every three years, the Corporate Environmental Program outlines short-term intermediate decarbonization targets and milestones.
The company has clear goals established in its 2030 Agenda. Additionally, in 2024, its short-term emission reduction targets, aligned with the 1.5°C pathway, were approved by SBTi.
At present, the company does not hold carbon credits. Nonetheless, it applies an internal carbon price when making key decisions, such as designing new facilities and processes or replacing energy-consuming equipment. Carbon pricing has been factored into Grifols' investment strategy, helping assess the viability of new projects and promoting the profitability of energy efficiency and renewable energy initiatives.
Grifols is not included in the EU Carbon Market and not required to purchase emission allowances. However, as part of its transition plan, the company plans to establish a broader protocol in the coming years for incorporating carbon pricing into business decisions.
Regarding Grifols' locked-in emissions, these are primarily linked to natural gas infrastructure and facilities. However, they are not significant, around 5% of total emissions, and do not pose a risk to its short-term decarbonization targets.
* Scopes 1 and 2
For more details on the carbon footprint calculation, see the tables at the end of this section.
-2.9% vs 2023
56% natural gas
43% Electricity
1% other fuels
0% carbon
0% nuclear
*The remaining 22% of energy consumption corresponds to electricity and district heating, which is generated from renewable and non-renewable sources depending on the mix of each supplier
Consumption relative to sales
– Total energy consumption remained at similar levels to 2023, with a 2.5% decrease despite increased production.
This positive impact resulted in a 12% decrease in energy consumption relative to production in the Biopharma and Plasma Procurement business unit. Fossil sources: 56%
To avoid double accounting, total energy consumption includes the total natural gas consumed by Grifols, including cogeneration consumption, and subtracts the cogenerated electricity that is fed into the grid. All purchased electricity is included.
in each country.
-2% vs 2023

Biopharma+ Plasma procurement Diagnostic Commercial affiliates Bio Supplies Others Detailed natural gas consumption figures are included in the
● Diagnostic consumption levels increased by 2% and 7% relative to production and sales.
*In terms of consumption relative to production and sales, Biopharma includes the Plasma Procurement and Biopharma business units, which together would be comparable to the former Bioscience Division.
tables at the end of this chapter
380,344,448
Although to a lesser extent, Biopharma also consumes other fuels besides natural gas, including diesel, gasoline and propane to run its own generators, equipment and vehicles. In 2024, Biopharma consumed 4.3 million kWh of these fuels, in line with last year's figures (4.3 million kWh). Additionally, some of Grifols' German facilities use district heating for hot water and heating. In 2024, this system consumed 10.3 million kWh. Grifols' facilities do not consume coal or nuclear energy directly.

By 2030, 100% of the electricity consumed will come from renewable sources.
429 M kWh consumed
-4% vs 2023

| 28,799,845 | 27,076,568 | 27,102,724 |
|---|---|---|
| 17,863,379 | 17,130,922 | 16,915,870 |
| 3,776,145 | 3,121,378 | 3,172,283 |
| 545,997 | 2,560,933 | 2,047,710 |
| 2022 | 2023 | 2024 |
Biopharma+ Plasma procurement Diagnostic Commercial affiliates Bio Supplies Others
Detailed electricity consumption figures are included in the tables at the end of this chapter.
*In terms of consumption relative to production and sales, Biopharma includes the Plasma Procurement and Biopharma business units, which together would be comparable to the former Bioscience Division.
Artificial intelligence (AI) is enhancing the operational efficiency of Grifols plants. AI applications in the climate-control systems of its Parets del Vallès production plant (Barcelona, Spain) contributed to a 15% drop in energy consumption. In 2024, the project was implemented at the Biopharma facilities in Parets del Vallès, with further deployment planned for Biopharma facilities in North Carolina and Diagnostic facilities in San Diego in 2025.
Climate control is one of Grifols' main sources of electricity consumption, and technology can offer ways of reducing it, which inspired the launch of the "Energy Efficiency Through AI" pilot project in 2022.
44.6% of Grifols' total electricity consumption derives from renewable energy sources
Spain: 26.6% / U.S.: 68.8% / Ireland: 4.9%

Solar panels owned
In 2024, Grifols consumed a total of 191.7 million kWh of renewable electricity, representing 44.6% of total electricity consumption.
In Spain, 18.9 million kWh came from the Casa Valdés photovoltaic park, included in the 10-year clean energy supply contract (PPA) signed with RWE in 2021.
In 2024, a total of 417,413 kWh of photovoltaic energy was generated for self-consumption at Grifols' facilities in Barcelona and Murcia.
Grifols continues working toward agreements for the construction of new photovoltaic parks to increase renewable energy consumption in both Spain and the United States.
By region, the United States accounts for 70% of the group's electricity consumption, as it hosts several industrial complexes and most of Grifols' plasma donation centers. In 2024, 132 million kWh of electricity with a renewable energy guarantee was consumed (compared to 119 million kWh in 2023), while in Ireland, renewable electricity consumption exceeded 9.5 million kWh.
10% of total electricity consumption is generated at the Barcelona facility's cogeneration plant
Detailed figures on the cogeneration plant's consumption are included in the tables at the end of this chapter.
Biopharma's Barcelona facilities are equipped with a 6.1 MW cogeneration plant, which generates electricity sold back to the grid, as well as produces useful heat for Grifols' own facilities. This plant generated 43.4 million kWh of electricity in 2024, up 6.7% on the previous year.
The cogeneration plant was fully operational the entire year. The useful heat recovered amounted to 33.6 million kWh.
| GHG EMISSIONS (Gases de Efecto Invernadero) | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| % | 2024 | Spain | U.S. | RoW | 2023 | Spain | U.S. | RoW | 2022 | Spain | U.S. | RoW |
| Scope 1 | 106,289 | 33.2% | 59.6% | 7.2% | 106,459 | 31.5% | 60.3% | 8.2% | 95,242 | 30.4% | 61.9% | 7.7% |
| Scope 2 (Location-based) | 84,343 | 18.6% | 68.9% | 12.6% | 136,237 | 11.3% | 80.6% | 8.1% | 105,068 | 9.3% | 83.5% | 7.3% |
| Scope 2 (Market-based) | 73,876 | 15.0% | 69.9% | 15.1% | 98,106 | 106,545 | ||||||
| Scope 3 | 1,051,606 | 24.1% | 51.8% | 24.2% | 947,463 | 22.8% | 53.0% | 16.7% | 1,416,451 | 16.9% | 64.4% | 18.8% |
| EMISSIONS BIOTEST | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| % | 2024 | Germany | RoW | 2023 | Germany | Spain | U.S. | RoW | 2022 Germany | Spain | U.S. | RoW | |
| Scope 1 | 16,935 | 96.2% | 3.8% | 18,300 | 94.7% | 0.0% | 0.0% | 5.3% | 12,283 | 99.4% | 0.0% | 0.0% | 0.6% |
| Scope 2 (Market-based) | 25,092 | 95.6% | 4.4% | 15,464 | 90.3% | 0.0% | 0.0% | 9.7% | 6,523 | 94.8% | 3.1% | 0.0% | 2.1% |
| Scope 3 | 92,215 | 81.5% | 18.5% | NA* | NA* | NA* | NA* | NA* | NA* | NA* | NA* | NA* | NA* |
*NA: Not available
| Retrospective | Targets | |||||
|---|---|---|---|---|---|---|
| 2024 | 2023 | Annual variation (%) |
2022 (base year) |
2025 | 2030 | Progreso (%) |
| 106,289 | 106,459 | -0.2% | 95,242 | ** | **** | * |
| NAP* | NAP* | NAP* | NAP* | NAP* | NAP* | NAP* |
| 84,343 | 136,237 | -38.1% | 105,068 | NAP* | NAP* | NAP* |
| 73,876 | 98,106 | -24.7% | 106,546 | ** | **** | * |
| 1,051,606 | 947,463 | 11.0% | 1,416,451 | - | 1,062,338 | -25.76 |
| 556,590 | 546,309 | 1.9% | 765,443 | *** | 597,046 | -27.29 |
| 85,748 | 86,084 | -0.4% | 198,034 | *** | 154,467 | -56.70 |
| 49,775 | 54,536 | -8.7% | 56,971 | *** | 2,848.55 | -12.63 |
| 275,620 | 156,333 | 76.3% | 216,062 | *** | 172,849.6 | 27.57 |
| 11,229 | 10,814 | 3.8% | 7,021 | NAP* | NAP* | NAP* |
| 16,379 | 20,432 | -19.8% | 22,780 | NAP* | NAP* | NAP* |
| 34,227 | 37,810 | -9.5% | 40,637 | NAP* | NAP* | NAP* |
| 3,414 | 16,119 | -78.8% | 21,860 | NAP* | NAP* | NAP* |
| Not relevant | Not relevant | NAP* | Not relevant | NAP* | NAP* | NAP* |
| Not relevant | Not relevant | NAP* | Not relevant | NAP* | NAP* | NAP* |
| 2,506 | 3,544 | -29.3% | 2,936 | NAP* | NAP* | NAP* |
| 6,671 | 6,278 | 6.3% | 4,065 | NAP* | NAP* | NAP* |
| Not relevant | Not relevant | NAP* | Not relevant | NAP* | NAP* | NAP* |
| Not relevant | Not relevant | NAP* | Not relevant | NAP* | NAP* | NAP* |
| 9,449 | 9,205 | 2.7% | 80,643 | NAP* | NAP* | NAP* |
| 1,242,238 | 1,190,159 | 4.4% | 1,616,761 | NAP* | NAP* | NAP* |
| 1,231,771 | 1,152,027 | 6.9% | 1,618,240 | NAP* | NAP* | NAP* |
* NAP: Not applicable
** The target was set for Scope 1 and 2 combined. For 2025, this corresponds to a 7% reduction in Scope 1 and 2 emissions. In 2022 (base year), total Scope 1 and 2 emissions (market-based) were 201,788 tCO2e. To meet the 7% reduction target in 2025, emissions must reach 187,662 tCO2e.
*** A transition plan is in progress to develop specific measures to achieve annual reductions. The reduction target has been set for 2030, not annually.
**** The target was set for Scope 1 and 2 combined. By 2030, achieve a 42% reduction in Scope 1 and 2 emissions. In 2022 (base year), total Scope 1 and 2 emissions (market-based) were 201,788 tCO2e. To meet the 42% reduction target in 2030, emissions must reach 117,037 t CO2e.
***** The current progress is a reduction of 11%.
| Retrospective | |||||
|---|---|---|---|---|---|
| t CO2 e (equivalent) | 2024 | 2023 | Annual variation (%) | 2022 | |
| Scope 1 GHG emissions | |||||
| Gross Scope 1 GHG emissions (t CO2 eq) | 16,935 | 15,210 | 11% | 18,186 | |
| Percentage of Scope 1 GHG emissions from regulated emission trading schemes (%) | 0 | 0 | NAP | 0 | |
| Scope 2 GHG emissions | |||||
| Gross location-based Scope 2 GHG emissions (t CO2 eq) | 12,431 | 11,457 | 9% | 9,183 | |
| Gross market-based Scope 2 GHG emissions (t CO2 eq) | 25,092 | 21,905 | 15% | 931 | |
| Significant scope 3 GHG emissions | |||||
| Total Gross indirect (Scope 3) GHG emissions (t CO2 eq) | 92,215 | 102,043 | -10% | 82,213 | |
| 1 Purchased goods and services | 64,218 | 50,803 | 26% | 43,892 | |
| 2 Capital goods | 9,545 | 21,089 | -55% | 10,126 | |
| 3 Fuel and energy-related Activities (not included in Scope1 or Scope 2) | 6,272 | 6,067 | 3% | 3,548 | |
| 4 Upstream transportation and distribution | 4,747 | 14,486 | -67% | 13,456 | |
| 5 Waste generated in operations | 4,866 | 4,844 | 0% | 437 | |
| 6 Business traveling | 453 | 1,893 | -76% | 1,402 | |
| 7 Employee commuting | 1,833 | 59 | 3002% | 2,531 | |
| 8 Upstream leased assets | 175 | 1,494 | -88% | 1,361 | |
| 9 Downstream transportation | 0 | 0 | 0 | ||
| 10 Processing of sold products | 0 | 0 | 0 | ||
| 11 Use of sold products | 0 | 328 | -100% | 183 | |
| 12 End-of-life treatment of sold products | 6 | 582 | -99% | 253 | |
| 13 Downstream leased assets | 0 | 0 | 0 | ||
| 14 Franchises | 0 | 0 | 0 | ||
| 15 Investments | 100 | 398 | -75% | 5,022 | |
| Total GHG emissions | |||||
| Total GHG emissions (locationbased) (t CO2 eq) | 121,581 | 128,709 | -6% | 1,616,761 | |
| Total GHG emissions (marketbased) (t CO2 eq) | 134,242 | 139,158 | -4% | 1,618,240 |
* Biotest has not yet set any emissions reduction targets.
| REFRIGERANT GAS LEAKS | REFRIGERANT GAS LEAKS - BIOTEST | ||||
|---|---|---|---|---|---|
| Absolute value (T) | 2024 | 2023 | 2022 | Absolute value (T) | 2024 |
| HCFC | 0.06 | 0.44 | 0.23 | HCFC | 0.00 |
| HFC | 3.68 | 3.08 | 4.06 | HFC | 1.06 |
| Others | 0.00 | 0.03 | 0.02 | Others * | 0.03 |
| GHG EMISSIONS INTENSITY | ||||||||
|---|---|---|---|---|---|---|---|---|
| T/CO2e/million euros | 2024 | 2023 | 2022 | |||||
| Total Grifols (Location-based) |
184.89 | 195.46 | 283.51 | |||||
| Total Grifols (Market-based) |
183.33 | 189.20 | 283.77 |
| REFRIGERANT GAS LEAKS | REFRIGERANT GAS LEAKS - BIOTEST | |||||
|---|---|---|---|---|---|---|
| Absolute value (T) | 2024 | 2023 | 2022 | Absolute value (T) | 2024 | 2023 |
| HCFC | 0.06 | 0.44 | 0.23 | HCFC | 0.00 | 0.00 |
| HFC | 3.68 | 3.08 | 4.06 | HFC | 1.06 | 0.73 |
| Others | 0.00 | 0.03 | 0.02 | Others * | 0.03 | 1.63 |
*Includes natural refrigerants R744 CO2 and R290 Propan
| GHG EMISSIONS INTENSITY - BIOTEST | ||
|---|---|---|
| T/CO2e/million euros | 2024 | |
| Total Biotest (Location-based) | 167.41 | |
| Total Biotest (Market-based) | 184.85 |
| GRIFOLS | |
|---|---|
| --------- | -- |
| GHG EMISSIONS INTENSITY SCOPE 1+2 | ||||
|---|---|---|---|---|
| T/CO2e/million euros | 2024 | 2023 | 2022 | |
| Total Grifols (Location-based) |
28.37 | 39.86 | 35.13 | |
| Total Grifols (Market-based) |
26.82 | 33.60 | 35.38 |
| GHG EMISSIONS RELATED TO TRANSPORT | ||||
|---|---|---|---|---|
| 2024 | 2023 | 2022 | ||
| CO2 transportation emissions (t CO2 ) |
330,177 | 214,575 | 279,478 | |
| CO2 transportation emissions / sales (t CO2 / M €) |
49.14 | 37.63 | 49.01 |
*Emissions from container transport, employee commuting and business travel have been considered.
| T/CO2e/million euros | 2024 |
|---|---|
| Total Biotest (Location-based) | 40.44 |
| Total Biotest (Market-based) | 57.87 |
GHG EMISSIONS INTENSITY SCOPE 1+2 - BIOTEST
| GHG EMISSIONS RELATED TO TRANSPORT - BIOTEST | ||
|---|---|---|
| 2024 | ||
| CO2 transportation emissions (t CO2 ) |
6,586.00 | |
| CO2 transportation emissions / sales (t CO2 / M €) |
9.07 |
*Emissions from container transport, employee commuting and business travel have been considered.
| NATURAL GAS BY BUSINESS UNIT | |||
|---|---|---|---|
| kWh | 2024 | 2023 | 2022 |
| Biopharma+ Plasma Procurement | 454,501,633 | 462,235,995 | 407,296,433 |
| Diagnostic | 24,014,877 | 23,432,351 | 23,583,127 |
| Others | 21,714,451 | 22,792,328 | 21,181,198 |
| Bio Supplies | 229,672 | 363,976 | 2,989 |
| Commercial affiliates | 123,551 | 112,306 | 88,456 |
| Total | 500,584,184 | 508,936,955 | 452,152,203 |
| NATURAL GAS BY BUSINESS UNIT - BIOTEST | ||||
|---|---|---|---|---|
| kWh | 2024 | 2023 | 2022 | |
| Plasma Procurement | 22,850 | 3,751,543 | 456,548 | |
| Biopharma | 77,219,626 | 77,568,277 | 50,916,230 | |
| Total | 77,242,476 | 81,319,820 | 51,372,778 |
| NATURAL GAS BY COUNTRY | |||
|---|---|---|---|
| kWh | 2024 | 2023 | 2022 |
| Spain* | 187,309,134 | 176,029,667 | 143,376,530 |
| U.S. | 287,941,466 | 306,696,892 | 289,704,028 |
| RoW | 25,333,585 | 26,210,396 | 19,071,645 |
| Total | 500,584,185 | 508,936,955 | 452,152,203 |
*The consumption of natural gas from the cogeneration plant is included in Spain's overall totals
| NATURAL GAS BY COUNTRY - BIOTEST | ||||
|---|---|---|---|---|
| kWh | 2024 | 2023 | 2022 | |
| Germany | 77,144,416 | 78,954,414 | 51,237,535 | |
| RoW | 98,060 | 3,471,836 | 60,705 | |
| Total | 77,242,476 | 82,426,250 | 51,298,240 |
| General | Environment Climate Change |
Social | Governance | Annexes | ||
|---|---|---|---|---|---|---|
| NATURAL GAS VALUE RELATIVE TO SALES | ||||||
| kWh/million euros | 2024 | 2023 | 2022 | |||
| Biopharma+ Plasma Procurement | 80,457 | 91,438 | 87,701 | |||
| Diagnostic | 37,238 | 34,960 | 35,131 | |||
| Others | 103,782 | 112,029 | 84,669 | |||
| Bio Supplies | 1,065 | 2,275 | 20 | |||
| Commercial affiliates | NA | NA | NA | |||
| Total | 74,505 | 83,585 | 79,287 | |||
| kWh/million euros Plasma Procurement Biopharma |
NATURAL GAS VALUE RELATIVE TO SALES - BIOTEST | 2024 1,324 134,157 |
2023 91,114 176,470 |
2022 13,602 166,198 |
||
| Total | 106,361 | 267,584 | 166,198 | |||
| NATURAL GAS VALUE RELATIVE TO PRODUCTION | ||||||
| kWh/Production index | 2024 | 2023 | 2022 | |||
| Biopharma+ Plasma Procurement* | 8.5 | 8.8 | 9.2 | |||
| Diagnostic** | 37,238 | 34,960 | 35,131 | |||
| Others** | 103,782 | 112,029 | 84,669 | |||
| Bio Supplies** | 1,065 | 2,275 | 20 | |||
| Commercial affiliates | NA | NA | NA |
Production index: * Liters of plasma: fractionated + equivalent / ** Sales
| NATURAL GAS VALUE RELATIVE TO PRODUCTION - BIOTEST | |||
|---|---|---|---|
| kWh/Production index | 2024 | 2023 | 2022 |
| Plasma Procurement** | 0.04 | 6.5 | 1.0 |
| Biopharma* | 25 | 42 | 154 |
Total 74,505 83,585 79,287
Production index: * Liters of plasma: fractionated + equivalent / ** Sales
| FOSSIL FUEL CONSUMPTION | ||
|---|---|---|
| kWh | 2024 | 2023 |
| Diesel* | 3,333,981 | 4,052,948 |
| Gasoline** | 299,998 | 228,749 |
| Propane*** | 675,054 | 392,800 |
| Natural gas**** | 500,584,185 | 508,936,955 |
| Total | 504,893,218 | 513,611,452 |
*Conversion factor: liters to kWh = 9.94
**Conversion factor: liters to kWh = 9.19
***Conversion factor: liters to kWh = 6.70
****Includes natural gas used in the cogeneration plant
| FOSSIL FUEL CONSUMPTION – BIOTEST* | ||
|---|---|---|
| kWh | 2024 | 2023 |
| Diesel** | 972,356 | 336,846 |
| Gasoline*** | 123,741 | 269,654 |
| Natural gas**** | 77,242,476 | 78,181,246 |
| Total | 78,338,573 | 78,787,746 |
*Conversion factor: liters to kWh = 9.94
**Conversion factor: liters to kWh = 9.19
***Conversion factor: liters to kWh = 6.70
****Includes natural gas used in the cogeneration plant
| kWh | 2024 |
|---|---|
| Biogas** | 101,995 |
| Total | 101,995 |
*Grifols does not consume renewable fuels from biomass, biofuels or hydrogen.
**The biogas consumed by Grifols is produced at one of its own wastewater treatment plants in Spain and is used internally as boiler fuel.
*Biotest does not consume renewable fuels such as biomass, biofuels or hydrogen.
| 2024 | 2023 | 2022 |
|---|---|---|
| 380,344,448 | 395,449,664 | 399,690,586 |
| 27,102,724 | 27,076,568 | 28,799,845 |
| 2,047,710 | 2,560,933 | 545,997 |
| 16,915,870 | 17,130,922 | 17,863,379 |
| 3,172,283 | 3,121,378 | 3,776,145 |
| 429,583,035 | 445,339,465 | 450,675,952 |
| ELECTRICITY BY BUSINESS UNIT - BIOTEST | |||
|---|---|---|---|
| kWh | 2024 | 2023 | 2022 |
| Plasma Procurement | 3,568,485 | 3,206,163 | 2,074,670 |
| Biopharma | 32,492,284 | 31,391,544 | 21,388,628 |
| Total | 36,060,769 | 34,597,707 | 23,463,298 |
| ELECTRICITY BY COUNTRY | |||
|---|---|---|---|
| kWh | 2024 | 2023 | 2022 |
| Spain | 92,996,130 | 94,846,417 | 92,681,455 |
| U.S. | 299,186,028 | 312,804,351 | 321,130,633 |
| RoW | 37,400,878 | 37,688,697 | 36,863,865 |
| Total | 429,583,036 | 445,339,465 | 450,675,952 |
| ELECTRICITY BY COUNTRY - BIOTEST | |||
|---|---|---|---|
| kWh | 2024 | 2023 | 2022 |
| Germany | 33,479,994 | 32,250,734 | 22,279,317 |
| RoW | 2,580,775 | 2,301,682 | 1,162,798 |
| Total | 36,060,769 | 34,552,416 | 23,442,115 |
| ELECTRICITY VALUE RELATIVE TO SALES | ||||
|---|---|---|---|---|
| kWh/million euros | 2024 | 2023 | 2022 | |
| Biopharma+Plasma Procurement | 67,329 | 78,226 | 86,063 | |
| Diagnostic | 42,026 | 40,396 | 42,902 | |
| Bio Supplies | 9,495 | 16,010 | 3,738 | |
| Others | 80,847 | 84,202 | 71,406 | |
| Commercial affiliates | NA | NA | NA | |
| Total | 63,937 | 73,140 | 79,028 |
| General | Environment Climate Change |
Social | Governance | Annexes | |
|---|---|---|---|---|---|
| ELECTRICITY VALUE RELATIVE TO SALES - BIOTEST |
| Total | 49,655 | 147,655 | 131,725 |
|---|---|---|---|
| Biopharma | 56,450 | 70,156 | 69,816 |
| Plasma Procurement | 206,726 | 77,499 | 61,812 |
| kWh/million euros | 2024 | 2023 | 2022 |
| ELECTRICITY VALUE RELATIVE TO PRODUCTION | ||||
|---|---|---|---|---|
| kWh/Production index | 2024 | 2023 | 2022 | |
| Biopharma+Plasma Procurement* | 7.1 | 7.5 | 9.0 | |
| Diagnostic** | 42,026 | 40,396 | 42,902 | |
| Bio Supplies** | 9,495 | 16,010 | 3,738 | |
| Others** | 80,847 | 84,202 | 71,406 | |
| Commercial affiliates | NAP | NAP | NAP |
Production index: * Liters of plasma: fractionated + equivalent / ** Sales
| ELECTRICITY VALUE RELATIVE TO PRODUCTION - BIOTEST | ||||
|---|---|---|---|---|
| kWh/Production index | 2024 | 2023 | 2022 | |
| Plasma Procurement** | 5.7 | 5.6 | 6.3 | |
| Biopharma* | 10 | 17 | 19 |
Production index: * Liters of plasma: fractionated + equivalent / ** Sales
| RENEWABLE ELECTRICITY CONSUMPTION BY COUNTRY | |||
|---|---|---|---|
| kWh | 2024 | 2023 | |
| Spain | 50,285,624 | 20,727,346 | |
| U.S. | 132,000,000 | 119,999,113 | |
| RoW | 9,457,281 | 11,869,794 | |
| Total | 191,742,905 | 152,596,253 |
| RENEWABLE ELECTRICITY CONSUMPTION BY COUNTRY – BIOTEST | ||
|---|---|---|
| kWh | 2024 | |
| Germany | 266,092 | |
| RoW | 32,758 | |
| Total | 298,850 |
| RENEWABLE ELECTRICITY CONSUMPTION BY SOURCE | |||
|---|---|---|---|
| kWh | 2024 | 2023 | |
| PPA (Power Purchase Agreements) | 18,856,596 | 20,273,875 | |
| Guarantees of origin | 172,468,896 | 131,868,907 | |
| Self-generated (onsite solar photovoltaic) | 417,413 | 453,471 | |
| Total | 191,742,905 | 152,596,253 |
| RENEWABLE ELECTRICITY CONSUMPTION BY SOURCE – BIOTEST | ||
|---|---|---|
| kWh | 2024 | |
| PPA (Power Purchase Agreements) | 0 | |
| Guarantees of origin | 32,758 | |
| Self-generated (onsite solar photovoltaic) | 266,092 | |
| Total | 298,850 |
| General | Environment | Social | Governance | Annexes | |
|---|---|---|---|---|---|
| Climate Change |
| SELF-GENERATED AND SELF-CONSUMED ELECTRICITY BY BUSINESS UNIT | |||
|---|---|---|---|
| kWh | 2024 | 2023 | |
| Biopharma+Plasma procurement | 292,551 | 290,659 | |
| Diagnostic | 0 | 0 | |
| Bio Supplies | 0 | 0 | |
| Others | 124,862 | 162,812 | |
| Commercial affiliates | 0 | 0 | |
| Total | 417,413 | 453,471 |
| SELF-GENERATED AND SELF-CONSUMED ELECTRICITY BY BUSINESS UNIT - BIOTEST | ||
|---|---|---|
| kWh | 2024 | |
| Plasma Procurement | 0 | |
| Biopharma | 266,092 | |
| Total | 266,092 |
| RENEWABLE AND NON-RENEWABLE ELECTRICITY PRODUCTION | ||
|---|---|---|
| kWh | 2024 | 2023 |
| Self-generated and self-consumed renewable electricity (solar PV) | 417,413 | 453,471 |
| Self-generated non-renewable electricity (cogeneration) | 43,395,980 | 40,656,130 |
| PURCHASED OR ACQUIRED RENEWABLE* ELECTRICITY, HEAT, STEAM AND COOLING | |||
|---|---|---|---|
| kWh | 2024 | 2023 | 2022 |
| Electricity | 191,742,905 | 152,596,253 | 118,766,313 |
*Grifols does not purchase or acquire renewable heat, steam or cooling
| PURCHASED OR ACQUIRED RENEWABLE ELECTRICITY, HEAT, STEAM AND COOLING– BIOTEST | ||
|---|---|---|
| kWh | 2024 | |
| Electricity | 298,850 |
*Biotest does not purchase or acquire renewable heat, steam or cooling
| kWh | 2024 | 2023 | 2022 |
|---|---|---|---|
| Biopharma+Plasma procurement | 805,503,399 | 831,629,897 | 794,588,340 |
| Diagnostic | 51,176,144 | 50,553,569 | 52,435,934 |
| Bio Supplies | 2,280,994 | 2,925,893 | 549,477 |
| Others | 38,777,951 | 39,970,526 | 39,044,577 |
| Commercial affiliates | 3,676,342 | 3,679,067 | 3,871,545 |
| Total | 901,414,830 | 928,758,952 | 890,489,873 |
| kWh | 2024 | 2023 | 2022 |
|---|---|---|---|
| Plasma Procurement | 4,507,530 | 6,957,706 | 2,572,197 |
| Biopharma | 104,687,422 | 109,255,786 | 72,897,207 |
| Total | 109,194,952 | 116,213,492 | 75,469,404 |
| General | Environment | Social | Governance | Annexes | |
|---|---|---|---|---|---|
| Climate Change |
| CONSUMPTION VALUE RELATIVE TO SALES | |||
|---|---|---|---|
| kWh | 2024 | 2023 | 2022 |
| Biopharma+Plasma procurement | 142,592 | 164,510 | 171,095 |
| Diagnostic | 79,355 | 75,423 | 78,112 |
| Bio Supplies | 10,577 | 18,292 | 3,762 |
| Others | 185,335 | 196,463 | 156,075 |
| Commercial affiliates | NA | NA | NA |
| Total | 134,710 | 152,534 | 156,152 |
| CONSUMPTION VALUE RELATIVE TO SALES - BIOTEST | |||
|---|---|---|---|
| kWh | 2024 | 2023 | 2022 |
| Plasma Procurement | 261,126 | 168,628 | 76,635 |
| Biopharma | 181,878 | 247,290 | 237,947 |
| Total | 150,359 | 415,918 | 314,582 |
| COGENERATION PLANT | |||
|---|---|---|---|
| kWh | 2024 | 2023 | 2022 |
| Natural gas consumed (kwh) | 118,347,327 | 110,159,693 | 75,119,463 |
| Total electricity generate (kwh) | 43,395,980 | 40,656,130 | 27,618,042 |
| Useful heat recoverd (kwh) | 33,624,710 | 30,387,110 | 20,623,619 |
| COGENERATION PLANT - BIOTEST | |||
|---|---|---|---|
| kWh | 2024 | 2023 | 2022 |
| Natural gas consumed (kwh) | 16,273,981 | 17,440,542 | 13,199,091 |
| Total electricity generate (kwh) | 5,637,840 | 5,958,345 | 4,770,118 |
| Useful heat recoverd (kwh) | 8,019,376 | 9,174,840 | 6,759,322 |
| 2024 2023 |
||||||
|---|---|---|---|---|---|---|
| kWh | Self-generated renewable energy* |
Renewable fuel consumption |
Purchased renewable energy** |
Self-generated renewable energy* |
Renewable fuel consumption |
Purchased renewable energy** |
| Biopharma+Plasma procurement | 292,551 | 101,995 | 169,114,734 | 290,659 | 0 | 141,796,669 |
| Diagnostic | 0 | 0 | 12,738,392 | 0 | 0 | 10,006,113 |
| Bio Supplies | 0 | 0 | 0 | 0 | 0 | 0 |
| Others | 124,862 | 0 | 8,460,751 | 162,812 | 0 | 0 |
| Commercial affiliates | 0 | 0 | 1,011,615 | 0 | 0 | 340,000 |
| Total | 417,413 | 101,995 | 191,325,492 | 453,471 | 0 | 152,142,782 |
*Not used as fuel (solar PV)
** Includes electricity, heat, steam and cooling
| 2024 | ||||
|---|---|---|---|---|
| kWh | Self-generated renewable energy* | Renewable fuel consumption | Purchased renewable energy** | |
| Plasma Procurement | 0 | 0 | 0 | |
| Biopharma | 266,092 | 0 | 32,758 | |
| Total | 266,092 | 0 | 32,758 |
*Not used as fuel (solar PV)
** Includes electricity, heat, steam and cooling
Grifols recognizes that air, water and soil pollution have an impact on human health and ecosystems, and contribute to climate change. The company identifies, manages and reports on pollutants generated by its operations that could affect air, water and soil quality.
Grifols identifies, analyzes and manages all pollution metrics related to air, water and soil. However, given its business model and value chain, water pollution is the most relevant due to its potential negative impact and associated risk to the business. The company's operations do not significantly contribute to air or soil pollution, and no material risks or opportunities have been identified in these areas.
| E2 POLLUTION |
|||
|---|---|---|---|
| Material IROs | Typology | Description | |
| WATER POLLUTION | |||
| Alteration and/or degradation of water quality |
- OO SP |
Wastewater from this sector may contain pollutants that impact the environment, which is why its proper treatment is crucial for Grifols. The company invests in solutions to improve the quality of discharged water at its main production facilities. |
|
| Non-compliance with legal requirements |
R | This environmental impact has led to stricter regulations to protect water resources and public health. Grifols works to ensure compliance with all applicable legislation on wastewater quality. Risk |
|
| + Positive impact - Negative impact R Risk OO Own Operation SP Supply Chain |
| Material Sub-Topic | Policies | Actions | Metrics and Targets |
|---|---|---|---|
| WATER POLLUTION |
• Environmental Policy • Sustainability Policy • Biodiversity Policy |
• Diverting the distillate from PEG/sorbitol evaporators to the biological treatment plan • Sending wastewater from cleaning processes to the biological treatment plan • Directing alcohol tower residues to the anaerobic treatment plant before final discharge |
Under the 2023-2026 Environmental Program • Reduce chemical oxygen demand (COD) in discharged wastewater by 240 mg/L, equivalent to an annual reduction of 123 tons. |
More information and details on Grifols' emissions that may impact air quality and/or air pollution: Section 1 on Climate Change- ESRS E1.
More information and details on water management at Grifols: Section 3 on Water Resources-ESRS E3.
More information and details on waste that may affect soil quality and/or soil pollution: Section 5 on Resource Use and Circular Economy-ESRS E5.
Pollution
Grifols has established a clear framework for pollution management through various policies that explicitly address contamination.
The Environmental Policy defines efficient water cycle management as a core principle, with a focus on minimizing water consumption, reusing water where possible, treating it to optimal levels before discharge into public sanitation systems, and prioritizing improvements in water-stressed regions.
The Sustainability Policy includes objectives focused on pollution prevention techniques to mitigate environmental risks related to Grifols' activities, taking into account the effects of climate change.
The Biodiversity Policy emphasizes improving water management as a key objective. It focuses on enhancing the quality of discharged water, incorporating water-saving measures into the design of new facilities and implementing solutions in existing ones.
In compliance with ISO 14001, Grifols integrates eco-efficiency measures into new product development (R&D), building design and engineering projects. As part of its internal standards, every project and product development process must undergo an eco-efficiency assessment to identify opportunities for reducing environmental impact. This approach also extends to pollution management. Before launching a new project, Grifols conducts an early-stage analysis to determine whether additional regulatory licenses, permit modifications, specific authorizations or pollution mitigation investments (for air, water and soil) are needed.
The company has also established recommendations for wastewater management in engineering projects. These include installing agitators and wastewater neutralization systems; prioritizing the use of CO2 over chemicals for wastewater neutralization whenever feasible; installing wastewater volume meters and where necessary, implementing more complex treatment systems.
For existing facilities, Grifols invests in necessary upgrades based on the Best Available Techniques (BAT), ensuring they are applicable to both the sector and the specific facility.
Water pollution is a key focus area of the 2023-2026 Environmental Program, which sets specific targets and initiatives to address it. Grifols continuously evaluates and monitors progress toward achieving the objectives outlined in its environmental programs.
Reduce wastewater discharge metrics
Lower chemical oxygen demand (COD) levels in wastewater at Biopharma division facilities in Barcelona by 240 mg/L by treating more high-organic-load effluents in the biological treatment plant.


Pollution
Grifols identifies, classifies, manages and reports on pollutants generated by its operations that may impact water quality.

is discharged into the sewers


being discharged
-11% COD discharge -76% suspended solids discharge
En 2024, 2.5 million m3 of wastewater was discharged to public sewers. In U.S. plants, stormwater is conveyed to public waterways including the Los Angeles River, Neuse River and San Francisco Bay. Approximately 31% of water on average is consumed in auxiliary processes such as cooling towers or incorporated into the product, while 69% is discharged to the sewer.
In 2024, the Barcelona and Clayton (North Carolina) facilities treated 908,700 m3 of wastewater using biological systems prior to discharge, representing 37% of the total discharge. Projects are underway to expand these treatments at both plants and in 2023, the new Clayton and Barcelona wastewater plants came into operation.
In water-stressed areas, the distribution of discharges corresponds to water consumption, with no significant variations from previous years.
Grifols identifies and classifies its potential water pollutants, with the most significant impact occurring at manufacturing plants. The key wastewater metric is chemical oxygen demand (COD), defined as the amount of organic and inorganic matter susceptible to oxidation.
Grifols discharges wastewater into public sewage systems, which undergo municipal treatment processes. Additionally, the main production plants of the Biopharma business unit in Barcelona and Clayton operate on-site wastewater treatment plants to reduce COD levels before discharge.
In 2024, 2,411 tons of COD were discharged, most of which corresponded to Biopharma's production facilities. In addition, 78.17 tons of suspended solids in total and 31.3 tons of nitrogen were discharged.
Grifols recognizes that microplastics can accumulate in nature due to their resistance to degradation and environmental persistence. However, this is not considered a material aspect for the organization since its operations do not generate significant direct microplastic emissions.
Grifols continues to optimize its processes to reduce plastic use wherever possible.
Nitrogen and phosphorus levels in wastewater are not considered significant substances of concern, as they primarily come from sanitary (non-industrial) discharges rather than production processes.
Grifols does not work with genetically modified organisms (GMOs) nor products that generate persistent organic pollutants (POPs). In consequence, no such discharges are produced.
The Diagnostic business unit, which accounts for approximately 10% of Grifols' revenue, uses certain substances classified as Substances of Very High Concern (SVHC) in the manufacture of some Procleix™ assays, sourced exclusively from qualified suppliers. The substances present at concentrations above 0.1% w/w (weight by weight) include:
These compounds are commonly used in the pharmaceutical industry. Any residual waste classified as hazardous under applicable regulations is collected and disposed of using designated containers, in full compliance with internal procedures and hazardous waste management regulations.
Diagnostic Grifols, as the authorized representative of GDS in the EU, notified the use of these SVHCs in the SCIP database in October 2023.
Grifols complies with all applicable national and local regulations and permits governing the disposal and treatment of wastewater from its facilities. In 2024, the company did not receive any fines related to adverse environmental impacts, including those associated with wastewater and discharges. Since no reported water pollution incidents occurred in 2024, there were no associated costs for remediation, damage compensation or legal claims.
Grifols does not discharge wastewater into natural water bodies. Instead, all wastewater is directed to local sewage systems, where it undergoes municipal or regional treatment.
Industrial plants apply necessary pre-treatment processes before final discharge. All production facilities operate in areas where local authorities regulate wastewater discharges. Production sites with an implemented and/ or certified environmental management system follow strict procedures for wastewater quality monitoring, prevention and control. Commercial offices and warehouses discharge sanitary wastewater into municipal sewage systems.
The Biopharma facilities in Barcelona operate an anaerobic wastewater treatment plant equipped with UASB (Upflow Anaerobic Sludge Bed Reactor) technology, also known as a sludge bed reactor. This highefficiency treatment process removes 85% of the organic pollutant load in oxygen-free conditions, requiring minimal energy consumption while generating biogas of renewable origin. Once treated, this biogas is used as fuel for the plant's steam production boilers, thus reducing natural gas consumption and CO2 e emissions into the atmosphere. In 2024, a total of 101,995 kWh of biogas was generated and used in the boilers.
The facility is designed to accommodate increased production, helping to lower current discharge metrics and maintain compliance as production scales up.
The Biopharma facilities in North Carolina operate a wastewater treatment plant with a processing capacity of up to 5,678 m³ per day. The largest treatment plant in Grifols' global network, this facility reduces the organic load levels of treated water to 250 mg per liter, equivalent to that of household wastewater. Today, with this highly efficient plant in operation, the water treated by Grifols contains only 32 mg of organic load per liter, well below the permitted limit.
The Los Angeles, San Francisco, and Canada facilities operate with neutralization systems before final discharge.
These facilities combined process 37% of Grifols' total wastewater discharge.
| SUSPENDED SOLIDS DISCHARGED | |||
|---|---|---|---|
| 2024 | 2023 | 2022 | |
| Total (T) | 78 | 326 | 357 |
| Relative to sales (T/million euros) | 0.00 | 0.05 | 0.06 |
| SUSPENDED SOLIDS DISCHARGED - BIOTEST | |||
| 2024 | |||
| Total (T) | 4.60 | ||
| Relative to sales (T/million euros) | 0.00 |
| General | Environment | Social | Governance | Annexes | |
|---|---|---|---|---|---|
| Pollution | |||||
| COD DISCHARGED | |||||
|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | |||
| Total (T) | 2,479 | 2,168 | 2,525 | ||
| Relative to sales (T/million euros) | 0.01 | 0.36 | 0.44 |
| 2024 | |
|---|---|
| Total (T) | 244 |
| Relative to sales (T/million euros) | 0.00 |
| 2024 | |
|---|---|
| Total (T) | 31.31 |
| Relative to sales (T/million euros) | 0.00 |
| 2024 | |
|---|---|
| Total (T) | 18.40 |
| Relative to sales (T/million euros) | 0.04 |
| OTHER EMISSIONS | |||
|---|---|---|---|
| Absolute value (T) | 2024 | 2023 | 2022 |
| NOx | 71.31 | 71.5 | 59.31 |
| CO | 64.78 | 62.7 | 63.65 |
| SO2 | 0.54 | 0.57 | 0.63 |
| OTHER EMISSIONS - BIOTEST | ||
|---|---|---|
| Absolute value (T) | 2024 | |
| NOx | NA | |
| CO | NA | |
| SO2 | NA | |
| CO EMISSIONS INTENSITY | |||
|---|---|---|---|
| T/CO/million euros | 2024 | 2023 | 2022 |
| Total Grifols | 0.01 | 0.01 | 0.01 |
| SO2 EMISSIONS INTENSITY | |||
|---|---|---|---|
| T/SO2/million euros | 2024 | 2023 | 2022 |
| Total Grifols | 0.00 | 0.00 | 0.00 |
| NOX EMISSIONS INTENSITY | |||
|---|---|---|---|
| T/NOX/million euros | 2024 | 2023 | 2022 |
| Total Grifols | 0.01 | 0.01 | 0.01 |
Grifols' activities do not have a direct impact on the blue economy or marine resources. However, water plays a crucial role throughout the entire production process of plasma-derived medicines, both in core production and auxiliary processes. Additionally, strict quality water standards are applied to ensure the sterility of Grifols' products.
In 2024, following international guidelines, Grifols reported data on water withdrawal, consumption and discharge. In general terms, water withdrawal refers to all water extracted from surface, groundwater or thirdparty sources, regardless of how it is used throughout the year. In contrast, water consumption accounts for the portion of withdrawn water that does not return to the system, either because it is incorporated into the product/ process or lost through evaporation.
This means that not all withdrawn water is consumed. A portion is used and consumed, while another is returned to natural systems as discharge, though its quality or characteristics may have changed.
Grifols implements practices to minimize the water footprint of its activities and promotes water management based on circular economy principles.
| E3 WATER RESOURCES |
|||
|---|---|---|---|
| Material IROs | Typology | Description | |
| WATER | |||
| Contribution to water stress | - OO SP |
Like many industries, the pharmaceutical sector depends on water resources for its operations. Effective water management is crucial to reducing environmental impact and ensuring long-term sustainability. |
|
| Reduced water availability | R | As outlined in the Climate Risk and Opportunity Analysis, potential increases in operational costs and production disruptions due to water scarcity, declining water quality or stricter water use regulations represent a material risk for Grifols. |
|
| + Positive impact - Negative impact R Risk OO Own Operation SP Supply Chain |
More information on water discharge-related IROs: "Pollution section-ESRS E2".
| Material Sub-Topic | Policies | Actions | Metrics and Targets |
|---|---|---|---|
| Water | • Sustainability Policy • Environmental Policy • Biodiversity Policy |
• Recovering clean water from production processes for reuse in auxiliary operations • Reducing water consumption in reactor cleaning • Minimizing water use in treatment systems such as reverse osmosis • Lowering the frequency of washing plasma bottle containers by using biodegradable soap |
Under the 2023-2026 Corporate Environmental Program: • Reduce water withdrawal by 85,737 m3 per year*. |
*The term "consumption" has been replaced with "withdrawal" in accordance with international guidelines.
For more information and details on the management of discharges and wastewater that may impact water quality, see Section 2 on Pollution – ESRS E2.
General Environment Social Governance Annexes Water resources
Grifols is developing a specific policy to address all aspects related to water withdrawal, consumption and management. However, several existing policies already define the principles, guidelines and strategies the company follows to ensure the sustainable use of water resources.
The Sustainability Policy recognizes water as a critical resource due to its role in production processes and its impact on product quality. Grifols is committed to efficient water use and minimizing environmental impact through initiatives such as optimizing water consumption in production plants, recycling and reusing water wherever possible, and managing water resources sustainably. Additionally, the company works to implement practices that preserve water sources long-term, reducing its water footprint.
The Environmental Policy sets out key principles and commitments related to water management, including sustainable water use; minimizing water-related environmental impact; monitoring and controlling water usage to comply with environmental regulations; conserving aquatic ecosystems and biodiversity; educating and training employees on sustainable practices
Grifols' Biodiversity Policy recognizes water as essential to life and ecosystem balance. It includes commitments to sustainable water management, safeguarding water quality and collaborating with communities and international organizations to protect aquatic ecosystems and biodiversity.
Water is a key area of focus in Grifols' 2023-2026 Corporate Environmental Program, which sets specific objectives aimed at optimizing and reducing water consumption. The company continuously evaluates and monitors progress toward the targets outlined in its environmental programs.
| DEGREE OF COMPLIANCE WITH ACTIONS AT YEAR END 2024 | 80% | |
|---|---|---|
| Water resource objectives | ||
| Reduce water withdrawal for auxiliary processes, | ||
| Reduce annual water withdrawal by more than 85,000 m3 |
Annual reduction of more than 46,000 m3. | |
| Reduce water rejection from water treatment for production. | ||
| Annual reduction of more than 39,000 m3. |

General Environment Social Governance Annexes Water resources
Water withdrawal refers to all water extracted from natural sources or thirdparty suppliers, regardless of how it is used. Water consumption refers to the portion of withdrawn water that does not return to the environment because it evaporates, is incorporated into products or is lost in processes. Not all withdrawn water is consumed; some is returned to the system as discharge, though its quality may be altered.
Grifols operates in geographical regions where water withdrawal control is essential, including California (U.S.) and Catalonia and Murcia (Spain).
In 2024, 19.7% of total water withdrawal occurred in water-stressed areas, maintaining levels similar to previous years.
For this reason, optimizing water use is essential to Grifols, especially as the company expands its industrial activity.
Grifols does not use surface freshwater (from rivers, wetlands, etc.), brackish surface water (seawater), non-renewable groundwater or produced/infiltrated water. Instead, 90.6% of the water used comes from public supply networks, while 9.4% is sourced from on-site wells at its Barcelona facilities, which supply water for production processes. The company ensures sustainable management of these resources, preventing any negative impact on local water availability and fully complying with applicable environmental regulations.
Water withdrawals from on-site wells are conducted in accordance with permits issued by the relevant water authority, which regulates all authorizations and water usage. Grifols monitors these withdrawals to ensure they remain within approved limits.
Grifols does not store water for purposes other than fire protection systems, located at production sites in Spain and Ireland, with a total storage capacity of 2,564 m³.
In 2024, water consumption totaled 1.1 million m3 , reflecting a 11.3% absolute reduction. By business unit, Biopharma and Plasma Procurement, which together account for 92% of total water use, maintained stable withdrawal levels.
In 2024 Grifols was awarded a B-rating by the Carbon Disclosure Project (CDP) Water Security.
of production facilities have implemented water-saving measures
of withdrawn water is returned to the natural system
3.6 M m3 -2% vs 2023 26% Spain • 68% U.S. • 6% RoW
-11% vs 2023 20% Spain • 76% U.S. • 4% RoW
2.5 M m3 +2% vs 2023
28% Spain • 64% U.S. • 8% RoW
| WATER CONSUMPTION BY BUSINESS UNIT | |||
|---|---|---|---|
| m3 | 2024 | 2023 | 2022 |
| Biopharma + Plasma Procurement | 1,014,214 | 1,144,508 | 651,895 |
| Diagnostic | 40,267 | 30,991 | 13,961 |
| Bio Supplies | 79 | 2 | 0 |
| Others | 52,114 | 72,978 | 35,830 |
| Commercial affiliates | 1,217 | 806 | 3 |
| Total | 1,107,891 | 1,249,286 | 701,689 |
The term "consumption" has been replaced with "withdrawal" in accordance with international guidelines.
*Not including Biotest.
For detailed data on water consumption, withdrawal and discharge, see the tables at the end of this chapter.
Applying circular economy principles to water management is key to ensuring sustainable and efficient use of resources. In this regard, Grifols focuses on reducing water demand by adopting advanced technologies and practices to lower usage while optimizing industrial processes to minimize withdrawal.
Grifols ensures that water-saving measures are fully integrated into the design of any new facilities and implements water efficiency measures in existing buildings. These include reducing water use in reactor and equipment cleaning by installing automated cleaning-in-place (CIP) systems and minimizing water use in treatment systems such as reverse osmosis.
The company is also firmly committed to water reuse and actively recycles clean water from production processes. On average, 31% of the water used in Grifols' operations is reused in auxiliary processes, such as outdoor cleaning and cooling towers, or is incorporated into products.
| WATER WITHDRAWAL BY BUSINESS UNIT | |||
|---|---|---|---|
| m3 | 2024 | 2023 | 2022 |
| Biopharma+Plasma procurement | 3,297,133 | 3,373,254 | 2,733,390 |
| Diagnostic | 83,531 | 68,790 | 104,641 |
| Bio Supplies | 8,480 | 12,279 | 3,363 |
| Others | 192,134 | 216,983 | 188,082 |
| Commercial affiliates | 6,079 | 5,502 | 4,878 |
| Total | 3,587,357 | 3,676,808 | 3,034,354 |
| WATER WITHDRAWAL BY BUSINESS UNIT - BIOTEST | |||
| m3 | 2024 | 2023 | 2022 |
| Plasma Procurement | 11,522 | 15,549 | 6,610 |
| Biopharma | 453,350 | 474,819 | 333,221 |
| Total | 464,872 | 490,368 | 339,831 |
| WATER WITHDRAWAL BY COUNTRY | |||
| m3 | 2024 | 2023 | 2022 |
| Spain | 929,864 | 961,208 | 884,304 |
| U.S. | 2,429,566 | 2,456,863 | 2,039,650 |
| RoW | 227,927 | 258,738 | 113,575 |
| Total | 3,587,357 | 3,676,809 | 3,037,529 |
| WATER WITHDRAWAL BY COUNTRY - BIOTEST | |||
| m3 | 2024 | 2023 | 2022 |
| Germany | 456,852 | 476,956 | 333,317 |
| RoW | 8,020 | 12,646 | 6,447 |
| Total | 464,872 | 489,602 | 339,764 |
| WATER WITHDRAWAL VALUE RELATIVE TO SALES | |||
| m3/million euros | 2024 | 2023 | 2022 |
| Biopharma+Plasma Procurement | 584 | 667 | 589 |
| Diagnostic | 130 | 103 | 156 |
| Bio Supplies | 39 | 77 | 23 |
| Others | 918 | 1,067 | 752 |
| Commercial affiliates | NA | NA | NA |
| Total | 534 | 604 | 532 |
| General | Environment | Social | Governance | Annexes | |
|---|---|---|---|---|---|
| Water resources | |||||
| WATER WITHDRAWAL VALUE RELATIVE TO SALES - BIOTEST | |||
|---|---|---|---|
| m3/million euros | 2024 | 2023 | 2022 |
| Plasma Procurement | 667 | 368 | 197 |
| Biopharma | 788 | 1,065 | 1,088 |
| Total | 640 | 1,433 | 1,382 |
| WATER WITHDRAWAL VALUE RELATIVE TO PRODUCTION | |||
|---|---|---|---|
| m3/Production index | 2024 | 2023 | 2022 |
| Biopharma+Plasma Procurement* | 0.06 | 0.06 | 0.06 |
| Diagnostic** | 130 | 103 | 156 |
| Bio Supplies** | 39 | 77 | 23 |
| Others** | 918 | 1,067 | 752 |
| Commercial affiliates | NA | NA | NA |
Production index: * Liters of plasma: fractionated + equivalent / ** Sales
| WATER WITHDRAWAL VALUE RELATIVE TO PRODUCTION - BIOTEST | |||
|---|---|---|---|
| m3/Production index | 2024 | 2023 | 2022 |
| Plasma Procurement** | 18 | 368 | 0 |
| Biopharma* | 147 | 1,065 | 1 |
Production index: * Liters of plasma: fractionated + equivalent / ** Sales
| WATER WITHDRAWAL BY SOURCE AND WATER STRESSED REGIONS - 2024 | ||||||
|---|---|---|---|---|---|---|
| m3 | Total | By source | Withdrawal water-stressed regions* | |||
| Groundwater | Third party water | Irrigation net | Absolute value (m3) | % | ||
| Biopharma + Plasma | ||||||
| Procurement | 3,297,133 | 231,376 | 3,054,669 | 11,088 | 652,833 | 19.8 |
| Diagnostic | 83,531 | 0 | 70,823 | 12,708 | 27,516 | 32.9 |
| Bio Supplies | 8,480 | 0 | 8,480 | 0 | 875 | 10.3 |
| Others | 192,134 | 104,235 | 87,899 | 0 | 68,161 | 35.5 |
| Commercial affiliates | 6,079 | 0 | 6,079 | 0 | 2,765 | 45.5 |
| Total | 3,587,357 | 335,611 | 3,227,950 | 23,796 | 752,150 | 21.0 |
* Areas with high and extremely high risk according to World Resources Institute
| m3 | Total | By source | % of consumption in water-stressed regions* | |
|---|---|---|---|---|
| Groundwater | Third party water | |||
| Biopharma + Plasma Procurement | 3,373,255 | 262,471 | 3,110,784 | 19.1 |
| Diagnostic | 68,790 | 0 | 68,790 | 17.8 |
| Bio Supplies | 12,279 | 0 | 12,279 | 54.8 |
| Others | 216,983 | 130,386 | 86,597 | 34.9 |
| Commercial affiliates | 5,502 | 0 | 5,502 | 28.8 |
| Total | 3,676,809 | 392,857 | 3,283,952 | 20.1 |
* Areas with high and extremely high risk according to World Resources Institute
| GRIFOLS | |
|---|---|
| --------- | -- |
| m3 | Total | By source | % of consumption in water-stressed regions* | |
|---|---|---|---|---|
| Groundwater | Third party water |
|||
| Biopharma + Plasma Procurement | 2,733,390 | 234,824 | 2,498,566 | 19.3 |
| Diagnostic | 104,641 | 0 | 104,641 | 24.7 |
| Bio Supplies | 3,363 | 0 | 3,363 | 100.0 |
| Others | 188,082 | 120,943 | 67,139 | 26.4 |
| Commercial affiliates | 4,878 | 0 | 4,878 | 41.0 |
| Total | 3,034,354 | 355,767 | 2,678,587 | 20.0 |
* Areas with high and extremely high risk according to World Resources Institute
* Areas with high and extremely high risk according to World Resources Institute
| m3 | Total | By source | % of consumption in water-stressed regions* | |
|---|---|---|---|---|
| Groundwater | Third party water |
|||
| Plasma Procurement | 15,896 | 0 | 15,896 | 0.0% |
| Biopharma | 473,706 | 0 | 473,706 | 0.0% |
| Total | 489,602 | 0 | 489,602 | 0.0% |
* Areas with high and extremely high risk according to World Resources Institute
| m3 | Total | By source | % of consumption in water-stressed regions* | |
|---|---|---|---|---|
| Groundwater | Third party water |
|||
| Plasma Procurement | 15,896 | 0 | 15,896 | 0.0% |
| Biopharma | 473,706 | 0 | 473,706 | 0.0% |
| Total | 489,602 | 0 | 489,602 | 0.0% |
* Areas with high and extremely high risk according to World Resources Institute
| WASTEWATER DISCHARGE BY BUSINESS UNIT - BIOTEST | ||||
|---|---|---|---|---|
| m3 | 2024 | 2023 | 2022 | |
| Plasma Procurement | 7,163 | 15,896 | 15,896 | |
| Biopharma | 452,782 | 430,754 | 430,754 | |
| Total | 459,945 | 446,650 | 446,650 |
| RIFOLS | 0 |
|---|---|
General Environment Social Governance Annexes Water resources
| m3 | By destination | By treatment | In water-stressed regions*** | ||
|---|---|---|---|---|---|
| Total (public sewer system) |
No internal treatment* |
Biological systems prior to discharge** |
Absolute value (m3) |
% | |
| Biopharma + Plasma Procurement | 2,282,919 | 1,374,218 | 908,701 | 423,707 | 19 |
| Diagnostic | 43,264 | 43,264 | 0 | 21,315 | 49 |
| Bio Supplies | 8,401 | 8,401 | 0 | 796 | 9 |
| Others | 140,020 | 140,020 | 0 | 39,861 | 28 |
| Commercial affiliates | 4,861 | 4,861 | 0 | 2,758 | 57 |
| Total | 2,479,466 | 1,570,765 | 908,701 | 488,436 | 20 |
* Wastewater discharged into the sewer system with subsequent treatment of municipal services
** Internal pretreatment processes
*** Areas with high and extremely high risk according to World Resources Institute
| m3 | By destination | By treatment | By region | |
|---|---|---|---|---|
| Total (public sewer system) |
No internal treatment* |
Biological systems prior to discharge** |
% of discharged on water-stressed regions*** |
|
| Biopharma + Plasma Procurement | 2,228,746 | 1,379,555 | 849,191 | 17.5 |
| Diagnostic | 37,799 | 37,799 | 0 | 32.3 |
| Bio Supplies | 12,277 | 12,277 | 0 | 54.8 |
| Others | 144,005 | 144,005 | 0 | 27.8 |
| Commercial affiliates | 4,696 | 4,696 | 0 | 43.4 |
| Total | 2,427,523 | 1,578,332 | 849,191 | 18.6 |
* Wastewater discharged into the sewer system with subsequent treatment of municipal services
** Internal pretreatment processes
*** Areas with high and extremely high risk according to World Resources Institute
| m3 | By destination | By treatment | By region | |
|---|---|---|---|---|
| Total (public sewer system) |
No internal treatment* |
Biological systems prior to discharge** |
% of discharged on water-stressed regions*** |
|
| Biopharma + Plasma Procurement | 2,081,495 | 1,207,603 | 873,892 | 16.6 |
| Diagnostic | 90,680 | 90,680 | 0 | 24.4 |
| Bio Supplies | 3,363 | 3,363 | 0 | 100.0 |
| Others | 152,252 | 152,252 | 0 | 6.2 |
| Commercial affiliates | 4,875 | 4,875 | 0 | 41.0 |
| Total | 2,332,665 | 1,458,773 | 873,892 | 17.8 |
* Wastewater discharged into the sewer system with subsequent treatment of municipal services
** Internal pretreatment processes
*** Areas with high and extremely high risk according to World Resources Institute
| m3 | By destination | By treatment | In water-stressed regions*** | ||
|---|---|---|---|---|---|
| Total (public sewer system) |
No internal treatment* |
Biological systems prior to discharge** |
Absolute value (m3) |
% | |
| Plasma Procurement | 7,163 | 7,163 | 0 | 0 | 0.0% |
| Biopharma | 452,782 | 365,198 | 87,584 | 0 | 0.0% |
| Total | 459,945 | 372,361 | 87,584 | 0 | 0.0% |
* Wastewater discharged into the sewer system with subsequent treatment of municipal services
** Internal pretreatment processes
*** Areas with high and extremely high risk according to World Resources Institute
| RIFOLS | 0 |
|---|---|
Water resources
| WASTEWATER DISCHARGE BY SOURCE AND STRESS AREAS - BIOTEST - 2023 | ||||
|---|---|---|---|---|
| m3 | By destination | By treatment | By region | |
| Total (public sewer system) |
No internal treatment* |
Biological systems prior to discharge** |
% of discharged on water stressed regions*** |
|
| Plasma Procurement | 15,896 | 15,896 | 0 | 0.0% |
| Biopharma | 430,754 | 430,754 | 0 | 0.0% |
| Total | 446,650 | 446,650 | 0 | 0.0% |
* Wastewater discharged into the sewer system with subsequent treatment of municipal services
** Internal pretreatment processes
*** Areas with high and extremely high risk according to World Resources Institute
| m3 | By destination | By treatment | By region | |
|---|---|---|---|---|
| Total (public sewer system) |
No internal treatment* |
Biological systems prior to discharge** |
% of discharged on water stressed regions*** |
|
| Plasma Procurement | 15,896 | 15,896 | 0 | 0.0% |
| Biopharma | 430,754 | 430,754 | 0 | 0.0% |
| Total | 446,650 | 446,650 | 0 | 0.0% |
* Wastewater discharged into the sewer system with subsequent treatment of municipal services
** Internal pretreatment processes
*** Areas with high and extremely high risk according to World Resources Institute
| m3 | 2024 | 2023 | 2022 |
|---|---|---|---|
| Biopharma + Plasma Procurement | 1,014,214 | 1,144,508 | 651,895 |
| Diagnostic | 40,267 | 30,991 | 13,961 |
| Bio Supplies | 79 | 2 | 0 |
| Others | 52,114 | 72,978 | 35,830 |
| Commercial affiliates | 1,217 | 806 | 3 |
| Total | 1,107,891 | 1,249,285 | 701,689 |
Water consumption was calculated by excluding water discharged from water withdrawn according to international standards
Water consumption was calculated by excluding water discharged from water withdrawn according to international standards
*Biotest's water consumption in water-stressed areas is zero, as it neither withdraws nor discharges water in these regions.
Conserving biodiversity is also central to human health and well-being. While Grifols' activities do not involve agriculture or forestry and as such, are not considered to have a significant impact on biodiversity or ecosystems, the company still remains committed to protecting and enhancing biodiversity on its own properties. Grifols does not work with genetically modified organisms (GMOs) or products that could generate persistent organic compounds or significant nitrogen or phosphorus discharges and no material risks or opportunities related to biodiversity have been identified that could affect the company's development.
| Actions | Metrics and Targets |
|---|---|
| • Programs for the protection and conservation of biodiversity in company owned natural areas and other areas of |
Under Grifols 2030 Agenda • Protect biodiversity in company-owned natural areas to capture CO2 |
| influence | Under the Environmental Program |
| • Participate in biodiversity preservation programs | |
Grifols' Biodiversity Policy outlines its commitments to biodiversity conservation with an approach aligned with key international frameworks, including the United Nations Convention on Biological Diversity (1992), the EU Biodiversity Strategy for 2030 (2020), the Kunming-Montreal Global Biodiversity Framework (2022) and the 2030 Agenda for Sustainable Development (2015).
The policy has been developed in line with Grifols' regulatory frameworks, which include the Sustainability Policy, Environmental Policy, Climate Action Policy, Energy Policy, Human Rights Policy and the Grifols 2030 Agenda.
Grifols is committed to protecting and restoring ecosystems, conducting risk assessments across its value chain to identify and mitigate biodiversity impacts and implementing measures to reduce natural resource use, particularly water. The company also collaborates with local communities to promote the conservation and protection of ecologically valuable areas.
Biodiversity forms one of the three key cornerstones of Grifols' 2023- 2026 Corporate Environmental Program, which sets specific targets and initiatives to achieve them. Grifols monitors and evaluates progress toward these targets as part of its broader environmental strategy.
| Biodiversity-related objectives | |||
|---|---|---|---|
| Establish biodiversity | Maintain Wildlife Habitat Council (WHC) certification to protect biodiversity in Grifols' natural areas. | ||
| protection programs in natural areas owned by Grifols and other areas of influence. |
Protect biodiversity in areas of influence through collaborations with external organizations: | ||
| • Rivus Foundation, dedicated to the restoration and conservation of river systems and their heritage. | |||
| • Associació Sèlvans, focused on protecting a centuries-old forest of recognized ecological value. |
General Environment Social Governance Annexes Biodiversity
Grifols does not operate in areas legally protected for biodiversity or in ecologically significant zones. However, it prioritizes locations with natural areas within its facilities or under its influence. As part of this commitment, Grifols actively protects biodiversity through two key initiatives–one in the U.S. and another in Spain.
Grifols' Wildlife programs in the U.S. focus primarily on launching conservation initiatives in the Clayton (North Carolina) protected natural area. In Spain, Grifols has an ongoing collaboration agreement to preserve and protect the watersheds of two rivers in Catalonia
As part of its environmental management system, Grifols assesses potential environmental risks at its U.S. facilities in Clayton, including those related to biodiversity impact.
Grifols owns over 121 hectares of forest adjacent to its production facilities in Clayton, North Carolina. This protected area is an ideal habitat for numerous aquatic and terrestrial species and is certified by the Wildlife at Work and Corporate Lands for Learning programs, both of which were launched by the Wildlife Habitat Council (WHC).
Conservation actions* in 2024:
*Key actions taken under each conservation program.
In 2024, Grifols continued its collaboration with the RIVUS Foundation, dedicated to research, education and volunteer initiatives to promote the conservation of the Besòs and Tordera river basins. Grifols supports the foundation's awareness programs in schools in reflection of its environmental commitment to its local surroundings.
This year, efforts have focused on environmental education, awareness and training for the educational community and the general public.
For more details on the initiative, see "Social Action-Patients" chapter.
In 2023, Grifols signed a sponsorship agreement with Associació Sèlvans to help preserve the natural forest heritage of singular ecological value.
Grifols' continued support in 2024 enabled the preservation of the "Grifols Centennial Forest," a sanctuary that promotes human health and wellbeing, serves as a refuge for remarkable biodiversity, and counteracts climate change.
Grifols has developed several awareness initiatives through this sponsorship, including training programs, a forest itinerary and adapting the space to provide forest therapy.
In addition to donating funds to the Ecken Wecken Foundation ("Awakening Corners"), employees from Grifols' German donation centers committed to sponsoring trees near the Leipzig headquarters.
We preserve 121+ hectares, equivalent to more than 150 football fields
The circular economy is at the heart of Grifols' operations, prioritizing the efficient use of resources and actively working to reduce waste. This goal of this strategy is to embrace the company's transition toward a low-carbon economy and minimize environmental impacts at every stage of the life cycle.
| E5 CIRCULAR ECONOMY |
||||
|---|---|---|---|---|
| Material IROs | Typology | Description | ||
| RESOURCE INFLOWS, INCLUDING USE | ||||
| Pressure on natural resources | - + OO SP |
Grifols is actively working to reduce its fossil fuel consumption, although it does not use coal directly. Its U.S. facilities account for 57% of the company's natural gas consumption. Additionally, Grifols continues to reduce pressure on other natural resources by integrating recycling, recovery and reuse measures that support the transition to a circular economy. |
||
| Dependence on plasma and other essential raw materials |
R | Plasma is a critical raw material in the production of plasma-derived medicines. Grifols has demonstrated resilience following the COVID-19 pandemic and has the expertise to manage potential risks related to plasma supply constraints caused by socioeconomic and geopolitical factors. The company also supports various public-private initiatives to enhance self-sufficiency1 |
||
| RESOURCE OUTFLOWS RELATED TO PRODUCTS AND SERVICES | ||||
| Waste recovery | + OO |
Promoting a circular economy through waste recovery initiatives in pharmaceutical operations helps conserve resources and strengthens a circular economy approach. |
||
| WASTE | ||||
| Waste generation | - + OO SP |
Grifols works towards responsible waste management, seeking to minimize its environmental impact while promoting recycling and reuse practices. |
||
| 1. More details: Section 3 of "Social impact on Donors-ESRS S3 |
| Material Sub-Topic | Policies | Actions | Metrics and Targets |
|---|---|---|---|
| Resource inflows, including use |
• Environmental Policy • Sustainability Policy |
• Drive circular economy principles at all stages of the product and service lifecycle* • Prioritize the efficient use of materials, water, and energy • Promote the use of low-impact materials in the design and development of production facilities and buildings |
Under Grifols 2030 Agenda • Continue implementing circular economy measures at every stage of the operational lifecycle Under the 2023-2026 Corporate Environmental Program: • Increase the use of recycled materials in Diagnostic |
| Resource outflows related to products and services |
• Promote the use of organic products (sorbitol and polyethylene glycol) • Continue maximizing the use of non-eligible plasma through the Bio Supplies unit • Explore further alternatives for non-eligible plasma |
Under the Environmental Program • Maintain "Zero Waste to Landfill" certification |
|
| Residuos | • Minimize and recover waste generated | Under the Environmental Program • Maintain "Zero Waste to Landfill" certification • Reduce waste generation by 1,800 tons annually |
|
| *See detailed actions by stage |
The circular economy is one of the three cornerstones of Grifols' 2023- 2026 Corporate Environmental Program, which outlines specific objectives to optimize resource use and minimize waste. These objectives focus on reducing consumption, maximizing raw material utilization and promoting reuse, recycling and resource regeneration whenever possible.
Grifols continuously evaluates and monitors progress toward the goals set out in its 2023-2026 Corporate Environmental Program and the Grifols 2030 Agenda.
| DEGREE OF COMPLIANCE WITH ACTIONS AT YEAR END 2024 | 56.07% | |
|---|---|---|
| Targets related to the circular economy | ||
| Maintain "Zero Waste to Landfill" certification |
Maintain "Zero Waste to Landfill" certification | |
| Reduce annual waste generation by 1,800 metric tons |
Reduce waste generation by installing an ethanol distillation tower Annual reduction of 1,785 metric tons, |
|
| Reduce plastic waste from packaging and raw material processing Annual reduction of 75 metric tons. |
||
| Reduce cardboard waste from plasma storage and reagent packaging Annual reduction of 5 metric tons Reduce packaging waste from cafeteria Annual reduction of 2 metric tons |
||
| Increase the use of recycled materials |
Implement use of recycled cardboard in packaging materials |
As part of its Sustainability Policy, Grifols is committed to its surroundings and sustainable development, promoting the rational use and optimization of natural resources as well as improving waste recycling and recovery.
To achieve this, the circular economy concept is at the foundation of Grifols' environmental management. The company's Environmental Policy specifically sets out the goal of fostering circular economy principles across all stages of the product and service lifecycle, prioritizing the efficient use of materials, water and energy, while minimizing and recovering waste.

More details: "Water Resources" section (ESRS-E3).

Plasma is the primary raw material used to produce plasma-derived medicines. It is managed through the Plasma Procurement business unit, which together with Biopharma, oversees the production of plasma-derived medicines and accounts for more than 84% of Grifols' revenue. Plasma is sourced from qualified donors.
Ethanol, polyethylene glycol and sorbitol are primarily used in the fractionation and purification of various plasma proteins. Through plasma fractionation, Grifols is able to extract proteins with therapeutic properties for commercial use. This process involves subjecting the plasma to successive temperature, pH and ethanol concentration adjustments, each of which facilitates the precipitation of a specific protein.
In the Diagnostic Business Unit, the main raw material is the plastic used in the production of its diagnostic cards (DG-GelR), in addition to the base plates to manufacture auto-analyzers.
One of Grifols' priorities is optimizing processes to minimize the use of plastic. The company has been working toward this goal since 2023, implementing several measures, including removing the polyethylene bag previously used in each box of plasma archive samples, which saves 20,600 bags per year– equivalent to 0.642 tons of plastic annually. It has also modified the packaging of ethanol-based production waste to eliminate the use of plastic containers, resulting in an annual reduction of 75 tons of plastic.
Likewise, more than 17 million gloves used in U.S. plasma donation centers are now biodegradable.
For a detailed breakdown of main raw material consumption, see the tables at the end of this chapter
Grifols' Diagnostic business unit, which operates at the Parets del Vallès plant in Barcelona, has redesigned the packaging for DG Gel cards to incorporate more sustainable materials. The new packaging is made from 100% recycled cardboard and features a safer, more eco-friendly varnish. Additionally, it will now display a symbol indicating its full recyclability, along with details of the recycled materials used.
In 2024, Grifols optimized the washing cycle for plastic crates at its Plasma Procurement facilities in Barcelona by introducing a biodegradable detergent. This innovation has significantly reduced the frequency of washing, simplifying the process and reducing working hours. More importantly, it has also led to a substantial reduction in water and energy consumption, reinforcing Grifols' commitment to sustainable operations.
| PLASMA PROCUREMENT and | DIAGNOSTIC | BIO-SUPPLIES |
|---|---|---|
| BIOPHARMA | 10% of revenue | 3% of revenue |
| 84% of revenue | ||
| Auto-analyzers and | Biological material | |
| Plasma-derived medicines | diagnostic reagents | for research and diagnostics |
| Main products | ||
| Immunoglobulins Alpha-1 antitrypsin Albumin Coagulation factors Fibrinogen |
Blood typing tests Blood and plasma virus screening tests Manual and automated analyzers |
A significant portion of plasma deemed unsuitable for plasma-derived medicines is repurposed for these applications |
| INTERMEDIATE PRODUCTS | ||
|---|---|---|
| Maximum reuse of plasma |
Most of the plasma deemed unsuitable for fractionation is marketed through Bio Supplies to produce diagnostic and analytical reagents for research purposes. By 2024 more than 160,000 liters of plasma had been sold, resulting in the annual reuse of 160 tons of raw materials and consequently, the same volume in waste reduction. |
|
| Once all plasma proteins for therapeutic purposes have been obtained, the remaining paste is disposed of as waste and managed according to its composition and country: anaerobic digestion for the production of biogas; composting; controlled landfill for non-hazardous waste; or autoclave treatment and subsequent landfill disposal. |
||
| Management of intermediate products in Biopharma |
A polyethylene glycol (PEG) and sorbitol solution is used to separate and obtain Flebogamma® DIF intravenous immunoglobulin. After use, this solution is concentrated at Grifols' Barcelona facilities and marketed to additive manufacturers for use in the cement industry. In 2024, approximately 21,246 tons of aqueous solution of polyethylene glycol and sorbitol were transformed into 14,724 tons of product that is sold as raw material for other uses. |
More information: "Value Chain" section.
Product quality and safety are a top priority at Grifols, including their presentation in the most environmentally-sustainably packaging. To this end, the company performed a study in the European market comparing glass packaging to plastic bags for 100 mL format albumin, taking into account all phases of the life cycle analysis (LCA).
The study was conducted in collaboration with Grup Carles and the UNESCO Chair of Life Cycle and Climate Change ESCI-UPF in line with the ISO 14044 standard and using Gabi LCA software. After normalizing the results, the nine most relevant impact categories were analyzed in depth, as well as the water scarcity indicator.
While widely considered more harmful to ecosystems, plastic bags were found to have a lower environmental impact than glass vials, scoring higher in all impact categories analyzed. The change in the product's packaging reduces its carbon footprint, leading to a 55% reduction in water consumption and a 23% improvement in climate change overall.
By way of example, supplying 10,000 units of albumin (20%) in 100 mL doses in plastic bags instead of glass vials avoids 655 kg of CO2 e emission and 355 m3 of water consumption. This is equivalent to driving 3,930 km in a mid-range car and taking 3,500 five-minute showers.

Grifols' waste management strategy prioritizes prevention and reduction, promoting waste recovery over landfill disposal or incineration. The company's internal procedures outline a structured waste management hierarchy: prevention, preparation for reuse, recycling, other types of recovery (including energy recovery) and disposal.
Grifols continues to explore waste treatment initiatives, including recycling initiatives, anaerobic digestion and material and energy recovery. In 2024, its industrial facilities and Plasma Procurement donation centers combined generated 22,442 tons of waste, reflecting a 6% increase due to higher production levels.
In the same year, 47% of Grifols' waste was not allocated for disposal, of which 87% was non-hazardous and 13% hazardous.
Additionally, U.S. donation centers collaborated with waste management providers to replace single-use cardboard boxes for biohazardous waste with reusable plastic containers, preventing 503 tons of cardboard waste being generated.
Biopharma's industrial facilities in North Carolina avoided 99% of waste from reaching landfill through recycling, composting, anaerobic digestion and other waste management techniques. Up to 5% of waste is processed through energy recovery incineration. As a result, these facilities have maintained the highest rating in the "Zero Waste to Landfill Gold Operations" certification for the sixth consecutive year.
In 2024, several reports were requested from CHWMEG, an independent entity that audits waste management providers in the U.S.
For more detailed data on waste disposal, recycling and reuse, see the tables at the end of this chapter
Most of Grifols' products are used in hospitals, which have their own recycling and disposal criteria established by local health authorities.
Grifols' products designed for domestic use are dispensed in pharmacies or by hospital suppliers, each of which has its own procedures regarding the safe collection and disposal of self-injectable devices. Grifols participates in various drug waste management programs.
*Including anaerobic digestion, other energy recovery methods, and by-products
In Spain, the SIGRE program manages the collection of household medicine packaging and waste to ensure it is safely treated to protect the environment. Starting in 2025, Spain will expand the collection of pharmaceutical and medical product packaging to include the entire healthcare sector, not just pharmacies. This initiative will ensure that all packaging introduced into the Spanish market by Grifols is properly managed and complies with current regulations.
10.3% Reuse 0.6%
Composting
In the U.S., Grifols is a member of the Pharmaceutical Product Stewardship Work Group (PPSWG), a U.S.-based membership association that coordinates pharmaceutical manufacturer efforts to respond to state and local household medicine and sharps takeback laws. The company is a participating company in MED-Project USA and MED-Project LLC ("MED-Project"), owned by PPSWG, which serve as the stewardship organization designated by PPSWG members to implement and operate mandated household unwanted medicine and sharps take-back programs. The MyOldMeds.com website is provided by PPSWG as an easy way for patients to find a site near them to dispose of unwanted, unused or expired medicines from households.
For medicines that end up not being marketed or returned, Grifols uses waste handlers who separate and classify medicine packaging (paper, cardboard, glass, plastics, etc.) to be recycled by specialized companies. The medicines themselves are disposed of through an authorized waste management company, using incineration methods and incineration with energy recovery.
Grifols' main products are plasma medicines for intravenous, intramuscular or subcutaneous administration in healthcare centers. The biological origin of plasma medicines limits their impact on the environment since waste is primarily generated from their containers and packaging, most of which can be recycled. The drug package leaflets indicate the correct waste management practices for country-specific legislation.
| MAIN MATERIALS CONSUMED - BIOPHARMA | ||||
|---|---|---|---|---|
| Absolute value (T) | 2024 | 2023 | 2022 | |
| Sorbitol | 1,797 | 1,400 | 1,164 | |
| Ethanol | 2,513 | 2,652 | 3,225 | |
| Polyethylene glycol | 1,671 | 2,318 | 1,720 | |
| Glass packaging | 3,869 | 3,441 | 2,881 | |
| Total | 9,850 | 9,811 | 8,990 |
| MAIN MATERIALS CONSUMED - BIOPHARMA - BIOTEST | |||
|---|---|---|---|
| Absolute value (T) | 2024 | 2023 | 2022 |
| Sorbitol | 0 | 0.00 | 0.00 |
| Ethanol | 2,300 | 2,506 | 1,462 |
| Polyethylene glycol | 0 | 0.00 | 0.00 |
| Glass packaging | 332 | 284 | 218 |
| Total | 2,632 | 2,790 | 1,680 |
| MAIN MATERIALS CONSUMED - DIAGNOSTIC | |||
|---|---|---|---|
| Absolute value (T) | 2024 | 2023 | 2022 |
| Circuit boards (units) | 23,196 | 20,890 | 27,463 |
| PP Plastic Cards | 414 | 363 | 300 |
| Glass packaging | 69 | 60 | 21 |
| Plastic reagent packaging* | 862 | 1,168 | 30 |
| Red cell reagents (liters)** | 0 | 0 | 266,803 |
| PVC pellets, flat tubes and sheets | 9 | 0 | 14 |
*Plastic containers from the San Diego plant have been added to the calculation
**The data taken into account in previous years corresponds to production and not to purchasing. Therefore, it is no longer considered for calculation in 2023.
| MAIN MATERIALS CONSUMED - OTHERS | ||||
|---|---|---|---|---|
| Absolute value (T) | 2024 | 2023 | 2022 | |
| PP | 885 | 1,067 | 979 | |
| Glucose | 94 | 112 | 185 | |
| Sodium chloride | 259 | 281 | 210 | |
| Glass packaging | 227 | 350 | 526 | |
| Total | 1,465 | 1,810 | 1,900 |
| T | Treatment | 2024 | 2023 | 2022 | |
|---|---|---|---|---|---|
| Waste diverted from disposal |
Energy recovered and by-products | 879 | 722 | 673 | |
| Hazardous waste | Reused | 19 | 2 | 70 | |
| Recycled | 296 | 1,317 | 1,100 | ||
| Energy recovered and by-products | 4,220 | 6,721 | 5,551 | ||
| Reused | 282 | 256 | 231 | ||
| Non-hazardous waste | Recycled | 13,573 | 12,614 | 12,930 | |
| Composted | 5,314 | 3,847 | 2,195 | ||
| Waste directed to disposal |
Incineration (with energy recovery) | 511 | 470 | 336 | |
| Incineration (withou energy recovery) | 37 | 50 | 609 | ||
| Hazardous waste | Landfill disposal | 0 | 0 | 0 | |
| Other disposal treaments | 5,102 | 6,586 | 7,053 | ||
| Incineration (with energy recovery) | 0 | 11 | 0 | ||
| Incineration (withou energy recovery) | 18 | 21 | 16 | ||
| Non-hazardous waste | Landfill disposal | 20,495 | 17,674 | 13,097 | |
| Other disposal treaments | 1,062 | 827 | 1,091 | ||
| Total | 51,808 | 51,118 | 44,952 |
| T | Treatment | 2024 | 2023 | 2022 | |
|---|---|---|---|---|---|
| Energy recovered and by-products | 0 | 0 | 84 | ||
| Hazardous waste | Reused | 0 | 0 | 0 | |
| Recycled | 8,972 | 0 | 0 | ||
| Waste diverted from disposal |
Energy recovered and by-products | 1,336 | 0 | 36 | |
| Reused | 0 | 0 | 0 | ||
| Non-hazardous waste | Recycled | 441 | 0 | 1 | |
| Composted | 73 | 0 | 0 | ||
| Waste directed to disposal |
Incineration (with energy recovery) | 11 | 399 | 17 | |
| Incineration (withou energy recovery) | 0 | 9,340 | 19 | ||
| Hazardous waste | Landfill disposal | 0 | 28 | 1 | |
| Other disposal treaments | 83 | 0 | 5,397 | ||
| Incineration (with energy recovery) | 0 | 1,269 | 657 | ||
| Incineration (withou energy recovery) | 0 | 443 | 99 | ||
| Non-hazardous waste | Landfill disposal | 67 | 0 | 46 | |
| Other disposal treaments | 0 | 0 | 251 | ||
| Total | 10,983 | 11,479 | 6,608 |
| GRIFOLS | |
|---|---|
| --------- | -- |

General Environment Social Governance Annexes Circular Economy
| GENERATED WASTE BY TYPE AND DISPOSAL METHOD RELATIVE VALUE | |||||
|---|---|---|---|---|---|
| T/million euros | Treatment | 2024 | 2023 | 2022 | |
| Energy recovered and by-products | 0.13 | 0.12 | 0.12 | ||
| Hazardous waste | Reused | 0.00 | 0.00 | 0.01 | |
| Recycled | 0.04 | 0.22 | 0.02 | ||
| Waste diverted | Energy recovered and by-products | 0.63 | 1.10 | 0.97 | |
| from disposal | Reused | 0.04 | 0.04 | 0.04 | |
| Non-hazardous waste | Recycled | 2.02 | 2.07 | 2.27 | |
| Composted | 0.79 | 0.63 | 0.39 | ||
| Incineration (with energy recovery) | 0.08 | 0.08 | 0.06 | ||
| Incineration (withou energy recovery) | 0.01 | 0.01 | 0.11 | ||
| Hazardous waste | Landfill disposal | 0.00 | 0.00 | 0.00 | |
| Waste directed | Other disposal treaments | 0.76 | 1.08 | 1.24 | |
| to disposal | Incineration (with energy recovery) | 0.00 | 0.00 | 0.00 | |
| Incineration (withou energy recovery) | 0.00 | 0.00 | 0.00 | ||
| Non-hazardous waste | Landfill disposal | 3.05 | 2.90 | 2.30 | |
| Other disposal treaments | 0.16 | 0.14 | 0.19 | ||
| Total | 7.71 | 8.39 | 7.88 | ||
| GENERATED WASTE BY TYPE AND DISPOSAL METHOD RELATIVE VALUE - BIOTEST | |||||
| T/million euros | Treatment | 2024 | 2023 | 2022 | |
| Energy recovered and by-products | 0.00 | 0.00 | 0.12 | ||
| Hazardous waste | Reused | 0.00 | 0.00 | 0.01 | |
| Recycled | 17.56 | 0.00 | 0.19 | ||
| Waste diverted | Energy recovered and by-products | 2.62 | 0.00 | 0.97 | |
| from disposal | Reused | 0.00 | 0.00 | 0.04 | |
| Non-hazardous waste | Recycled | 0.86 | 0.00 | 2.27 | |
| Composted | 0.14 | 0.00 | 0.39 | ||
| Incineration (with energy recovery) | 0.02 | 0.01 | 0.06 | ||
| Incineration (withou energy recovery) | 0.00 | 0.29 | 0.11 | ||
| Hazardous waste | Landfill disposal | 0.00 | 0.00 | 0.00 | |
| Other disposal treaments | 0.16 | 0.00 | 1.24 | ||
| Waste directed to disposal |
Incineration (with energy recovery) | 0.00 | 0.04 | 0.00 | |
| Incineration (withou energy recovery) | 0.00 | 0.01 | 0.00 | ||
| Non-hazardous waste | Landfill disposal | 0.13 | 0.00 | 2.30 | |
| Other disposal treaments | 0.00 | 0.00 | 0.19 | ||
| Total | 21.49 | 0.36 | 7.89 | ||
| WASTE GENERATED (ABSOLUTE VALUE) BY BUSINESS UNIT | |||||
| T Biopharma+Plasma procurement |
2024 47,762 |
2023 47,817 |
2022 42,077 |
||
| Diagnostic | 2,121 | 1,322 | 1,143 | ||
| Bio Supplies | 467 | 358 | 99 | ||
| Others | 1,045 | 1,400 | 1,305 | ||
| Commercial affiliates Total |
413 51,808 |
222 51,119 |
330 44,954 |
||
| WASTE GENERATED (ABSOLUTE VALUE) BY BUSINESS UNIT - BIOTEST | |||||
| T | 2024 | 2023 | 2022 | ||
| Plasma Procurement | 498 | 586 | 181 | ||
| Biopharma | 10,485 | 10,823 | 6,325 |
Total 10,983 11,409 6,506
| General | Environment | Social | Governance | Annexes | |
|---|---|---|---|---|---|
| Circular Economy | |||||
| WASTE GENERATED (ABSOLUTE VALUE) BY COUNTRY | |||
|---|---|---|---|
| 2024 | 2023 | 2022 | |
| 6,014 | 5,759 | 5,287 | |
| 42,825 | 42,757 | 37,784 | |
| 2,969 | 2,603 | 1,883 | |
| 51,808 | 51,119 | 44,954 | |
| WASTE GENERATED (ABSOLUTE VALUE) BY COUNTRY - BIOTEST | |||
|---|---|---|---|
| T | 2024 | 2023 | 2022 |
| Germany | 10,469 | 10,936 | 6,385 |
| RoW | 514 | 473 | 222 |
| Total | 10,983 | 11,409 | 6,607 |
| TOTAL WASTE GENERATED BY HAZARDOUS CLASSIFICATION | |
|---|---|
| T | 2024 |
| Hazardous | 6,844 |
| Non-hazardous | 44,964 |
| Total | 51,808 |
| TOTAL WASTE GENERATED BY HAZARDOUS CLASSIFICATION - BIOTEST | |
|---|---|
| T | 2024 |
| Hazardous | 9,065 |
| Non-hazardous | 1,918 |
| Total | 10,983 |
| TOTAL WASTE TREATED (ALL METHODS) | |||
|---|---|---|---|
| T | 2024 | 2023 | 2022 |
| Biopharma+Plasma procurement | 25,320 | 24,439 | 1,730 |
| Diagnostic | 1,360 | 699 | 62 |
| Bio Supplies | 350 | 156 | 413 |
| Others | 145 | 292 | 983 |
| Commercial affiliates | 49 | 52 | 4,247 |
| Total | 27,224 | 25,638 | 7,435 |
| TOTAL WASTE TREATED (ALL METHODS) - BIOTEST | |
|---|---|
| T | 2024 |
| Plasma Procurement | 142 |
| Biopharma | 19 |
| Total | 161 |
| NON-RECYCLED WASTE | |
|---|---|
| % | 2024 |
| Biopharma+Plasma procurement | 53.01 |
| Diagnostic | 64.13 |
| Bio Supplies | 74.99 |
| Others | 13.85 |
| Commercial affiliates | 11.92 |
| Total | 52.55 |
| NON-RECYCLED WASTE - BIOTEST | |
|---|---|
| % | 2024 |
| Plasma Procurement | 22.21 |
| Biopharma | 0.18 |
| Total | 1.45 |
| Impacts, risks and opportunities | 82 |
|---|---|
| Overview of our people | 85 |
| Quality employment | 86 |
| Collective bargaining coverage and social dialogue | 89 |
| Health, safety and wellbeing of our employees | 90 |
| Training and skill development | 92 |
| Diversity and inclusion: equal treatment and opportunities | 96 |
| Key performance indicators of our people | 102 |
| Workers in the value chain - ESRS S2 | 128 |
| Impacts, risks and opportunities | 128 |
| Due diligence in the value chain | 130 |
| Plasma donors and comunities - ESRS S3 | 131 |
| Impacts, risks and opportunities | 131 |
| Donors overview | 133 |
| Donor and donation safety | 134 |
| Donation centers and their communities | 137 |
| Social action and community support: amplifying Grifols positive impact |
141 |
| Patients and healthcare professionals - ESRS S4 | 146 |
| Impacts, risks and opportunities | 146 |
| Patients overview | 148 |
| Striving for excellence in our value chain | 150 |
| Building trust-based relationships through transparency | 155 |
| Access to treatments and diagnosis | 159 |
| Innovation at Grifols | 163 |
81 2024 Non-Financial Information Statement and Sustainability reporting
Impacts, risks and opportunities 163 Overview of innovation at Grifols 165 An ethical approach to science and innovation 166 Innovation in treatments 167 Innovation in diagnostics 171 Digital innovation 171 Manufacturing innovation 172 Research collaborations and support 173
141
General Environment Social Governance Annexes Our people
We view our talent pool as our most valuable asset. In reflection of this commitment, Grifols aims to create high-quality employment while prioritizing the health, wellbeing and safety of our employees. We work to continuously improve labor conditions and foster equal opportunities for all, with a keen focus on the advancement of pay parity.
| S1 OUR PEOPLE |
|||
|---|---|---|---|
| Material IROs | Type | Description | |
| WORKING CONDITIONS | |||
| Generation of high-quality employment |
+ - OO |
Grifols is aware of the negative impacts associated with its status as a large organization. Since its origins, the company has been firmly committed to generating high-quality employment, ensuring a healthy work-life balance, and promoting ongoing dialogue between employee and company representatives. |
|
| Employee turnover and termination | R OO |
Grifols takes steps to assure its employees are seen and supported, working to reinforce its corporate culture and minimize the risk of strikes and/or employee churn. |
|
| Occupational accidents and diseases |
- OO |
Grifols' mission is to enhance people's health. Its operations can never put the health of its employees at risk. For this reason, it has robust resources and systems to minimize the probability of negative impacts and to promote the wellbeing of its employees. |
|
| Challenges in recruitment and talent retention |
R OO |
The industry currently faces a shortage of skilled workers. As part of its long-term strategy, Grifols aspires to attract candidates who are capable of driving its growth and who identify with its corporate culture. |
|
| EQUAL TREATMENT AND OPPORTUNITIES FOR ALL | |||
| Discrimination and workplace harassment |
- OO |
Grifols does not tolerate discrimination or workplace harassment. The company has implemented important initiatives to minimize the likelihood of their occurrence. |
|
| Gender equality | - OO |
Grifols continues to make inroads to achieve gender equality and contribute to a more equitable society. |
|
| OTHER WORK RELATED RIGHTS | |||
| Helping eradicate forced labor | + OO |
Grifols complies with the ILO conventions, contributing to the eradication of forced and compulsory labor, modern slavery and other labor-related human rights issues. |
|
The following policies, actions, metrics and targets enable Grifols to efficiently and effectively manage the key material IROs related to its workforce in alignment with its current reality.
| Material Sub-topics | Policies | Actions | Metrics and Targets |
|---|---|---|---|
| Working conditions | • Remuneration Policy • Global Training Policy • Corporate Internship Policy • Occupational Health and Safety Policy • Mental Health Policy • "Flexibility for U" Policy |
• Grifols Employer Branding Initiative • Grifols Performance System (GPS) • Grifols Employee Survey • Mental Health Plan • Wellbeing Plan • Corporate Health and Safety Program • Occupational Health and Awareness Training Programs • Management System for Subsidiaries and Internal (ISO 45001) and External (ISO 45001) Audits |
• Maintain employee turnover rate below industry average • Achieve 70% overall employee engagement rate per department • Deliver 100 hours of training hours/year/ person • Impart annual training to 70-80% of the workforce • Certify >75% of industrial installations as healthy workplaces • Earn ISO 45001 certification in >75% of installations • Decrease LTIFR (lost time injury frequency rate) by 15% |
| Equal treatment and opportunities for all |
• Diversity and Inclusion Policy • Diversity policy in the Composition of the Board of Directors • Global Recruitment and Selection Policy • Harassment Prevention Policy |
• Strategic Diversity and Inclusion Plan • Equal Opportunities Plan • Grifols Affirmative Action Plan • Grifols Women in Leadership Award |
• Increase the percentage of women in leadership roles to 50% • Increase the percentage of employees with disabilities to 3-5% of the total workforce • Ensure women comprise 50% of interviews for managerial positions |
| Other work-related rights |
• Human Rights Policy • Grifols Ethics Line Policy |
More information: "Grifols Performance System" section.
Principle 3: We uphold the freedom of association and the right to collective bargaining.
Principle 4: We support the eradication of all forms of forced and compulsory labor.
Principle 5: We support the eradication of child labor.
Principle 6: We support the elimination of discrimination with regard to employment and occupation.

The Executive Committee routinely monitors the performance and evolution of Grifols' core strategic plans regarding labor conditions, equal treatment and opportunities for all, and other labor rights, including indicators and action plans related to mental health, the findings from the 2024 employee survey, and the risk and impact analysis carried out for its global workforce, among other issues.
The Sustainability Steering Committee, of which Grifols Human Resources Department is a member, promotes the achievement of the objectives established in the Sustainability Master Plan and the aforementioned programs.
The Chief Human Resources & Talent Officer (CHRO) serves on the Executive Committee and regularly updates the CEO on the performance of Grifols' employee pool. In addition, the CHRO's functions also include the approval process for the various policies, programs, and economic and human capital resources required to reach organizational objectives.
Lastly, the Corporate Risk Committee, which reports to the Board of Directors, oversees the development of the risk management model and supervision of the most relevant risks, including those related to Grifols' employee base.
Grifols maintains open and active communication with its talent pool to identify the most relevant employee impacts, risks and opportunities. These proactive efforts enable the company to continuously improve its people management, design and implement high-impact action plans, and define objectives to further reinforce its employee commitment.
Solid communication is also critical in preventing and managing incidents, and nurturing a culture of safety, respect and responsibility.
In this regard, Grifols strives to ensure its employees are seen and supported, with several communication channels available where they can express their concerns. The company also conducts global surveys and qualitative work groups to gather employee insights and opinions, and has specific procedures to address their feedback. These include:
The company promotes open communication with direct supervisors, compliance personnel, legal advisors and the internal audit team, while providing a secure and confidential channel–the Grifols Ethics Line. Through this platform, employees and external parties can voice concerns about potential breaches of Grifols Code of Conduct, guaranteeing confidentiality and that all issues are investigated. The platform is available 24/7 via phone and online. The Ethics Line operates in accordance with the Grifols Ethics Line Policy.
Concerns, inquiries and claims raised outside the Grifols Ethics Line, such as those sent to corporate human resource emails or voiced to HR business personnel, must be treated confidentially and forwarded immediately to the Global Ombudsperson. Exceptions include concerns reported to Grifols' Human Resources and Legal Department in North America, which are addressed through country-specific reporting channels. Local procedures and contact platforms are included in the Grifols Ethics Line Policy.
For Grifols, staying attuned to the concerns and opinions of its employees is essential to maintain its status as a great place to work. For this reason, in 2024, the company once again conducted a new global engagement survey, with a more than 85% response rate. Among its findings, it revealed a 4-point percentage increase in engagement and organizational support from human resources compared to 2020, reflecting stronger engagement and a positive work environment. Additionally, 65% of survey respondents reported having positive emotional health.
First measured at Grifols in 2024, the eNPS (Employee Net Promoter Score) indicator enables the company to assess employee satisfaction. This new indicator, aligned with Grifols' Mental Health Plan, is based on leadership, personal and organizational factors.
This type of survey is relevant because when people are engaged and motivated, they feel more connected to the company and are less likely to leave the organization.

In 2024, Grifols' workforce increased by 5%, reaching a total of 4,408 employees in Spain; 13,534 employees in the U.S. following a 3% drop. The
" Our operations create quality employment, driving social progress.
Employees at the close of 2024
23,822
Permanent contracts
98%
General Environment Social Governance Annexes
Between 30-50 years
52%
With a talent pool of over 23,000 employees, Grifols recognizes its fundamental role in shaping the quality of life of its team members and their families. For this reason, as an employer, the company has always strived to offer quality employment that advances social progress and improves employees' quality of life. This is among OECD's objectives for sustainable development.
Grifols' quality employment includes competitive salaries, incentives and benefits that complement social protection systems, as well as health and wellness programs tailored to employee needs. These elements, combined with efforts to promote ongoing dialogue and work-life balance, are key factors to improving employee's perception of their workplace, reducing employee churn and attracting new talent.
In 2024, the company hired 6,531 people and noted a progressive decline in the employee churn rate from 45.1% in 2021 to 30.6% in 2023.
At the end of 2024, 100% of Grifols' employees had received fair compensation in accordance with the calculation indices outlined in Directive (EU) 2022/2041 of the European Parliament and the Council for European countries, and in in the United States, in accordance with the Wages and Fair Labor Standards Act.
Grifols also works to ensure that all employees receive a living wage in line with the economic context of each country. To this end, the company conducts an annual review based on cost of living indices and market salaries, periodically updating salary ranges where necessary.
The company's remuneration policy promotes meritocracy and equal opportunities, compensating team members for their professional performance, contribution to its sustainable growth and achievement of strategic objectives.
Grifols guarantees non-discrimination on the basis of gender, age, race, religion, sexual orientation and other personal factors.
While Grifols' remuneration policy aims to compensate employees objectively and consistently with their level of responsibility and performance, each country offers competitive remuneration packages adapted to local market practices.
As stipulated in Grifols' Remuneration Policy, the company carries out an external analysis every year to assess its compensation practices and ensure their competitiveness and alignment with other companies in the sector.
"
One of the world's best companies in 2024 according to Times magazine.

The company began updating its Compensation Policy in 2024 to address additional factors such as project-based pay, special bonuses, retention bonuses and supplementary pay, as well as to revise and publish its Expatriation Policy.
This update will facilitate a global approach for all employees regardless of location while adapting to local needs; create a holistic framework grounded in consistency, fairness, clarity and compliance while providing flexibility for specific situations; and simplify workflows by significantly reducing the number of approvals required.
These policies are global in scope and include norms regarding eligibility, pay criteria, approvals, amounts and benefits in the case of the Expatriate Policy.
Additionally, Grifols is currently working on a job evaluation project to establish a methodical and rational hierarchy of jobs based on their relative value to the organization, i.e. evaluation of roles and not the people who occupy them.
As of 2023, Grifols offers two incentive plans: a short-term incentive plan (STIP) extensive to the entire workforce, and a long-term incentive plan (LTIP) with stock options for approximately 220 Grifols employees, including executive directors and senior-level leaders.
These plans are generally predicated on the fulfilment of predetermined and quantifiable financial and non-financial (ESG) objectives, and contingent on positive individual performance evaluations. Both plans were ratified at the Annual General Shareholders' Meeting.
10% ESG
metrics 90% financial metrics based on EBITDA
Employee compensation packages feature several social benefits, which in most countries, include healthcare access and income-support instruments in the case of illness, unemployment benefits, which accrue from the first day of employment; workplace accidents and acquired disability; parental leave; retirement, and death and disability coverage.
Social protection systems differ from country to country. In designing its supplementary benefits, Grifols takes into account each country's standard practices, particularities and social welfare needs.
At the close of 2024, 100% of Grifols' workforce was covered by corporate welfare benefits:
In Spain, the primary social-benefits structure is public: its Social Security system supports individuals in specific circumstances including unemployment, death, retirement and illness, among others. In addition,
Grifols complements and encourages participation in employee pension plans for team members in specific categories by doubling their contribution.
Additionally, the Partial Retirement Agreement signed with Spanish trade unions came into effect in December 2019. This accord regulates partial retirement for Grifols' employees until December 2025.
The U.S. model transfers the coverage of retirement plans to the private sector and personal initiative, as established by Employee Retirement Income Security Act (ERISA) standards.
In the United States, Grifols offers employees the option of contributing to a 401(k) Retirement Plan, allocating a maximum of 5% of their annual salary based on individual contributions. With regard to illness or death, Grifols offers private coverage for all of its collaborators, which employees themselves can expand.
Ireland also has a public benefits system which supports individuals in situations such as unemployment, death, retirement or illness, among others. At the same time, Grifols offers a corporate pension plan based on a defined contribution scheme, which allows employees to increase their retirement savings by contributing 5% of their salary, which the company matches with an additional 5%.
Germany has a public benefit system in the event of unemployment, retirement, illness or death, which the company increases with contributions between 3% and 8%, which employees can increase.
Grifols' contributions to pension plans are outlined in the tables at the end of the chapter taking into account country-specific legal regulations and the characteristics of each model.
In the wake of the pandemic, finding qualified personnel for complex tasks has become especially challenging for many companies in the sector. Grifols aspires to attract candidates who can exponentially drive the company's growth and enrich its corporate culture.
The Grifols Employer Branding Initiative has been a key lever in increasing candidates' awareness of the company and its reputation as an outstanding employer. Under this plan, Grifols makes coordinated efforts to attract, develop and retain talent, bolster brand recognition, and enhance employee engagement.
Grifols' progress in recent years have allowed the company to successfully fill 6,083 positions in 2024, representing 28.8% of its total talent pool.
In 2024, Grifols launched the "Space for U" initiative with the aim of defining the optimal office model to meet its evolving needs and work practices, and attract and retain global talent. The company envisions its offices as forums that foster collaboration, boost employee wellbeing and maximize efficiency and sustainability. As in previous years, the company also continued to reinforce its network of partnerships with U.S. educational institutions and employment centers, building on efforts that began in 2022.
In today's global environment, Grifols recognizes the value that employees place on trust and flexibility in managing their work time while striking a balance between their personal and professional life.
This equilibrium is a key factor in sustaining workplace productivity, as employees who achieve a healthy work-life balance experience less stress, greater job satisfaction and higher engagement. Grifols' "Flexibility for U" initiative, in alignment with its Flexibility Policy, also promotes trust and mutual responsibility between the company and employees.
The program entails several actions to address the diverse employee profiles of Grifols' workforce.
In 2024, 64% of eligible employees participated in the program, which include the following elements:
In the U.S., Grifols has a four-week paid parental leave program to allow full-time employees to care for their newborns or adopted children under the age of 18.

Grifols promotes social dialogue founded on freedom of association and the right to collective bargaining, taking into account the unique cultural, historical, economic and political frameworks in its countries of operation. In addition to its cultivating open lines of communication, the company adapts its social dialogue to each country's specific context. These efforts strengthen Grifols' corporate culture and ensures employee needs are met.
Effective communication with workers' legal representation is essential for addressing the transversal issues that require collective bargaining across the company's various workplaces. The Spanish labor-relations system defines two types of company representation: trade union representation and unitary or elective representation. The company holds regular and extraordinary staff-related meetings with these representatives, who form part of trade union sections, work councils and employee delegations.
In France, Germany and other countries, Grifols regularly meets with workers' legal representation. In Italy, it discusses decisions that could impact collective working conditions with trade union organizations.
Grifols fully supports the fundamental right of association and collective bargaining in alignment with the Universal Declaration of Human Rights.
In Spain, Germany, Italy, France, Argentina and Brazil, 100% of Grifols employees work under collective agreements. Together, they represent 27.9% of the total workforce.
Since no industry-specific agreements exist in the United States, collective bargaining is carried out at the company level.
In 2024, 6,648 employees (27.9% of its total workforce) were covered by collective bargaining agreements, including 4,671 Grifols employees (19.6% of its total workforce) and 1,977 Biotest employees (8.3% of its total workforce).
Grifols' workforce is covered by collective bargaining agreements specific to each country. The company promotes social dialogue through ongoing communication with employee representatives.
| Collective bargaining coverage inside EEA | Social dialogue coverage inside EEA | |
|---|---|---|
| U.S. | 0.0% | NAP |
| Germany (without Biotest) | 0.0% | 85.5% |
| Spain | 100.0% | 89.5% |
Grifols prioritizes the health, safety and wellbeing of its employees from a holistic perspective, taking into account both the physical and mental impacts of its operations, while working to forge an organization-wide environment grounded in trust and resilience.
The company updated its Occupational Health and Safety Policy in 2024, highlighting its efforts to safeguard the health of employees and stakeholders, including the management of operational risks for contractors. These initiatives are complemented by specific practices to report accidents and incidents, including risk communications in Spain and near-miss reporting in the United States.
Grifols is also making strides in reducing the impact of work-related accidents and occupational illnesses, both physical and mental. These efforts contribute to lowering absenteeism, increasing employee engagement and boosting workforce productivity.
At the corporate level, Grifols establishes global health and safety objectives every year. Additionally, subsidiaries set their own occupational health and safety goals as a core component of its management systems.
Grifols' management programs are routinely monitored through an internal auditing system. In the case of manufacturing processes, the company conducts both internal audits and certification audits based on the international health and safety management system, ISO 45001. Commercial subsidiaries carry out self-assessments via annual questionnaires.
Grifols has an occupational health and safety structure in all of its countries of operation, as well as a Corporate Occupational Health and Safety Department that provides support to the entire group.
In Spain, Chile and Germany, where labor committees are legally mandated, Grifols has designated risk-prevention occupational health and safety representatives to serve on these entities. In 2024, a large part of Grifols' Spanish workforce was represented by a joint committee of employees and occupational health and safety leaders.
In Chile and Germany, these committees represent 100% of the workforce. There is formal representation in Grifols' other subsidiaries; in these countries, the company regularly communicates and consults with employees and sets up committees where they can participate and submit proposals. Each subsidiary defines the frequency of these meetings and the follow-up of plans, actions and measures.
| Management system | Grifols' installations in Spain and Emeryville, California plant are ISO 45001-certified. A three-year plan is under way to earn ISO 45001 certification in all U.S. manufacturing plants by 2030. Grifols international subsidiaries have country specific systems in adherence to corporate policy and standards. In 2024, the company rolled out a new global safety standard titled "Project Safety" and an Occupational Health and Safety Policy. |
|---|---|
| Hazard identification and risk mitigation |
Integration in the design phase of manufacturing plans, change processes and procurement of new equipment. In 2024, Grifols implemented a new global standard and conducted risk assessments at work centers in line with its Corporate Occupational Health and Safety Manual. |
| Occupational health and safety awareness and training initiatives |
All employees take part in training and informational sessions on occupational health and safety issues throughout their tenure at Grifols, from onboarding programs to update sessions on their specific role. In 2024, the company established behavior-based safety objectives and implemented them out in Germany. |
| Boosting employee wellbeing and health |
Grifols heads several programs in its core countries of operation. Rolled out in 2022, the "Take Care of Your Heart" program is a three-year wellness plan extensive to all subsidiaries. The initiative integrated two additional risk factors in 2024: sleep hygiene and tobacco use. A new mental-health wellness plan is currently in development. |
| Management in contractor operations | Production centers follow country-specific management procedures. In Spain and Ireland, contractors are required to provide information on their occupational risk-prevention measures on an IT platform in order to access Grifols installations. The procedures for each company are audited within the HS Corporate Audits. |
In 2022, Grifols launched a comprehensive three-year wellness plan aimed at reducing work-related health issues, both physical and mental. The plan specifically centered on improving employees' cardiovascular health, given that in Spain, 39% of occupational deaths are linked to cardiovascular disease, with a similar trend observed in the U.S. and other European countries.
The initial focus of the "Take Care of Your Heart" program was on mental health and physical exercise. In 2023, it expanded to include nutrition and alcohol use, and in 2024, incorporated sleep hygiene and tobacco use. By the end of these three phases, the program now comprehensively addresses the six key cardiovascular risk factors.
The program's initiatives, which comprise sports days, monthly wellness tips, early detection tools and specialized training sessions, have been implemented in Grifols' main operating centers including Spain, Germany, Ireland and the United States, benefiting over 9,000 employees in the past three years.
In 2019, the World Health Organization (WHO) estimated that 15% of working-age adults suffers from a mental disorder. In this regard, it highlighted the relevance of the workplace on people's mental health.
Grifols recognizes its responsibility is supporting and promoting the emotional, psychological and social wellbeing of its employees in their specific roles and work environment. Mental health conditions such as depression, anxiety and stress can have a profound impact on motivation, productivity and performance, often resulting in extended sick leaves.
In consequence, Grifols works to promote its employees' mental wellbeing, helping them effectively navigate work-related demands while maintaining emotional and psychological balance.
Grifols has a Mental Health Policy in place since 2023 focused along three core dimensions: prevention, detection and performance. The company introduced a new indicator in its Engagement Pulse Survey in 2024 to better gauge the mental health of its workforce. In tandem, Grifols' new Strategic Wellness Plan also centers on enhancing the emotional health of Grifols talent.
65% of respondents reported having positive emotional health according to Grifols' new emotional health indicator.
At Grifols, 100% of employees are covered by its occupational health and safety management system, a global framework dedicated to continuous improvement.
Employees based in the United States, Spain, Ireland and Germany account for roughly 94% of Grifols' total workforce. Different indicators are followed in each of its subsidiaries, including accident rates.
The company investigates all workplace accidents with and without leaves, minor incidents and commuting accidents in countries where these are regulated.
In the past few years, the accident frequency rate has progressively decreased, achieving a reduction of 5.41 compared to the 2021 frequency rate. Additionally, the implemented management system contributes to the absence of occupational diseases in Grifols' manufacturing centers.
The identified risks depend on the activity performed, although there are significant differences between production centers and plasma donation centers due to the nature of their activities. Evaluating these risks and establishing corrective actions to minimize them is key to preventive management.
In terms of fatal accidents, no incidents have been reported over the last five years.
More information on accident rates, occupational health issues and absenteeism are available in the tables included at the end of this chapter.
Grifols understands the importance of continuous education and skills development to developing a high-caliber employee base and attracting and retaining talent.
The company's programs aspire to prepare employees for success in dynamic, ever-evolving environments, efforts that ultimately drive enhanced organizational productivity and efficiency. Grifols' learning initiatives also foster talent retention and reduce employee turnover by offering opportunities for growth and professional advancement. By investing in ongoing development, the company attracts next-generation talent, drives workplace innovation and helps bridge the skills gap by aligning labor-market supply with demand.
Through global surveys and taskforces according to its evolving needs, Grifols identifies its employees' most critical concerns and designs concrete action plans to promote their professional development and education, while reinforcing employee engagement and enriching its corporate culture.
Grifols conducted a global Employee Survey in 2020, using its results the foundation to address the detected areas for improvement and the realities of its business over the last years. The company implemented various professional development programs based on the analysis of its findings, including the Talent Program, and this year, the GROW Program and the Strategy Program.
These programs, in addition to providing a theoretical foundation, equip participants with actionable insights and competencies specific to their professional context. In this way, they advance the company's professionalization and capacity to adapt to changing environments, facilitating smooth generational handovers.
Based on the results of its 2024 Global Satisfaction Survey, the company is conducting a detailed analysis which offers both a global overview and an evaluation of key business areas by professional level, country, gender and age. This process will enable Grifols to tailor future action plans to the diverse groups identified within its employee pool.

Created to promote a positive work environment by distinguishing and rewarding the contributions, job performance and conduct of Grifols employees in line with company values. The program is based on three pillars: corporate values, work anniversaries and outstanding performance. Grifols has granted over 94,000 awards since its creation in July 2022. In 2024, more than 45,000 recognitions have been awarded through its platform.
The company has other reward programs including the Lean IG: Recognition Awards, which distinguish all improvement proposals in the areas of safety, quality, service, productivity and environmental impact. Participation among Biopharma employees has been particularly high since the program's 2021 launch, with 800-plus proposals, many of which have been implemented.
According to a Gallup study, effective recognition programs lead to a 14% increase in productivity and a 31% reduction in employee turnover.

A global 12-month program designed to build and develop the generational succession of Grifols leaders. Its second edition was held in 2024 with 100 high-potential employees (50% women) in manager or senior manager positions. This program supports talent retention by promoting internal mobility, engages leaders in mentoring and job-rotation sessions, and helps ensure robust leadership aligned with the group's corporate culture.
Global program launched in 2024 for high-potential, high-performance employees. If offers senior technicians, specialists and emerging leaders the chance to learn through a combination of strategic knowledge and practical insights, which are applicable to their professional roles. Its first edition welcomed 50 participants.

Global professional development program launched in 2024 for top-tier executives, including Senior Directors and Vice Presidents. Spanning nine months, it represents a strategic investment in leadership growth, helping Grifols' most seasoned directors align their competencies with its evolving needs. With 30 participants in its inaugural edition, the initiative is delivered in collaboration with ESADE Business School, one of the world's most prestigious learning institutions.
The Grifols Performance System (GPS) is an organization-wide process carried out every year to ensure managers properly evaluate their team members' professional performance and provide adequate feedback.
The GPS is primarily used to assess employees' competencies as outlined in the Grifols MAP model (competency model in line with Grifols values) and their potential based on Grifols potential model (aspiration + commitment + agility).
A calibration phase is performed before the assessment to ensure managers utilize the same criteria when measuring their employees' potential and performance. This process is carried out in collaboration with the leadership teams of each business area to guarantee fairness and minimize bias (Talent Review based on the Nine Box matrix).
All GPS processes are guided by a shared document between the manager and the employee, which includes current objectives, performance appraisals, professional development actions, overall performance scores and a talent review (performance + potential).
Grifols is committed to evaluating 100% of its employee base through the GPS. In 2024, 99.77% of employees participated in the evaluation system, including with 99.65% of women and 99.91% of men taking part. GPS results are also analyzed from a gender perspective.
GPS IS A COMPREHENSIVE YEARLY ASSESSMENT
The company partners with various educational institutions, primarily universities, to establish formal agreements for corporate internships. Grifols internships allow students to supplement their classroom knowledge by acquiring new skills and actionable insights for the future careers.
As outlined in Grifols' Internship Policy, created in 2017, students are assigned a company tutor or representative who supports them throughout their internship. Corporate internships last between six and 18 months.


GPS assessments also help guide decisions on promotions, internal job changes, the design of individual development plans and participation in talent programs, among other areas.
The GPS, combined with the calibration (Talent Review) conducted midway through the process, plays a crucial role in shaping the company's future. By transforming data into actionable insights, it has a long-term impact by informing strategic decisions made about Grifols' talent pipeline.
Employee training is a cornerstone of professional and talent development. Grifols ensures all employees have access to continuous training and learning opportunities as part of its global training and development strategy. This approach, in line with Grifols core strategic objectives and corporate values, allows the company to detect and address individual, team, business and organizational needs.
All training initiatives are carefully evaluated to measure both participant satisfaction and the practical application of learned concepts in the workplace, promoting a culture of continuous learning and personal accountability. These initiatives continuously evolve in response to changing business priorities, global dynamics and emerging trends.
In 2024, Grifols took an important step forward with the unveiling of the "Copilot" tool, a generative AI solution available to all employees. The company hosted interactive webinars on its features to help employees unlock its full potential. Grifols also offers flexible, on-demand learning options, empowering employees to personalize their learning and access resources that best align with their explicit development goals.

5,867,705 68.2% women 31.4% men 0.4% undeclared and others
different cultures and business protocols
Training on occup. health, safety and environmental issues
46,542 hours and 2% of Grifols' workforce

training in Biotest
52,370 50% women
50% men
More information on training hours is available in the tables at the end of this chapter.
94 2024 Non-Financial Information Statement and Sustainability reporting
Programs designed to strengthen core leadership competencies, including communication, emotional intelligence and conflict resolution.
Executive development benefits global organizations by improving strategic decision-making and boosting productivity through more efficient team management. At the same time, it increases talent retention by fostering positive work environments, facilitates adaptation to change during periods of transformation, and drives continuous innovation through mentorship and support initiatives.

20 programs/training sessions in 2024 336 employees participated in 2024 ~2,700 executives formed over the last 5 years EUR 822,000+ allocated to educational initiatives
As part of its commitment to the continuous development of its employees and diverse social stakeholders, in 2009 the company established the Grifols Academy, which includes the Professional Development Academy and the Plasmapheresis Academy. It offers educational and professional development opportunities to its global workforce and reinforces corporate values, while enabling the exchange of plasma-sector knowledge.

High-quality programs and workshops featuring industry experts and other resources to help Grifols employees excel in changing business environments. In 2024, the Academy revised its value proposition and program portfolio, and launched two new initiatives: an online learning platform and a Speaker Series in Spain and global subsidiaries.
| 2024 | 2023 | 2022 | |
|---|---|---|---|
| No. of participants | 2,686 | 2,399 | 2,001 |
| No. of learning sessions | 192 | 108 | 135 |
| Online training hours | 7,033 | 3,206 | 4,468 |
General and specialized programs on plasma science to accelerate the professional and educational development opportunities of Grifols' U.S. based employees, helping reinforce its unique value proposition.
The Plasmapheresis Academy was granted a five-year recognition by The Accrediting Commission of the Accrediting Council for Continued Education & Training (ACCET), valid until December 2024. It earned its first accreditation in 2015.
| 2024 | 2023 | 2022 | |
|---|---|---|---|
| No. of participants | 9,741 | 6,573 | 13,736 |
| On-site participants | 302 | 491 | 893 |
| Online participants | 0 | 0 | 110 |
| No. of online training hours | 11,695 | 9,790 | 39,099 |
| No. of distance-learning hours | 0 | 0 | 2,468 |
Grifols gives employees the option of learning outside the organization to gain new competencies and knowledge, which increases productivity. The program encourages workplace motivation and engagement by making employees feel valued.
The reimbursement program also drives innovation by exposing employees to new ideas and insights, in turn reinforcing Grifols' competitive positioning. Depending on program modality, the grant covers between 33% (€5,000 maximum per year) and 50% (€736 maximum per person and course).

281 beneficiaries of educational grants EUR 659,772 allocated to educational grants 38% of subsidies for STEM training
Age Gender identity or expression Gender National origin Sexual orientation Mental/physical ability
Year 1
• Activities/program for women in leadership • Top-tier management sponsors • Awareness campaigns • Review of HR programs/processes • D&I ambassador program in Spain the U.S.
Language and communication skills Income Religion Appearance Work experience
| 2020 (prior to the | ||
|---|---|---|
| program launch) | 2024 | |
| People with disabilities | 2.5% | 3.8% |
| Nationalities | 88 | 97 |
| Female representation in leadership positions | 37.2% | 40.6% |
GOALS Provide an inclusive and safe workplace for all employees Elevate D&I competencies through education Represent the communities served throughout the employee base Achieve the objectives outlined in Grifols 2030 Agenda CATEGORIES
Race/ethnicity Educational level Political ideology Family Organizational role
ANNUAL ACTION PLANS
| EVOLUTION OF THE DIVERSITY PLAN 2021-2024 | ||
|---|---|---|
| 2020 (prior to the program launch) |
2024 | |
| People with disabilities | 2.5% | 3.8% |
| Nationalities | 88 | 97 |
For Grifols, diversity is key to generating new ideas and driving innovation. Different perspectives, experiences and mindsets enrich the exchange of ideas, and allow organizations to find creative solutions by approaching problems from various angles. By valuing diversity, the company is also better equipped to meet the diverse needs of its global markets and customers, while cultivating an inclusive environment that bolsters employee engagement and participation.
Grifols completed its first Diversity and Inclusion (D&I) Plan in 2024. In force since 2021, the plan aspires to advance gender equity and increase the inclusion of people with disabilities, minority representation, and intergenerational and cross-cultural collaboration in the workplace.
In parallel, the company designed and developed awareness and training initiatives to foster a more inclusive and diverse workplace. These efforts included dynamic sessions, educational resources and collaborations with local organizations that support minority groups.
Grifols also promotes inclusivity through its D&I Ambassador team in the United States, which expanded in 2024 with the creation of a new group in Spain. D&I Ambassadors receive specialized training, act as key advocates on inclusion-related issues and promote the diversity agenda within their teams and day-to-day operations, playing a vital role in building a more inclusive and positive work environment.
Grifols rolled out its second three-year Diversity and Inclusion Plan in 2024
opportunities from the moment of hire, through the employee's development culture founded on psychological safety and freedom where everyone can be their authentic selves.
The key priorities of the new plan are to:
The implementation of the new plan is supported globally, while being tailored to the cultural context of each country by local D&I teams.
As part of its commitment, Grifols is dedicated to promoting equal and until the end of their tenure. To this end, it works to forge a corporate
to boost the recruitment, development and retention of high-performing employees.

More details and tables on the composition of Grifols' workforce by fiscal year are available at the end of this chapter.

| Share in total workforce |
Share in management positions |
|
|---|---|---|
| l Caucasian | 40.7% | 61.6% |
| l Hispanic | 25.3% | 11.9% |
| l African American | 21.1% | 5.5% |
| l Asian | 6.0% | 13.9% |
| l Hawaiian /Other Pacific Islander | 0.4% | 0.1% |
| l Native American /Native Alaskan | 0.7% | 0.5% |
| l Two or more races | 4.3% | 2.2% |
| l Unspecified | 1.5% | 4.3% |
More details and tables on the composition of Grifols' workforce by fiscal year are available at the end of this chapter.
Grifols upholds a zero-tolerance policy against all forms of harassment and discrimination, reinforcing its staunch commitment to ensuring an inclusive, respectful and safe workplace for all employees.
Discrimination or harassment of any kind–whether based on gender, race, sexual orientation, religion, disability or other factors–is strictly prohibited. Grifols has robust preventive measures in place and responds immediately in the event of possible inappropriate conduct to safeguard the dignity and human rights of every individual.
Grifols' affirmative action plans included 65 measures in 2024, 67 measures in 2023 and 110 measures in 2022.
Grifols' development initiatives include prevention training activities, including courses delivered under the Equal Opportunity Plan and Grifols Ethics Line, among others. Both courses are mandatory for Grifols employees.
In 2024, the company received 31 incidents of discrimination reports out of 21,156 employees, compared to 55 incident reports in 2023 out of 21,144 employees, and 36 incidents in 2022 out of 23,947 employees. In Biotest, 2 reports of incidents related to discrimination were filed in 2024 out of 2,666 employees. In 2023 and 2022 Biotest filed 0 incidents.
During the reporting period, the number of labor incidents, claims, serious human rights violations involving its own personnel, as well as significant labor-related fines, sanctions or compensations was 0.

The company methodically investigated and assessed all complaints. While none were deemed discriminatory in legal terms, the company took proactive steps to guarantee a discrimination-free workplace, including by training and awareness sessions and disciplinary measures when appropriate.
As mentioned at the beginning of this chapter, the company has a procedure to protect employees who report instances of discrimination under the umbrella of Grifols Ethics Line.
Harassment is a form of discrimination. Established in 2021, Grifols Harassment Prevention Policy strives to eradicate any type of offensive verbal, physical or visual actions or behaviors directed at employees on the basis of gender, color, race, ethnicity, religion, national origin, age, disability, pregnancy, sexual orientation or gender identity or expression that could create an intimidating, offensive or hostile work environment or undermine employees' professional performance.
The policy, translated into 11 languages and adapted to local regulations, reflects Grifols' solid commitment to three core pillars:
The Harassment Prevention Policy lists specific behaviors prohibited by the organization, along with escalation processes and disciplinary measures in the event of violations.
Grifols provides employee training to reinforce the policy's provisions, recognizing both as essential for preventing, addressing and correcting any infringements.
5,100+ people trained in Grifols Harassment Prevention Policy
In 2024, 3.8% of Grifols' workforce included people with disabilities, with 894 in total.
| Grifols | Biotest | |
|---|---|---|
| 2022 | 899 | 59 |
| 2023 | 785 | 67 |
| 2024 | 818 | 76 |
Grifols is committed to employing people with disabilities, and only adopts alternative measures as defined by the General Disability Law applicable to private- and public-sector organizations in Spain.
In the U.S., Grifols complies with the employment provisions of the Americans with Disabilities Act (ADA), a federal law designed to prevent discrimination and provide equal opportunities for people with disabilities.
As part of its Strategic Plan for Diversity, the company has also created taskforces in the U.S. Germany, Ireland and Spain to boost the recruitment of diverse talent and enhance the experience of employees with disabilities.
Action lines in 2024 included:
Grifols also promotes universal accessibility for people with disabilities. When a person with a disability is hired, the company takes all the necessary steps to adequately adapt their work station and environment. The company complies will all legal regulations in its new buildings and installations, and adapts existing structures whenever necessary, applying the principles of accessibility, including the elimination of architectural barriers.
Grifols Strategic Plan for Diversity includes the integration of people with disabilities.
Grifols worked along several fronts to advance the equality and equity goals outlined in its 2030 Agenda, with gender equality as a common thread. Among other actions, the company reviewed promotion processes to identify opportunities for improvement, ensured the use of inclusive language in its communications, made efforts to boost the visibility of women in STEM roles, and focused corporate volunteering on supporting the employability of women at risk of exclusion.
Aligned with our commitment to diversity and inclusion, Grifols has expanded its STEM WOMEN PROGRAM internship initiative. Grifols is now in the second edition of the program and have brought on seven new engineers in key areas like software and engineering. The engineers from the first edition have taken on mentoring roles for their new colleagues.
The company also boosted its presence at events like the STEM Careers Congress in Ireland, one of the leading events for female tech talent, drawing over 4,000 attendees. Our goal is to promote gender diversity in the STEM sector and provide professional development opportunities for talented women.
In all our audiovisual productions, we've ensured gender equity representation to keep our external image aligned with the reality of Grifols.
In Spain, Grifols has a gender equality plan negotiated with the legal representatives of the employees. This plan applies to all employees in Spain in line with local regulations.
The plan's 41 gender-equality measures include efforts to guarantee equal pay and opportunities in recruitment processes and internal promotions, and ensure harassment-free workplaces. In force until 2026 and publicly available on REGCON, it led to women representing 60,3% of promotions in 2024.
Its measures are reviewed in committee meetings focused on the implementation, monitoring and evaluation of Grifols' gender equality plan.
Among the plan's core components, Grifols updated its protocol for addressing and managing cases of workplace harassment, sexual harassment, harassment based on sex, gender or sexual orientation, and other forms of violence in the workplace.
The company also enhanced internal communication to spread awareness and understanding of the protocol. Other initiatives included a review of onboarding program materials to promote this important resource, updated training for employees involved in protocol procedures, and the development an informational guide on gender-based violence.
To ensure compliance with current equality regulations within Grifols, the company has requested that partner companies providing services at its facilities submit their harassment protocols. Additionally, the inclusion of equality clauses is required in third-party contracts.
In other regions, Grifols applies the principles of equal opportunities defined in the Global Diversity and Inclusion Policy.
Grifols launched the Women in Leadership Awards in 2023 memory of Dr. Marilyn Rosa-Bray, an inspirational Grifols leader for 24 years and an outstanding contributor to the plasma industry. The Women in Leadership Awards recognize the work and contributions of women at Grifols, particularly in the field of science. The final decision is made by a jury of members of Grifols Sustainability Committee.
Grifols joined the Empowering Women's Talent and Diversity Leading Company programs in 2024. Through its participation, the company gains exclusive access to high-impact activities and training sessions for its D&I ambassador team, committed to promoting diversity and inclusion within the organization.
57.4% of employees are women
40.61% of Senior Management, Directors and Executives positions are filled by women
60.3% of promotions correspond to women
65% of new hires are women
41% of directors (179) 43% of senior management (251) 47% of management (608) 49% of senior professionals (1,020) 53% of professionals (1,463) 62% of administrative and manufacturing staff (8,591) *Excluding Biotest
Grifols is firmly committed to effective equality, ensuring equal opportunities and pay regardless of gender. Through its annual analysis of adjusted and unadjusted pay gaps, the company aims to continue promoting gender equality by identifying salary differences between men and women. In 2024, Grifols received external support from the global consulting firm EY to ensure the utmost rigor and transparency in its analysis.
In accordance with Delegated Regulation (EU) 2023/27721 , the gender pay gap is defined as "the difference between the average remuneration levels of female and male employees, expressed as a percentage of the average remuneration level of male employees".
Average remuneration was calculated using the employee's base salary, other fixed supplements and additional compensation–whether in cash or in kind–earned directly or indirectly ("supplementary or variable components").
Compensation was then divided by the number of hours worked during the year to measure pay per unit of time. In consequence, 2024 data is not comparable to previous years, which considered 100% of employees' fixed salary.
Compensation information was also segmented by country (Spain, United States, Ireland and Germany) and by professional category (Executives, Directors, Senior Management, Management, Senior Professional, Professional, Administrative Staff/Manufacturing Operators). The analysis also includes insights on the potential impact of objective factors like job type and country of employment on the gender pay gap ("adjusted pay gap").
The adjusted pay gap considered more accurate than the unadjusted pay gap since it applies econometric models that enable comparing men's and women's salaries at 100% employment, and isolating the effects generated by socioeconomic differences (age, seniority, geographic area or educational level) or job characteristics (type of working day, type of activity or professional category).
For the purposes of this report, the pay gap was analyzed in Spain, the U.S., Germany and Ireland, which collectively represent more than 90% of the group's employee base.
At Grifols, pay gaps by country are below national averages according to the World Economic Forum's Global Gender Gap Report 2024.
The company's results by professional category highlight its progress in increasing the representation of women in top-tier leadership, a key lever in advancing pay equality. Testament to these efforts, the percentage of women in Grifols senior positions has expanded notably in recent years, in 2024 accounting for 24.51% and 41.18% of Executive and Directors positions, respectively.
Gender equality is also emphasized in Grifols 2030 Agenda, with a target of achieving 50% women in Senior Management roles. At the close of 2024, this percentage stood at 43.61%.
In Grifols' view, strengthening the representation of women in these professional categories will help narrow the gender pay gap.
At the same time, the company also works to advance pay parity by promoting women in STEM (Science, Technology, Engineering and Mathematics). The company works to counter the historical gender imbalance in STEM, where cultural factors have led to a predominance of men in technical careers. In this regard, it has several initiatives in place to identify STEM positions and adopt measures to encourage greater female participation.
In addition to implementing a targeted action plan to address the two aforementioned factors due to their direct impact on the gender pay gap, Grifols is also working to improve its recruitment, salary review and promotion processes–key components of its 2024-2026 Diversity plan.
Specifically, the company strives to ensure that these processes are driven by individual performance evaluations by applying consistent, transparent criteria free from gender bias. At the same time, it promotes flexible work arrangements, ensuring equal access for all employees regardless of gender, and imparts specific training and professional development initiatives to strengthen its pipeline of female talent and facilitate the incorporation of women in leadership roles.
The company aims for women to represent 50% of candidates interviewed for managerial positions and above as defined in Grifols 2030 Agenda. The gap between the organization's highest-paid individual and the average employee salary is stood at 68.93 times at the close of 2024.
| Spain | U.S. | Ireland | Germany | |
|---|---|---|---|---|
| Pay gap by | ||||
| country2 | 31.20% | 28.80% | 28.90% | 36.40% |
| Adjusted pay | ||||
| gap3 | 4.72% | 1.31% | 4.25% | 2.52% |
| Unadjusted pay | ||||
| gap4 | 18.26% | 26.56% | 11.40% | 17.27% |
Source: Global Gender Gap Report 2024.
The adjusted pay gap is estimated using a multiple linear regression model that quantifies the relationship between predictor variables (objective factors) and the dependent variable (salary). By including gender as one of the predictor variables in the model, the effect of gender on salary can be isolated, controlling for other factors such as experience, education and working conditions. In this way, the difference in the coefficients for the gender variable represents the wage difference attributable solely to gender, after accounting for other relevant factors.
In accordance with the Delegated Regulation (EU) 2023/2772, the average wage includes the base salary, other fixed supplements, and any other remuneration, in cash or in kind, received directly or indirectly by the worker ("complementary or variable components").
An overview of remuneration tables is available at the end of this chapter.
1, Delegated Regulation (EU) 2023/2772 of the Commission, of July 31, 2023, supplementing Directive 2013/34/EU of the European Parliament and of the Council with regard to the rules for presenting sustainability information, published on December 22, 2023 (hereinafter, the "Delegated Regulation").

The following are the results of the wage gap analysis, broken down by country, to provide a more detailed view of the observed differences.
The unadjusted global pay gap stands at 18.26% compared to the national average of 31.20%. This significant difference is testament to Grifols' efforts to achieve pay equality.
The adjusted pay gap in Spain represents 13.54% of the total unadjusted pay difference, indicating that, after considering objective factors like position or experience, a pay difference of 4.72% remains.
When segmented by professional categories, some salary pay gaps are lower than this average percentage. These include Administrative Staff/ Manufacturing Operators, Senior Professional, Senior Management and Directors, the latter reflecting the category with the smallest adjusted gap, at 0.32%.
In the case of the Professional category, the pay gap was primarily attributed to allowances and performance-based bonuses, which are dependent on the specific conditions of the role and individual job performance.

20.8% people in Spain over the total workforce
In 2024, the unadjusted pay gap stands at 26.56%, below the national average of 28.80%. The company continues to make significant progress toward pay parity, while also actively promoting women's advancement into leadership roles.
The adjusted pay gap in 2024 is 1.31%, representing 25.25% of the total gross pay gap. This demonstrates a clear correlation between hourly wages and the objective criteria that determine compensation.
Moreover, over 75% of employees fall within the Administrative Staff/ Manufacturing Operators category, where the adjusted pay gap is -0.69%. This indicates that, on average, women in this category earn slightly more than their male counterparts.
64.0% people in the U.S. over the total workforce
60.93% are women 1.31% adjusted pay gap
The unadjusted pay gap in the country stands at 28.90% in 2024. Grifols in Ireland, with an 11.40% unadjusted gap and a 4.25% adjusted gap, is significantly below the national average.
Based on the analysis, the pay difference in the Senior Management is especially noteworthy: although men make up a larger share (64%), women, on average, earn 16.18% more than their male counterparts.
In the Professional category, the pay gap is primarily driven by allowances and performance-based bonuses, which are linked to the specific conditions of the role and individual performance.
2.1% people in Ireland over the total workforce
44.36% are women 4.25% adjusted pay gap
The unadjusted pay gap is 17.27%, well below the national average of 36.40%. When accounting for objective factors, the pay gap explains 14.75% of the difference, leaving an adjusted pay gap of only 2.52%.
By professional category, the adjusted pay gap for Administrative Staff/ Manufacturing Operators is near zero (0.35%). These categories represent 62% of Grifols' workforce in Germany.
In the Professional category, the pay gap is primarily driven by allowances and performance-based bonuses, which are linked to the specific conditions of the role and individual performance.
7.4% of people in Germany over the total workforce
Details on the gender pay gap are available in the tables at the end of this chapter.
| AVERAGE WORKFORCE BY COUNTRY | |||
|---|---|---|---|
| 2024 | 2023 | 2022 | |
| U.S. | 12,563 | 13,143 | 15,669 |
| Spain | 4,227 | 4,095 | 4,082 |
| Germany | 1,367 | 2,699 | |
| RoW | 1,526 | 2,781 | |
| Total | 19,676 | 20,019 | 22,450 |
| AVERAGE WORKFORCE BY COUNTRY - BIOTEST | ||
|---|---|---|
| 2024 | 2023 | |
| Germany | 1,967 | 1,950 |
| RoW | 501 | 537 |
| Total | 2,468 | 2,487 |
| 2024 | 2023 | 2022 | |||||||
|---|---|---|---|---|---|---|---|---|---|
| Permanent | Temporary | Total | Permanent | Temporary | Total | Permanent | Temporary | Total | |
| U.S. | 12,559 | 3 | 12,562 | 13,139 | 4 | 13,143 | 15,665 | 4 | 15,669 |
| Europe | 6,287 | 264 | 6,551 | 6,091 | 238 | 6,330 | 5,982 | 254 | 6,236 |
| RoW | 556 | 7 | 563 | 538 | 8 | 546 | 535 | 10 | 545 |
| Total | 19,402 | 274 | 19,676 | 19,768 | 250 | 20,019 | 22,181 | 268 | 22,450 |
| 2024 | 2023 | |||||||
|---|---|---|---|---|---|---|---|---|
| Permanent | Temporary | Total | Permanent | Temporary | Total | |||
| Europe | 2,363 | 104 | 2,468 | 2,335 | 153 | 2,487 | ||
| RoW | 0 | 0 | 0 | 0 | 0 | 0 | ||
| Total | 2,363 | 104 | 2,468 | 2,335 | 153 | 2,487 |
| AVERAGE WORKFORCE BY AGE | AVERAGE WORKFORCE BY AGE - BIOTEST | |||||
|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | 2024 | 2023 | ||
| <30 | 4,914 | 5,154 | 6,216 | <30 | 464 | 476 |
| 30-50 | 10,369 | 10,537 | 11,706 | 30-50 | 1379 | 1,333 |
| >50 | 4,393 | 4,327 | 4,528 | >50 | 625 | 679 |
| Total | 19,676 | 20,019 | 22,450 | Total | 2,468 | 2,487 |
| 2024 | 2023 | 2022 | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Permanent | Temporary | Total | Permanent | Temporary | Total | Permanent | Temporary | Total | ||
| Women | 10,942 | 157 | 11,099 | 11,318 | 140 | 11,459 | 13,217 | 145 | 13,362 | |
| Men | 8,346 | 117 | 8,463 | 8,403 | 110 | 8,513 | 8,938 | 124 | 9,062 | |
| Undeclared | 107 | 0 | 107 | |||||||
| Other | 7 | 0 | 7 | 47 | 0 | 47 | 26 | 0 | 26 | |
| Total | 19,402 | 274 | 19,676 | 19,768 | 250 | 20,019 | 22,181 | 268 | 22,450 |
| 2024 | 2023 | ||||||
|---|---|---|---|---|---|---|---|
| Permanent | Temporary | Total | Permanent | Temporary | Total | ||
| Women | 1,189 | 77 | 1,266 | 1,202 | 120 | 1,322 | |
| Men | 1,174 | 28 | 1,202 | 1,133 | 33 | 1,166 | |
| Total | 2,363 | 104 | 2,468 | 2,335 | 153 | 2,487 |
In compliance with the Corporate Sustainability Reporting Directive (CSRD), companies with 50 or more employees that represent at least 10% of their total workforce must disclose country-based social standards. In line with these mandates, Grifols' 2024 report separates data for Germany from the Rest of the World (ROW). In previous years, these two categories were reported as a consolidated figure.
Grifols and Biotest do not have employees on zero-hour contracts.
Grifols' salaried employee data by gender for the 2024 fiscal year is categorized into four groups: Women, Men, Undeclared and Other (gender as specified by the employees themselves, e.g., non-binary individuals). In the 2023 and 2022 fiscal years, the "Undeclared" and "Other" categories were consolidated into a single category as "Non-binary and Undeclared."
Biotest does not have employees in the "Undeclared" and "Other" categories. For this reason, its gender-related tables only report on Women and Men.
Grifols' average workforce was calculated as the average full-time equivalents (FTEs) over the 12 months of the year. The average workforce of Biotest was calculated as the average headcount over the 12 months of the year.
| AVERAGE WORKFORCE BY PROFESSIONAL GENDER AND WORKING HOURS | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | |||||||||
| Full time | Part time | Total | Full time | Part time | Total | Full time | Part time | Total | |||
| Women | 10,466 | 633 | 11,100 | 10,793 | 665 | 11,459 | 12,613 | 749 | 13,362 | ||
| Men | 8,220 | 243 | 8,463 | 8,248 | 265 | 8,513 | 8,778 | 283 | 9,062 | ||
| Undeclared | 33 | 74 | 107 | 46 | 1 | 47 | 25 | 1 | 26 | ||
| Other | 7 | 0 | 7 | ||||||||
| Total | 18,726 | 950 | 19,676 | 19,087 | 931 | 20,019 | 22,181 | 268 | 22,450 |
| AVERAGE WORKFORCE BY PROFESSIONAL GENDER AND WORKING HOURS - BIOTEST | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | |||||||||
| Full time | Part time | Total | Full time | Part time | Total | |||||
| Women | 976 | 290 | 1,266 | 935 | 387 | 1,322 | ||||
| Men | 1,148 | 54 | 1,202 | 1,084 | 82 | 1,166 | ||||
| Total | 2,124 | 344 | 2,468 | 2,018 | 469 | 2,487 |
| AVERAGE WORKFORCE BY WORKING HOURS AND AGE | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | |||||||||||
| <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | ||
| Full time | 4,645 | 9,951 | 4,130 | 18,726 | 4,871 | 10,071 | 4,145 | 19,087 | 5,818 | 11,244 | 4,355 | 21,417 | |
| Part time | 268 | 419 | 263 | 950 | 283 | 466 | 182 | 931 | 398 | 462 | 173 | 1,033 | |
| Total | 4,914 | 10,369 | 4,393 | 19,676 | 5,154 | 10,537 | 4,327 | 20,019 | 6,216 | 11,706 | 4,528 | 22,450 |
| AVERAGE WORKFORCE BY WORKING HOURS AND AGE - BIOTEST | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | ||||||||||
| <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | ||||
| Full time | 415 | 1,190 | 519 | 2,124 | 402 | 1,088 | 529 | 2,018 | |||
| Part time | 49 | 189 | 106 | 344 | 74 | 246 | 150 | 469 | |||
| Total | 464 | 1,379 | 625 | 2,468 | 476 | 1,333 | 679 | 2,487 |
| AVERAGE WORKFORCE BY TYPE OF CONTRACT AND AGE | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | |||||||||||
| <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | ||
| Permanent | 4,828 | 10,243 | 4,330 | 19,402 | 5,072 | 10,422 | 4,274 | 19,768 | 6,125 | 11,577 | 4,478 | 22,181 | |
| Temporary | 86 | 126 | 63 | 274 | 82 | 115 | 53 | 250 | 91 | 128 | 49 | 268 | |
| Total | 4,914 | 10,369 | 4,393 | 19,676 | 5,154 | 10,537 | 4,327 | 20,019 | 6,216 | 11,705 | 4,528 | 22,450 |
| AVERAGE WORKFORCE BY TYPE OF CONTRACT AND AGE - BIOTEST | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| 2023 | 2023 | ||||||||||
| <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | ||||
| Permanent | 418 | 1,334 | 612 | 2,363 | 412 | 1,259 | 664 | 2,335 | |||
| Temporary | 47 | 45 | 13 | 104 | 64 | 74 | 15 | 153 | |||
| Total | 464 | 1,379 | 625 | 2,468 | 476 | 1,333 | 679 | 2,487 |
| AVERAGE WORKFORCE BY PROFESSIONAL CATEGORY AND GENDER | ||
|---|---|---|
| 2024 | 2023 | 2022 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Women | Men | Undeclared | Other | Total | Women | Men | Undeclared/ Other |
Total | Women | Men | Undeclared/ Other |
Total | |
| Executives | 28.9% | 71.1% | 0.0% | 0.0% | 123 | 24.9% | 75.1% | 0.0% | 122 | 22.4% | 77.6% | 0.0% | 126 |
| Directors | 40.3% | 59.7% | 0.0% | 0.0% | 412 | 40.2% | 59.7% | 0.1% | 449 | 41.2% | 58.3% | 0.5% | 472 |
| Senior management | 43.0% | 57.0% | 0.0% | 0.0% | 562 | 41.5% | 58.5% | 0.0% | 556 | 39.2% | 60.8% | 0.0% | 572 |
| Management | 46.8% | 53.2% | 0.0% | 0.0% | 1,261 | 46.6% | 53.4% | 0.0% | 1,270 | 47.4% | 52.5% | 0.0% | 1,338 |
| Senior Professionals | 48.0% | 51.9% | 0.1% | 0.0% | 2,016 | 48.1% | 51.8% | 0.1% | 1,986 | 46.6% | 53.3% | 0.0% | 2,016 |
| Professionals | 52.5% | 47.3% | 0.1% | 0.0% | 2,646 | 52.7% | 47.2% | 0.1% | 2,700 | 52.3% | 47.6% | 0.1% | 2,753 |
| Administrative staff / Manufacturing operators |
60.9% | 38.2% | 0.8% | 0.1% | 12,656 | 62.2% | 37.5% | 0.3% | 12,936 | 65.3% | 34.6% | 0.1% | 15,172 |
| Total | 56.4% | 43.0% | 0.5% | 0.0% | 19,676 | 57.2% | 42.5% | 0.2% | 20,019 | 60.0% | 40.0% | 0.0% | 22,450 |
| 2024 | 2023 | ||||||
|---|---|---|---|---|---|---|---|
| Women | Men | Total | Women | Men | Total | ||
| Executives | 54.5% | 45.5% | 4 | 32.4% | 67.6% | 6 | |
| Directors | 29.2% | 70.8% | 36 | 30.2% | 69.8% | 33 | |
| Senior management | 33.5% | 66.5% | 68 | 32.3% | 67.7% | 68 | |
| Management | 58.0% | 42.0% | 114 | 57.6% | 42.4% | 144 | |
| Senior Professionals | 50.4% | 49.6% | 439 | 51.2% | 48.8% | 539 | |
| Professionals | 68.9% | 31.1% | 602 | 72.9% | 27.1% | 604 | |
| Administrative staff / Manufacturing operators | 43.8% | 56.2% | 1,205 | 44.7% | 55.3% | 1,094 | |
| Total | 51.3% | 48.7% | 2,468 | 53.1% | 46.9% | 2,487 |
| 2024 | 2023 | 2022 | |||||||
|---|---|---|---|---|---|---|---|---|---|
| Permanent | Temporary | Total | Permanent | Temporary | Total | Permanent | Temporary | Total | |
| Executives | 120 | 3 | 123 | 121 | 1 | 122 | 126 | 0 | 126 |
| Directors | 410 | 2 | 412 | 445 | 4 | 449 | 469 | 3 | 472 |
| Senior management | 557 | 5 | 562 | 553 | 3 | 556 | 568 | 4 | 572 |
| Management | 1,251 | 10 | 1,261 | 1,260 | 11 | 1,270 | 1,331 | 7 | 1,338 |
| Senior Professionals | 1,998 | 18 | 2,016 | 1,968 | 17 | 1,986 | 1,998 | 19 | 2,016 |
| Professionals | 2,604 | 42 | 2,646 | 2,656 | 44 | 2,700 | 2,692 | 61 | 2,753 |
| Administrative staff / Manufacturing operators | 12,462 | 194 | 12,656 | 12,766 | 170 | 12,936 | 14,997 | 175 | 15,172 |
| Total | 19,402 | 274 | 19,676 | 19,769 | 250 | 20,019 | 22,181 | 268 | 22,450 |
| 2024 | 2023 | ||||||
|---|---|---|---|---|---|---|---|
| Permanent | Temporary | Total | Permanent | Temporary | Total | ||
| Executives | 4 | 0 | 4 | 6 | 0 | 6 | |
| Directors | 36 | 0 | 36 | 33 | 0 | 33 | |
| Senior management | 68 | 0 | 68 | 68 | 0 | 68 | |
| Management | 112 | 2 | 114 | 139 | 5 | 144 | |
| Senior Professionals | 434 | 4 | 439 | 509 | 30 | 539 | |
| Professionals | 561 | 41 | 602 | 550 | 54 | 604 | |
| Administrative staff / Manufacturing operators | 1,148 | 57 | 1,205 | 1,030 | 64 | 1,094 | |
| Total | 2,363 | 104 | 2,468 | 2,335 | 153 | 2,487 |
| GRIFOLS | |
|---|---|
| --------- | -- |
| AVERAGE WORKFORCE BY PROFESSIONAL CATEGORY AND WORKING HOURS | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | |||||||||
| Full time | Part time | Total | Full time | Part time | Total | Full time | Part time | Total | |||
| Executives | 119 | 5 | 123 | 119 | 3 | 122 | 122 | 4 | 126 | ||
| Directors | 402 | 11 | 412 | 435 | 14 | 449 | 455 | 17 | 472 | ||
| Senior management | 555 | 7 | 562 | 546 | 10 | 556 | 558 | 14 | 572 | ||
| Management | 1,227 | 34 | 1,261 | 1,224 | 46 | 1,270 | 1,294 | 44 | 1,338 | ||
| Senior Professionals | 1,964 | 52 | 2,016 | 1,928 | 58 | 1,986 | 1,949 | 67 | 2,016 | ||
| Professionals | 2,551 | 95 | 2,646 | 2,595 | 105 | 2,700 | 2,668 | 84 | 2,753 | ||
| Administrative staff / Manufacturing operators | 11,910 | 747 | 12,656 | 12,241 | 695 | 12,936 | 14,370 | 802 | 15,172 | ||
| Total | 18,726 | 950 | 19,676 | 19,087 | 931 | 20,019 | 21,417 | 1,033 | 22,450 |
| 2024 | 2023 | |||||
|---|---|---|---|---|---|---|
| Full time | Part time | Total | Full time | Part time | Total | |
| Executives | 4 | 0 | 4 | 6 | 0 | 6 |
| Directors | 34 | 2 | 36 | 31 | 2 | 33 |
| Senior management | 58 | 10 | 68 | 57 | 11 | 68 |
| Management | 98 | 15 | 114 | 120 | 24 | 144 |
| Senior Professionals | 363 | 76 | 439 | 422 | 117 | 539 |
| Professionals | 474 | 128 | 602 | 465 | 140 | 604 |
| Administrative staff / Manufacturing operators | 1,093 | 113 | 1,205 | 918 | 175 | 1,094 |
| Total | 2,124 | 344 | 2,468 | 2,018 | 469 | 2,487 |
| 2024 | 2023 | 2022 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | ||
| Executives | 0.0% | 44.7% | 55.3% | 123 | 0.0% | 41.8% | 58.2% | 122 | 0.0% | 36.9% | 63.1% | 126 | |
| Directors | 0.0% | 45.5% | 54.5% | 412 | 0.2% | 46.6% | 53.2% | 449 | 0.4% | 45.5% | 54.1% | 472 | |
| Senior management | 0.5% | 54.6% | 44.9% | 562 | 0.5% | 54.9% | 44.6% | 556 | 0.6% | 54.2% | 45.2% | 572 | |
| Management | 2.5% | 64.1% | 33.4% | 1,261 | 3.0% | 64.7% | 32.2% | 1,270 | 3.0% | 65.5% | 31.6% | 1,338 | |
| Senior Professionals | 8.3% | 63.8% | 28.0% | 2,016 | 8.6% | 63.1% | 28.4% | 1,986 | 8.5% | 64.5% | 27.0% | 2,016 | |
| Professionals | 12.8% | 64.6% | 22.6% | 2,646 | 13.7% | 64.6% | 21.7% | 2,700 | 13.9% | 65.5% | 20.5% | 2,753 | |
| Administrative staff / Manufacturing operators |
34.6% | 47.5% | 17.9% | 12,656 | 35.4% | 47.6% | 17.1% | 12,936 | 37.0% | 47.2% | 15.8% | 15,172 | |
| Total | 25.0% | 52.7% | 22.3% | 19,676 | 25.7% | 52.6% | 21.6% | 20,019 | 27.7% | 52.1% | 20.2% | 22,450 |
| 2024 | ||||||||
|---|---|---|---|---|---|---|---|---|
| <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | |
| Executives | 0.0% | 27.3% | 72.8% | 4 | 0.0% | 33.8% | 66.2% | 6 |
| Directors | 0.0% | 44.2% | 55.8% | 36 | 0.0% | 30.5% | 69.5% | 33 |
| Senior management | 0.0% | 43.9% | 56.1% | 68 | 1.0% | 40.9% | 58.2% | 68 |
| Management | 0.7% | 57.4% | 41.9% | 114 | 1.5% | 51.7% | 46.9% | 144 |
| Senior Professionals | 7.3% | 68.7% | 31.3% | 439 | 8.2% | 65.1% | 26.7% | 539 |
| Professionals | 18.0% | 60.4% | 21.6% | 602 | 20.2% | 58.2% | 21.6% | 604 |
| Administrative staff / Manufacturing operators |
26.8% | 51.7% | 21.5% | 1,205 | 28.0% | 47.3% | 24.7% | 1,094 |
| Total | 18.8% | 55.9% | 25.3% | 2,468 | 19.1% | 53.6% | 27.3% | 2,487 |
| GRIFOLS | |
|---|---|
| --------- | -- |
| AVERAGE WORKFORCE BY COUNTRY AND GENDER | |||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | |||||||||||||
| Women | Men | Undeclared | Other | Total | Women | Men | Undeclared/ Other |
Total | Women | Men | Undeclared/ Other |
Total | |||
| U.S. | 7,512 | 4,937 | 107 | 7 | 12,563 | 8,000 | 5,106 | 38 | 13,143 | 9,965 | 5,679 | 26 | 15,644 | ||
| Spain | 1,900 | 2,327 | 0 | 0 | 4,227 | 1,818 | 2,275 | 1 | 4,095 | 1,798 | 2,284 | 0 | 4,082 | ||
| Germany | 957 | 403 | 0 | 0 | 1,360 | 1,641 | |||||||||
| RoW | 730 | 796 | 0 | 0 | 1,526 | 1,132 | 8 | 2,781 | 1,599 | 1,099 | 0 | 2,699 | |||
| Total | 11,099 | 8,463 | 107 | 7 | 19,676 | 11,459 | 8,513 | 47 | 20,019 | 13,362 | 9,062 | 26 | 22,450 |
| AVERAGE WORKFORCE BY COUNTRY AND GENDER - BIOTEST | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | ||||||||
| Women | Men | Total | Women | Men | Total | ||||
| Germany | 875 | 1,091 | 1,966 | 904 | 1,046 | 1,950 | |||
| RoW | 391 | 111 | 501 | 418 | 119 | 537 | |||
| Total | 1,266 | 1,202 | 2,468 | 1,322 | 1,166 | 2,487 |
| WORKFORCE DISTRIBUTION BY COUNTRY | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| 2024 | % | 2023 | % | 2022 | % | ||||
| U.S. | 13,534 | 64.0% | 13,918 | 65.8% | 16,734 | 69.9% | |||
| Spain | 4,408 | 20.8% | 4,181 | 19.8% | 4,217 | 17.6% | |||
| Germany | 1,571 | 7.4% | |||||||
| RoW | 1,643 | 7.8% | 3,045 | 14.4% | 2,996 | 12.5% | |||
| Total | 21,156 | 100.0% | 21,144 | 100.0% | 23,947 | 100.0% |
| WORKFORCE DISTRIBUTION BY COUNTRY - BIOTEST | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| 2024 | % | 2023 | % | 2022 | % | ||||
| Germany | 2,139 | 80.2% | 2,045 | 78.7% | 1,796 | 75.9% | |||
| RoW | 527 | 19.8% | 552 | 21.3% | 564 | 23.8% | |||
| Total | 2,666 | 100.0% | 2,597 | 100.0% | 2,367 | 100.0% |
| WORKFORCE DISTRIBUTION BY AGE | |||
|---|---|---|---|
| 2024 | 2023 | 2022 | |
| <30 | 5,600 | 5,702 | 6,859 |
| 30-50 | 10,959 | 10,931 | 12,241 |
| >50 | 4,597 | 4,511 | 4,847 |
| Total | 21,156 | 21,144 | 23,947 |
| WORKFORCE DISTRIBUTION BY AGE - BIOTEST | |||
|---|---|---|---|
| 2024 | 2023 | 2022 | |
| <30 | 503 | 506 | 434 |
| 30-50 | 1,478 | 1,393 | 1,272 |
| >50 | 685 | 698 | 661 |
| Total | 2,666 | 2,597 | 2,367 |
| WORKFORCE DISTRIBUTION BY REGION AND TYPE OF CONTRACT | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | ||||||||
| Permanent | Temporary | Total | Permanent | Temporary | Total | Permanent | Temporary | Total | ||
| U.S. | 13,531 | 3 | 13,534 | 13,914 | 4 | 13,918 | 16,725 | 9 | 16,734 | |
| Europe | 6,644 | 358 | 7,002 | 6,402 | 280 | 6,682 | 6,356 | 318 | 6,674 | |
| RoW | 614 | 6 | 620 | 534 | 10 | 544 | 530 | 9 | 539 | |
| Total | 20,789 | 367 | 21,156 | 20,850 | 294 | 21,144 | 23,611 | 336 | 23,947 | |
| % | 98.3% | 1.7% | 100.0% | 99% | 1% | 100% | 98.6% | 1.4% | 100.0% |
| WORKFORCE DISTRIBUTION BY REGION AND TYPE OF CONTRACT - BIOTEST | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | |||||||
| Permanent | Temporary | Total | Permanent | Temporary | Total | Permanent | Temporary | Total | |
| Europe | 2,522 | 144 | 2,666 | 2,432 | 165 | 2,597 | 2,156 | 209 | 2,365 |
| RoW | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 0 | 2 |
| Total | 2,522 | 144 | 2,666 | 2,432 | 165 | 2,597 | 2,158 | 209 | 2,367 |
| % | 94.6% | 5.4% | 100.0% | 94% | 6% | 100% | 91% | 9% | 100% |
| WORKFORCE DISTRIBUTION BY GENDER AND TYPE OF CONTRACT | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | ||||||||
| Permanent | Temporary | Total | Permanent | Temporary | Total | Permanent | Temporary | Total | ||
| Women | 11,939 | 206 | 12,145 | 12,096 | 163 | 12,259 | 14,206 | 182 | 14,388 | |
| Men | 8,792 | 161 | 8,953 | 8,695 | 131 | 8,826 | 9,366 | 154 | 9,520 | |
| Undeclared | 50 | 0 | 50 | |||||||
| Other | 8 | 0 | 8 | 59 | 0 | 59 | 39 | 0 | 39 | |
| Total | 20,789 | 367 | 21,156 | 20,850 | 294 | 21,144 | 23,611 | 336 | 23,947 | |
| % | 98.3% | 1.7% | 100.0% | 98.6% | 1.4% | 100.0% | 98.6% | 1.4% | 100.0% |
| 2024 | 2023 | 2022 | |||||||
|---|---|---|---|---|---|---|---|---|---|
| Permanent | Temporary | Total | Permanent | Temporary | Total | Permanent | Temporary | Total | |
| Women | 1,298 | 99 | 1,397 | 1,247 | 134 | 1,381 | 1,112 | 157 | 1,269 |
| Men | 1,224 | 45 | 1,269 | 1,185 | 31 | 1,216 | 1,046 | 52 | 1,098 |
| Total | 2,522 | 144 | 2,666 | 2,432 | 165 | 2,597 | 2,158 | 209 | 2,367 |
| % | 94.6% | 5.4% | 100.0% | 93.6% | 6.4% | 100.0% | 91.2% | 8.8% | 100.0% |
| WORKFORCE DISTRIBUTION BY GENDER AND WORKING HOURS | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | |||||||||
| Full time | Part time | Total | Full time | Part time | Total | Full time | Part time | Total | |||
| Women | 11,181 | 964 | 12,145 | 11,266 | 993 | 12,259 | 13,266 | 1,122 | 14,388 | ||
| Men | 8,625 | 328 | 8,953 | 8,505 | 321 | 8,826 | 9,168 | 352 | 9,520 | ||
| Undeclared | 46 | 4 | 50 | ||||||||
| Other | 8 | 0 | 8 | 56 | 3 | 59 | 36 | 3 | 39 | ||
| Total | 19,860 | 1,296 | 21,156 | 19,827 | 1,317 | 21,144 | 22,470 | 1,477 | 23,947 | ||
| % | 93.9% | 6.1% | 100.0% | 93.8% | 6.2% | 100.0% | 93.8% | 6.2% | 100.0% |
| GRIFOLS | |
|---|---|
| -- | --------- |
| WORKFORCE DISTRIBUTION BY GENDER AND WORKING HOURS - BIOTEST | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | |||||||||
| Full time | Part time | Total | Full time | Part time | Total | Full time | Part time | Total | |||
| Women | 986 | 411 | 1,397 | 984 | 397 | 1,381 | 912 | 357 | 1,269 | ||
| Men | 1,169 | 100 | 1,269 | 1,124 | 92 | 1,216 | 1,030 | 68 | 1,098 | ||
| Total | 2,155 | 511 | 2,666 | 2,108 | 489 | 2,597 | 1,942 | 425 | 2,367 | ||
| % | 80.8% | 19.2% | 100.0% | 81.2% | 18.8% | 100.0% | 82.0% | 18.0% | 100.0% |
| WORKFORCE DISTRIBUTION BY WORKING HOURS AND AGE | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | ||||||||||
| <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | |
| Full time | 5,127 | 10,405 | 4,328 | 19,860 | 5,196 | 10,363 | 4,268 | 19,827 | 6,243 | 11,648 | 4,579 | 22,470 |
| Part time | 473 | 554 | 269 | 1,296 | 506 | 568 | 243 | 1,317 | 616 | 593 | 268 | 1,477 |
| Total | 5,600 | 10,959 | 4,597 | 21,156 | 5,702 | 10,931 | 4,511 | 21,144 | 6,859 | 12,241 | 4,847 | 23,947 |
| WORKFORCE DISTRIBUTION BY WORKING HOURS AND AGE - BIOTEST | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | ||||||||||
| <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | |
| Full time | 409 | 1,217 | 529 | 2,155 | 426 | 1,140 | 542 | 2,108 | 377 | 1,044 | 521 | 1,942 |
| Part time | 94 | 261 | 156 | 511 | 80 | 253 | 156 | 489 | 57 | 228 | 140 | 425 |
| Total | 503 | 1,478 | 685 | 2,666 | 506 | 1,393 | 698 | 2,597 | 434 | 1,272 | 661 | 2,367 |
| WORKFORCE DISTRIBUTION BY TYPE OF CONTRACT AND AGE | ||||
|---|---|---|---|---|
| -- | ---------------------------------------------------- | -- | -- | -- |
| 2024 | 2023 | 2022 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | |
| Permanent | 5,496 | 10,815 | 4,478 | 20,789 | 5,628 | 10,814 | 4,408 | 20,850 | 6,763 | 12,113 | 4,735 | 23,611 |
| Temporary | 104 | 144 | 119 | 367 | 74 | 117 | 103 | 294 | 96 | 128 | 112 | 336 |
| Total | 5,600 | 10,959 | 4,597 | 21,156 | 5,702 | 10,931 | 4,511 | 21,144 | 6,859 | 12,241 | 4,847 | 23,947 |
| 2024 | 2023 | 2022 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | |
| Permanent | 436 | 1,425 | 661 | 2,522 | 434 | 1,318 | 680 | 2,432 | 346 | 1,173 | 639 | 2,158 |
| Temporary | 67 | 53 | 24 | 144 | 72 | 75 | 18 | 165 | 88 | 99 | 22 | 209 |
| Total | 503 | 1,478 | 685 | 2,666 | 506 | 1,393 | 698 | 2,597 | 434 | 1,272 | 661 | 2,367 |
| 2024 | 2023 | 2022 | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Women | Men | Undeclared | Other | Total | Women | Men | Undeclared/ Other |
Total | Women | Men | Undeclared/ Other |
Total | ||
| Executives | 28.0% | 72.0% | 0.0% | 0.0% | 118 | 23.3% | 76.7% | 0.0% | 120 | 23.8% | 76.2% | 0.0% | 122 | |
| Directors | 40.7% | 59.3% | 0.0% | 0.0% | 440 | 38.8% | 61.2% | 0.0% | 443 | 40.7% | 58.9% | 0.4% | 484 | |
| Senior management | 43.1% | 56.9% | 0.0% | 0.0% | 582 | 41.6% | 58.4% | 0.0% | 553 | 38.8% | 61.2% | 0.0% | 565 | |
| Management | 46.8% | 53.2% | 0.1% | 0.0% | 1,300 | 47.0% | 53.0% | 0.0% | 1,266 | 47.1% | 52.7% | 0.1% | 1,337 | |
| Senior Professionals | 48.6% | 51.4% | 0.0% | 0.0% | 2,098 | 48.3% | 51.6% | 0.1% | 1,975 | 47.4% | 52.6% | 0.0% | 2,054 | |
| Professionals | 53.5% | 46.3% | 0.2% | 0.0% | 2,737 | 52.7% | 47.2% | 0.1% | 2,701 | 52.4% | 47.6% | 0.1% | 2,799 | |
| Administrative staff | ||||||||||||||
| / Manufacturing | 61.9% | 37.7% | 0.3% | 0.1% | 13,881 | 62.9% | 36.7% | 0.4% | 14,086 | 65.6% | 34.2% | 0.2% | 16,586 | |
| operators | ||||||||||||||
| Total | 57.4% | 42.3% | 0.2% | 0.0% | 21,156 | 58.0% | 41.7% | 0.3% | 21,144 | 60.1% | 39.8% | 0.2% | 23,947 |
| 2024 | 2023 | 2022 | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Women | Men | Total | Women | Men | Total | Women | Men | Total | ||
| Executives | 66.7% | 33.3% | 3 | 33.3% | 66.7% | 6 | 29.7% | 70.3% | 37 | |
| Directors | 31.4% | 68.6% | 35 | 29.4% | 70.6% | 34 | 46.9% | 53.1% | 209 | |
| Senior management | 32.9% | 67.1% | 70 | 32.9% | 67.1% | 70 | 52.7% | 47.3% | 311 | |
| Management | 56.7% | 43.3% | 127 | 58.3% | 41.7% | 144 | 53.4% | 46.6% | 191 | |
| Senior Professionals | 52.9% | 47.1% | 478 | 52.1% | 47.9% | 562 | 55.2% | 44.8% | 279 | |
| Professionals | 70.5% | 29.5% | 672 | 72.7% | 27.3% | 626 | 80.6% | 19.4% | 330 | |
| Administrative staff / Manufacturing operators |
43.9% | 56.1% | 1,281 | 44.5% | 55.5% | 1,155 | 46.9% | 53.1% | 1,010 | |
| Total | 52.4% | 47.6% | 2,666 | 53.2% | 46.8% | 2,597 | 53.6% | 46.4% | 2,367 |
| 2024 | 2023 | 2022 | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Permanent | Temporary | Total | Permanent | Temporary | Total | Permanent | Temporary | Total | ||
| Executives | 113 | 5 | 118 | 115 | 5 | 120 | 121 | 1 | 122 | |
| Directors | 438 | 2 | 440 | 440 | 3 | 443 | 481 | 3 | 484 | |
| Senior management | 576 | 6 | 582 | 547 | 6 | 553 | 559 | 6 | 565 | |
| Management | 1,282 | 18 | 1,300 | 1,248 | 18 | 1,266 | 1,318 | 19 | 1,337 | |
| Senior Professionals | 2,075 | 23 | 2,098 | 1,955 | 20 | 1,975 | 2,033 | 21 | 2,054 | |
| Professionals | 2,685 | 52 | 2,737 | 2,647 | 54 | 2,701 | 2,728 | 71 | 2,799 | |
| Administrative staff / Manufacturing operators |
13,620 | 261 | 13,881 | 13,898 | 188 | 14,086 | 16,371 | 215 | 16,586 | |
| Total | 20,789 | 367 | 21,156 | 20,850 | 294 | 21,144 | 23,611 | 336 | 23,947 |
| 2024 | 2023 | 2022 | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Permanent | Temporary | Total | Permanent | Temporary | Total | Permanent | Temporary | Total | ||
| Executives | 3 | 0 | 3 | 6 | 0 | 6 | 37 | 0 | 37 | |
| Directors | 34 | 1 | 35 | 34 | 0 | 34 | 203 | 6 | 209 | |
| Senior management | 70 | 0 | 70 | 69 | 1 | 70 | 281 | 30 | 311 | |
| Management | 124 | 3 | 127 | 140 | 4 | 144 | 181 | 10 | 191 | |
| Senior Professionals | 473 | 5 | 478 | 530 | 32 | 562 | 262 | 17 | 279 | |
| Professionals | 617 | 55 | 672 | 560 | 66 | 626 | 278 | 52 | 330 | |
| Administrative staff / Manufacturing operators |
1,201 | 80 | 1,281 | 1,093 | 62 | 1,155 | 916 | 94 | 1,010 | |
| Total | 2,522 | 144 | 2,666 | 2,432 | 165 | 2,597 | 2,158 | 209 | 2,367 |
| 2024 | 2023 | 2022 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | |
| Executives | 0.0% | 40.7% | 59.3% | 118 | 0.0% | 40.8% | 59.2% | 120 | 0.0% | 36.9% | 63.1% | 122 |
| Directors | 0.0% | 43.9% | 56.1% | 440 | 0.0% | 44.7% | 55.3% | 443 | 0.2% | 44.0% | 55.8% | 484 |
| Senior management |
0.3% | 53.6% | 46.1% | 582 | 0.2% | 55.5% | 44.3% | 553 | 0.4% | 54.0% | 45.7% | 565 |
| Management | 2.4% | 64.2% | 33.4% | 1,300 | 2.7% | 64.1% | 33.3% | 1,266 | 2.2% | 64.9% | 32.8% | 1,337 |
| Senior Professionals |
8.3% | 63.9% | 27.7% | 2,098 | 7.8% | 63.4% | 28.8% | 1,975 | 7.9% | 64.0% | 28.1% | 2,054 |
| Professionals | 12.2% | 65.1% | 22.7% | 2,737 | 13.4% | 64.1% | 22.5% | 2,701 | 13.7% | 64.8% | 21.5% | 2,799 |
| Administrative staff / Manufacturing operators |
36.4% | 46.5% | 17.1% | 13,881 | 36.6% | 46.7% | 16.7% | 14,086 | 37.9% | 46.3% | 15.8% | 16,586 |
| Total | 26.5% | 51.8% | 21.7% | 21,156 | 27.0% | 51.7% | 21.3% | 21,144 | 28.6% | 51.1% | 20.2% | 23,947 |
2024 Non-Financial Information Statement and Sustainability reporting 109
| GRIFOLS | |
|---|---|
| -- | --------- |
| 2024 | 2023 | 2022 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | ||
| Executives | 0.0% | 33.3% | 66.7% | 3 | 0.0% | 33.3% | 66.7% | 6 | 0.0% | 32.4% | 67.6% | 37 | |
| Directors | 0.0% | 48.6% | 51.4% | 35 | 0.0% | 32.4% | 67.6% | 34 | 0.5% | 49.3% | 50.2% | 209 | |
| Senior management | 0.0% | 44.3% | 55.7% | 70 | 0.0% | 44.3% | 55.7% | 70 | 9.6% | 59.8% | 30.5% | 311 | |
| Management | 0.8% | 59.1% | 40.2% | 127 | 2.1% | 51.4% | 46.5% | 144 | 3.1% | 70.7% | 26.2% | 191 | |
| Senior Professionals | 9.0% | 61.3% | 29.7% | 478 | 9.1% | 64.1% | 26.9% | 562 | 14.3% | 68.1% | 17.6% | 279 | |
| Professionals | 16.8% | 60.9% | 22.3% | 672 | 20.9% | 57.7% | 21.4% | 626 | 23.9% | 52.4% | 23.6% | 330 | |
| Administrative staff / Manufacturing operators |
27.0% | 50.9% | 22.1% | 1,281 | 27.8% | 48.0% | 24.2% | 1,155 | 27.5% | 46.8% | 25.6% | 1,010 | |
| Total | 18.9% | 55.4% | 25.7% | 2,666 | 19.5% | 53.6% | 26.9% | 2,597 | 18.3% | 53.7% | 27.9% | 2,367 |
| 2024 | 2023 | 2022 | |||||||
|---|---|---|---|---|---|---|---|---|---|
| Full time | Part time | Total | Full time | Part time | Total | Full time | Part time | Total | |
| Executives | 118 | 0 | 118 | 118 | 2 | 120 | 122 | 0 | 122 |
| Directors | 414 | 26 | 440 | 416 | 27 | 443 | 449 | 35 | 484 |
| Senior management | 577 | 5 | 582 | 550 | 3 | 553 | 557 | 8 | 565 |
| Management | 1,270 | 30 | 1,300 | 1,234 | 32 | 1,266 | 1,303 | 34 | 1,337 |
| Senior Professionals | 2,058 | 40 | 2,098 | 1,936 | 39 | 1,975 | 2,001 | 53 | 2,054 |
| Professionals | 2,621 | 116 | 2,737 | 2,581 | 120 | 2,701 | 2,696 | 103 | 2,799 |
| Administrative staff / Manufacturing operators |
12,802 | 1,079 | 13,881 | 12,992 | 1,094 | 14,086 | 15,342 | 1,244 | 16,586 |
| Total | 19,860 | 1,296 | 21,156 | 19,827 | 1,317 | 21,144 | 22,470 | 1,477 | 23,947 |
| 2024 | 2023 | 2022 | |||||||
|---|---|---|---|---|---|---|---|---|---|
| Full time | Part time | Total | Full time | Part time | Total | Full time | Part time | Total | |
| Executives | 3 | 0 | 3 | 6 | 0 | 6 | 34 | 3 | 37 |
| Directors | 32 | 3 | 35 | 32 | 2 | 34 | 180 | 29 | 209 |
| Senior management | 60 | 10 | 70 | 57 | 13 | 70 | 229 | 82 | 311 |
| Management | 106 | 21 | 127 | 119 | 25 | 144 | 172 | 19 | 191 |
| Senior Professionals | 367 | 111 | 478 | 435 | 127 | 562 | 220 | 59 | 279 |
| Professionals | 481 | 191 | 672 | 485 | 141 | 626 | 260 | 70 | 330 |
| Administrative staff / Manufacturing operators |
1,106 | 175 | 1,281 | 974 | 181 | 1,155 | 847 | 163 | 1,010 |
| Total | 2,155 | 511 | 2,666 | 2,108 | 489 | 2,597 | 1,942 | 425 | 2,367 |
| 2024 | 2023 | 2022 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Women | Men Undeclared | Other | Total | Women | Men | Undeclared/ Other |
Total | Women | Men Undeclared/ Other |
Total | |||
| U.S. | 8,214 | 5,262 | 50 | 8 | 13,534 | 8,518 | 5,341 | 59 | 13,918 | 10,655 | 6,041 | 38 | 16,734 |
| Spain | 2,009 | 2,399 | 0 | 0 | 4,408 | 1,891 | 2,290 | 0 | 4,181 | 1,877 | 2,340 | 0 | 4,217 |
| Germany | 1,132 | 439 | 0 | 0 | 1,571 | 1,850 | 0 | 3,045 1,856 |
1,139 | 1 | 2,996 | ||
| RoW | 790 | 853 | 0 | 0 | 1,643 | 1,195 | |||||||
| Total | 12,145 | 8,953 | 50 | 8 | 21,156 | 12,259 | 8,826 | 59 | 21,144 | 14,388 | 9,520 | 39 | 23,947 |
| 2023 | 2022 | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| Women | Men | Total | Women | Men | Total | Women | Men | Total | |
| Germany | 980 | 1,159 | 2,139 | 949 | 1,096 | 2,045 | 840 | 956 | 1,796 |
| RoW | 417 | 110 | 527 | 432 | 120 | 552 | 424 | 140 | 564 |
| Total | 1,397 | 1,269 | 2,666 | 1,381 | 1,216 | 2,597 | 1,269 | 1,098 | 2,367 |
2024 Non-Financial Information Statement and Sustainability reporting 110

| NEW HIRES BY GENDER | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | |||||||||||
| Women | Men | Undeclared | Other | Total | Women | Men | Undeclared/ Other |
Total | Women | Men | Undeclared/ Other |
Total | |
| Total number of employees |
12,145 | 8,953 | 50 | 8 | 21,156 | 12,259 | 8,826 | 59 | 21,144 | 14,388 | 9,520 | 39 | 23,947 |
| Joiners7 | 3,933 | 2,098 | 50 | 2 | 6,083 | 4,160 | 2,037 | 49 | 6,246 | 8,296 | 3,208 | 64 | 11,568 |
| Ratio (joiners/ number of employees)8 |
32.4% | 23.4% | 100.0% | 25.0% | 28.8% | 33.9% | 23.1% | 83.1% | 29.5% | 57.7% | 33.7% | 164.1% | 48.3% |
| 2024 | 2023 | 2022 | |||||||
|---|---|---|---|---|---|---|---|---|---|
| Women | Men | Total | Women | Men | Total | Women | Men | Total | |
| Total number of employees | 1,266 | 1,202 | 2,468 | 1,322 | 1,165 | 2,487 | 1,269 | 1,098 | 2,367 |
| Joiners (FTE) 7 | 256 | 192 | 448 | 359 | 212 | 571 | 362 | 220 | 582 |
| Ratio (joiners/average number of employees) 9 |
20.2% | 16.0% | 18.2% | 27.2% | 18.2% | 23.0% | 28.5% | 20.0% | 24.6% |
| 2024 | 2023 | 2022 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | |
| Total number of employees |
5,600 | 10,959 | 4,597 | 21,156 | 5,702 | 10,931 | 4,511 | 21,144 | 6,859 | 12,241 | 4,847 | 23,947 |
| Joiners7 | 3,323 | 2,318 | 442 | 6,083 | 3,521 | 2,318 | 407 | 6,246 | 6,418 | 4,339 | 811 | 11,568 |
| Ratio (joiners/number of employees)8 |
59.3% | 21.2% | 9.6% | 28.8% | 61.8% | 21.2% | 9.0% | 29.5% | 93.6% | 35.4% | 16.7% | 48.3% |
| 2024 | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| <30 | 30-50 | >50 | Total | ||||||
| Total number of employees | 464 | 1,379 | 625 | 2,468 | |||||
| Joiners (FTE) 7 | 179 | 202 | 67 | 448 | |||||
| Ratio (joiners/number of employees)8 | 38.6% | 14.7% | 10.7% | 18.2% |
| 2024 | 2023 | 2022 | ||||||
|---|---|---|---|---|---|---|---|---|
| Joiners7 | Ratio (joiners/number of employees)8 |
Joiners7 | Ratio (joiners/number of employees)8 |
Joiners7 | Ratio (joiners/number of employees)8 |
|||
| U.S. | 4,736 | 35.0% | 5,168 | 37.1% | 10,339 | 61.8% | ||
| Europe | 1,200 | 17.1% | 970 | 14.5% | 1,136 | 1.7% | ||
| RoW | 147 | 23.7% | 108 | 19.9% | 93 | 17.3% | ||
| Total | 6,083 | 28.8% | 6,246 | 29.5% | 11,568 | 48.3% |
| 2024 | ||
|---|---|---|
| Joiners FTE7 | Ratio (joiners/average number of employees)9 | |
| Europe | 448 | 18.2% |
| RoW | 0 | 0.0% |
| Total | 448 | 18.2% |
Employees from acquisitions at the time of the transaction are not included as new hires. They are reflected as increases to the total workforce thereafter.
New hires are reported in headcount (HC), with the ratio calculated using the total workforce as the base.
New hires are reported in full-time equivalents (FTE), with the ratio calculated using the average workforce as the base.
| GRIFOLS | |
|---|---|
| --------- | -- |
| EMPLOYEE TURNOVER BY GENDER | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | |||||||||||
| Women | Men | Undeclared | Other | Total | Women | Men | Undeclared/ Other |
Total | Women | Men | Undeclared/ Other |
Total | |
| Total number of employees |
12,145 | 8,953 | 50 | 8 | 21,156 | 12,259 | 8,826 | 59 | 21,144 | 14,388 | 9,520 | 39 | 23,947 |
| Leavers | 4,402 | 2,038 | 38 | 2 | 6,480 | 6,165 | 2,695 | 34 | 8,894 | 7,666 | 2,885 | 31 | 10,582 |
| Ratio (leavers/ number of employees) |
36.2% | 22.8% | 76.0% | 25.0% | 30.6% | 50.3% | 30.5% | 57.6% | 42.1% | 53.3% | 30.3% | 79.5% | 44.2% |
| 2024 | 2023 | 2022 | |||||||
|---|---|---|---|---|---|---|---|---|---|
| Women | Men | Total | Women | Men | Total | Women | Men | Total | |
| Total number of employees | 1,397 | 1,269 | 2,666 | 1,381 | 1,216 | 2,597 | 1,269 | 1,098 | 2,367 |
| Leavers | 224 | 140 | 364 | 218 | 95 | 313 | 227 | 105 | 332 |
| Ratio (leavers/number of employees) | 16.0% | 11.0% | 13.7% | 15.8% | 7.8% | 12.1% | 17.9% | 9.6% | 14.0% |
| 2024 | 2023 | 2022 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | ||
| Total number of employees |
5,600 | 10,959 | 4,597 | 21,156 | 5,702 | 10,931 | 4,511 | 21,144 | 6,859 | 12,241 | 4,847 | 23,947 | |
| Leavers | 3,046 | 2,630 | 804 | 6,480 | 3,946 | 3,800 | 1,148 | 8,894 | 5,126 | 4,330 | 1,126 | 10,582 | |
| Ratio (leavers/ number of employees) |
54.4% | 24.0% | 17.5% | 30.6% | 69.2% | 34.8% | 25.4% | 42.1% | 74.7% | 35.4% | 23.2% | 44.2% |
| 2024 | ||||
|---|---|---|---|---|
| <30 | 30-50 | >50 | Total | |
| Total number of employees | 503 | 1,478 | 685 | 2,666 |
| Leavers | 110 | 170 | 84 | 364 |
| Ratio (leavers/number of employees) | 21.9% | 11.5% | 12.3% | 13.7% |
| 2024 | 2023 | 2022 | ||||
|---|---|---|---|---|---|---|
| Leavers | Ratio (leavers/ number of employees) |
Leavers | Ratio (leavers/ number of employees) |
Leavers | Ratio (leavers/ number of employees) |
|
| U.S. | 5,552 | 41.0% | 7,800 | 56.0% | 9,514 | 56.9% |
| Europe | 861 | 12.3% | 997 | 14.9% | 950 | 14.2% |
| RoW | 67 | 10.8% | 97 | 17.8% | 118 | 21.9% |
| Total | 6,480 | 30.6% | 8,894 | 42.1% | 10,582 | 44.2% |
| 2024 | ||
|---|---|---|
| Leavers | Ratio (leavers/number of employees) | |
| Europe | 364 | 13.7% |
| RoW | 0 | 0.0% |
| Total | 364 | 13.7% |
| GRIFOL | ||
|---|---|---|

| LEAVERS BY PROFESSIONAL CATEGORY | ||||
|---|---|---|---|---|
| 2024 | 2023 | 2022 | ||
| Executives | 25 | 27 | 26 | |
| Directors | 52 | 111 | 80 | |
| Senior management | 32 | 66 | 75 | |
| Management | 122 | 233 | 186 | |
| Senior Professionals | 200 | 312 | 308 | |
| Professionals | 351 | 564 | 537 | |
| Administrative staff / Manufacturing operators | 5,698 | 7,581 | 9,370 | |
| Total | 6,480 | 8,894 | 10,582 |
| LEAVERS BY PROFESSIONAL CATEGORY - BIOTEST | |||||
|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | |||
| Executives | 1 | 2 | 3 | ||
| Directors | 7 | 1 | 15 | ||
| Senior management | 7 | 7 | 43 | ||
| Management | 11 | 13 | 17 | ||
| Senior Professionals | 64 | 54 | 17 | ||
| Professionals | 81 | 65 | 60 | ||
| Administrative staff / Manufacturing operators | 193 | 171 | 177 | ||
| Total | 364 | 313 | 332 |
| 2024 | 2023 | 2022 | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Voluntary | Non-voluntary | Total | Voluntary | Non-voluntary | Total | Voluntary | Non-voluntary | Total | ||
| Executives | 6% | 15% | 21% | 8% | 14% | 23% | 7% | 15% | 21% | |
| Directors | 5% | 6% | 12% | 8% | 17% | 25% | 8% | 9% | 17% | |
| Senior management | 2% | 3% | 6% | 4% | 8% | 12% | 8% | 6% | 13% | |
| Management | 5% | 4% | 9% | 8% | 11% | 18% | 8% | 5% | 14% | |
| Senior Professional | 7% | 3% | 10% | 8% | 8% | 16% | 10% | 5% | 15% | |
| Professionals | 7% | 5% | 13% | 10% | 10% | 21% | 13% | 7% | 19% | |
| Administrative staff / Manufacturing operators |
29% | 12% | 41% | 36% | 18% | 54% | 47% | 19% | 56% | |
| Total | 21% | 10% | 31% | 27% | 15% | 42% | 36% | 9% | 44% |
| 2024 | 2023 | |||||||
|---|---|---|---|---|---|---|---|---|
| Voluntary | Non-voluntary | Total | Voluntary | Non-voluntary | Total | |||
| Executives | 0% | 0% | 0% | 33% | 0% | 33% | ||
| Directors | 2% | 0% | 2% | 3% | 0% | 3% | ||
| Senior management | 2% | 0% | 2% | 6% | 4% | 10% | ||
| Management | 3% | 0% | 3% | 6% | 3% | 9% | ||
| Senior Professional | 16% | 2% | 18% | 8% | 2% | 10% | ||
| Professionals | 19% | 3% | 22% | 9% | 1% | 10% | ||
| Administrative staff / Manufacturing operators | 37% | 10% | 47% | 11% | 3% | 15% | ||
| Total | 11% | 2% | 14% | 10% | 3% | 12% |
| DISMISSALS BY COUNTRY AND GENDER | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | ||||||||||||
| Women | Men Undeclared | Other | Total | Women | Men Undeclared/ Other |
Total | Women | Men Undeclared/ Other |
Total | |||||
| U.S. | 1,008 | 476 | 9 | 0 | 1,493 | 1,706 | 860 | 12 | 2,578 | 977 | 500 | 8 | 1,485 | |
| Spain | 29 | 43 | 0 | 0 | 72 | 55 | 79 | 0 | 134 | 25 | 40 | 0 | 65 | |
| Germany | 24 | 12 | 0 | 0 | 36 | |||||||||
| RoW | 25 | 33 | 0 | 0 | 58 | 105 | 66 | 0 | 171 | 52 | 23 | 0 | 75 | |
| Total | 1,086 | 564 | 9 | 0 | 1,659 | 1,866 | 1,005 | 12 | 2,883 | 1,054 | 563 | 8 | 1,625 | |
| % | 65.5% | 34.0% | 0.5% | 0.0% | 100.0% | 64.7% | 34.9% | 0.4% | 100.0% | 64.9% | 34.6% | 0.5% | 100.0% |
| DISMISSALS BY COUNTRY AND GENDER - BIOTEST | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | ||||||||||
| Women | Men | Total | Women | Men | Total | Women | Men | Total | ||||
| Germany | 23 | 18 | 41 | 29 | 20 | 49 | 14 | 17 | 31 | |||
| RoW | 16 | 7 | 23 | 16 | 1 | 17 | 25 | 6 | 31 | |||
| Total | 39 | 25 | 64 | 45 | 21 | 66 | 39 | 23 | 62 | |||
| % | 60.9% | 39.1% | 100.0% | 68.2% | 31.8% | 100.0% | 62.9% | 37.1% | 100.0% |
| DISMISSALS BY PROFESSIONAL CATEGORY AND COUNTRY | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | |||||||||
| U.S. | Spain | Germany | RoW | U.S. | Spain | RoW | U.S. | Spain | RoW | ||
| Executives | 1 | 9 | 0 | 2 | 9 | 3 | 0 | 10 | 2 | 0 | |
| Directors | 11 | 2 | 0 | 2 | 57 | 7 | 3 | 17 | 3 | 6 | |
| Senior management | 6 | 0 | 0 | 2 | 16 | 14 | 2 | 8 | 9 | 2 | |
| Management | 17 | 2 | 0 | 9 | 96 | 18 | 5 | 35 | 13 | 4 | |
| Senior Professionals | 27 | 3 | 0 | 3 | 83 | 24 | 14 | 53 | 9 | 5 | |
| Professionals | 71 | 5 | 10 | 13 | 169 | 21 | 41 | 114 | 6 | 13 | |
| Administrative staff / Manufacturing operators | 1,360 | 51 | 26 | 27 | 2,148 | 47 | 106 | 1,248 | 23 | 45 | |
| Total | 1,493 | 72 | 36 | 58 | 2,578 | 134 | 171 | 1,485 | 65 | 75 |
| DISMISSALS BY PROFESSIONAL CATEGORY AND COUNTRY - BIOTEST | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | |||||||||
| Germany | RoW | Germany | RoW | Germany | RoW | ||||||
| Executives | 0 | 0 | 0 | 0 | 1 | 0 | |||||
| Directors | 0 | 1 | 0 | 0 | 3 | 0 | |||||
| Senior management | 0 | 0 | 3 | 0 | 0 | 2 | |||||
| Management | 0 | 1 | 4 | 1 | 1 | 7 | |||||
| Senior Professionals | 5 | 1 | 7 | 2 | 1 | 0 | |||||
| Professionals | 1 | 10 | 3 | 6 | 1 | 12 | |||||
| Administrative staff / Manufacturing operators |
35 | 10 | 32 | 8 | 24 | 10 | |||||
| Total | 41 | 23 | 49 | 17 | 31 | 31 |
| GRIFOLS | |
|---|---|
| --------- | -- |
| DISMISSALS BY COUNTRY AND AGE | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | |||||||||||
| <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | ||
| U.S. | 676 | 657 | 160 | 1,493 | 962 | 1,226 | 390 | 2,578 | 606 | 680 | 199 | 1,485 | |
| Spain | 10 | 35 | 27 | 72 | 13 | 80 | 41 | 134 | 4 | 37 | 24 | 65 | |
| Germany | 10 | 15 | 11 | 36 | 171 | 14 | 34 | 27 | 75 | ||||
| RoW | 14 | 25 | 19 | 58 | 43 | 90 | 38 | ||||||
| Total | 710 | 732 | 217 | 1,659 | 1,018 | 1,396 | 469 | 2,883 | 624 | 751 | 250 | 1,625 | |
| % | 42.8% | 44.1% | 13.1% | 100.0% | 35.3% | 48.4% | 16.3% | 100.0% | 38.4% | 46.2% | 15.4% | 100.0% |
| 2024 | 2023 | 2022 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | <30 | 30-50 | >50 | Total | ||
| Germany | 8 | 19 | 14 | 41 | 17 | 14 | 18 | 49 | 11 | 13 | 7 | 31 | |
| RoW | 9 | 10 | 4 | 23 | 9 | 6 | 2 | 17 | 8 | 16 | 7 | 31 | |
| Total | 17 | 29 | 18 | 64 | 26 | 20 | 20 | 66 | 19 | 29 | 14 | 62 | |
| % | 26.6% | 45.3% | 28.1% | 100.0% | 39.4% | 30.3% | 30.3% | 100.0% | 30.6% | 46.8% | 22.6% | 100.0% |
| BREAKDOWN OF ABSEENTISM BY TYPE AND COUNTRY | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | |||||||||||
| U.S. | Spain | Germany | RoW | Total General |
U.S. | Spain | RoW | Total General |
U.S. | Spain | RoW | Total General |
|
| Illness | 445,410 | 390,266 | 273,437 | 31,609 | 1,140,722 | 564,089 | 344,969 | 291,370 | 1,200,427 | 586,913 | 380,924 | 315,499 | 1,283,336 |
| Work accident | 21,916 | 24,448 | 3,351 | 0 | 49,715 | 19,955 | 22,970 | 4,206 | 47,130 | 36,928 | 66,324 | 3,494 | 106,746 |
| Maternity / Paternity |
116,183 | 98,422 | 84,462 | 18,888 | 317,955 | 58,141 | 101,864 | 112,059 | 272,064 | 112,717 | 127,633 | 135,339 | 375,689 |
| Paid leave | 34,730 | 68,942 | 30,091 | 3,531 | 137,294 | 1,821 | 62,124 | 28,627 | 92,572 | 120,422 | 50,080 | 36,336 | 206,838 |
| Unpaid leave | 91,188 | 2,873 | 3,014 | 6,213 | 103,288 | 123,032 | 2,725 | 5,888 | 131,646 | 177,047 | 1,582 | 26,371 | 205,000 |
| Total | 709,427 | 584,951 | 394,355 | 60,241 | 1,748,974 | 767,038 | 534,652 | 442,150 | 1,743,839 | 1,034,027 | 626,543 | 517,040 | 2,177,610 |
| BREAKDOWN OF ABSEENTISM BY TYPE AND COUNTRY - BIOTEST | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2022 | ||||||||||
| Germany | RoW | Total | Germany | RoW | Total | Germany | |||||
| Illness | 316,293 | 37,554 | 353,847 | 265,158 | 29,752 | 294,910 | 239,233 | ||||
| Work accident | 4,151 | 264 | 4,415 | 1,855 | 568 | 2,423 | 4,269 | ||||
| Maternity / Paternity | 111,435 | 64,666 | 176,102 | 104,268 | 78,022 | 182,290 | 117,082 | ||||
| Paid leave | 59,391 | 80,997 | 140,388 | 49,479 | 81,165 | 130,644 | 104,505 | ||||
| Unpaid leave | 6,778 | 3,076 | 9,853 | 5,477 | 393 | 5,870 | 3,994 | ||||
| Total | 498,048 | 186,557 | 684,605 | 426,237 | 189,900 | 616,137 | 469,083 |
| 2024 | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Women | Men | Undeclared | Other | Total | Women % | Men % | Undeclared % | Other % | |
| Illness | 782,564 | 357,159 | 1,000 | 0 | 1,140,723 | 68.6% | 31.3% | 0.1% | 0.0% |
| Work accident | 30,752 | 18,963 | 0 | 0 | 49,715 | 61.9% | 38.1% | 0.0% | 0.0% |
| Maternity / Paternity | 220,969 | 96,895 | 91 | 0 | 317,955 | 69.5% | 30.5% | 0.0% | 0.0% |
| Paid leave | 77,303 | 59,931 | 24 | 36 | 137,294 | 56.3% | 43.7% | 0.0% | 0.0% |
| Unpaid leave | 62,175 | 41,113 | 0 | 0 | 103,288 | 60.2% | 39.8% | 0.0% | 0.0% |
| Total | 1,173,763 | 574,061 | 1,115 | 36 | 1,748,975 | 67.1% | 32.8% | 0.1% | 0.0% |
| 2023 | ||||||
|---|---|---|---|---|---|---|
| Women | Men | Undeclared/Other | Total | Women % | Men % | |
| Illness | 839,516 | 358,368 | 2,543 | 1,200,427 | 69.9% | 29.9% |
| Work accident | 20,016 | 27,114 | 0 | 47,130 | 42.5% | 57.5% |
| Maternity / Paternity | 192,076 | 79,846 | 143 | 272,064 | 70.6% | 29.3% |
| Paid leave | 50,834 | 41,735 | 3 | 92,572 | 54.9% | 45.1% |
| Unpaid leave | 79,661 | 51,984 | 0 | 131,646 | 60.5% | 39.5% |
| Total | 1,182,103 | 559,047 | 2,689 | 1,743,839 | 67.8% | 32.1% |
| 2022 | ||||||
|---|---|---|---|---|---|---|
| Women | Men | Undeclared/Other | Total | Women % | Men % | |
| Illness | 905,342 | 377,063 | 932 | 1,283,337 | 70.5% | 29.4% |
| Work accident | 65,402 | 41,345 | 0 | 106,747 | 61.3% | 38.7% |
| Maternity / Paternity | 298,566 | 77,123 | 0 | 375,689 | 79.5% | 20.5% |
| Paid leave | 134,921 | 71,836 | 80 | 206,837 | 65.2% | 34.7% |
| Unpaid leave | 141,841 | 63,159 | 0 | 205,000 | 69.2% | 30.8% |
| Total | 1,546,072 | 630,526 | 1,012 | 2,177,610 | 71.0% | 29.0% |
| 2024 | |||||
|---|---|---|---|---|---|
| Women | Men | Total | Women % | Men % | |
| Illness | 187,592 | 166,255 | 353,847 | 53.0% | 47.0% |
| Work accident | 1,616 | 2,799 | 4,415 | 36.6% | 63.4% |
| Maternity / Paternity | 160,641 | 15,461 | 176,102 | 91.2% | 8.8% |
| Paid leave | 85,345 | 55,043 | 140,388 | 60.8% | 39.2% |
| Unpaid leave | 4,513 | 5,340 | 9,853 | 45.8% | 54.2% |
| Total | 439,706 | 244,898 | 684,605 | 64.2% | 35.8% |
| 2023 | ||||||
|---|---|---|---|---|---|---|
| Women | Men | Total | Women % | Men % | ||
| Illness | 156,490 | 138,420 | 294,910 | 53.1% | 46.9% | |
| Work accident | 1,142 | 1,281 | 2,423 | 47.1% | 52.9% | |
| Maternity / Paternity | 171,822 | 10,469 | 182,290 | 94.3% | 5.7% | |
| Paid leave | 80,317 | 50,327 | 130,644 | 61.5% | 38.5% | |
| Unpaid leave | 2,243 | 3,627 | 5,870 | 38.2% | 61.8% | |
| Total | 412,013 | 204,124 | 616,137 | 66.9% | 33.1% |
| 2022 | ||||||
|---|---|---|---|---|---|---|
| Women | Men | Total | Women % | Men % | ||
| Illness | 116,069 | 123,164 | 239,233 | 48.5% | 51.5% | |
| Work accident | 554 | 3,715 | 4,269 | 13.0% | 87.0% | |
| Maternity / Paternity | 104,782 | 12,300 | 117,082 | 89.5% | 10.5% | |
| Paid leave | 37,850 | 66,655 | 104,505 | 36.2% | 63.8% | |
| Unpaid leave | 2,164 | 1,830 | 3,994 | 54.2% | 45.8% | |
| Total | 261,420 | 207,664 | 469,083 | 55.7% | 44.3% |
| 2024 | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Women | Men | Undeclared | Other | Total | Average training hours |
||||
| Executives | 458 | 1,870 | 0 | 0 | 2,328 | 19.7 | |||
| Directors | 6,717 | 9,135 | 0 | 0 | 15,852 | 36.0 | |||
| Senior management | 11,404 | 13,498 | 0 | 0 | 24,902 | 42.8 | |||
| Management | 27,849 | 30,032 | 0 | 0 | 57,881 | 44.5 | |||
| Senior Professionals | 49,104 | 58,086 | 43 | 0 | 107,233 | 51.1 | |||
| Professionals | 362,753 | 234,393 | 1,660 | 0 | 598,806 | 218.8 | |||
| Administrative staff / Manufacturing operators |
3,542,313 | 1,495,439 | 19,907 | 3,044 | 5,060,703 | 364.6 | |||
| Total | 4,000,598 | 1,842,453 | 21,610 | 3,044 | 5,867,705 | 277.4 | |||
| % by gender | 68.2% | 31.4% | 0.4% | 0.1% | 100.0% | ||||
| Average training hours per headcount |
329.4 | 205.8 | 432.2 | 380.5 | 277.4 | ||||
| Average training hours per FTE | 360.4 | 217.7 | 202.0 | 434.9 | 298.2 |

| 2023 | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Women | Men | Undeclared/ Other |
Total | Average training hours |
|||||
| Executives | 426 | 1,323 | 0 | 1,749 | 14.6 | ||||
| Directors | 5,315 | 8,876 | 10 | 14,201 | 32.1 | ||||
| Senior management | 9,945 | 12,615 | 0 | 22,560 | 40.8 | ||||
| Management | 29,269 | 35,574 | 0 | 64,843 | 51.2 | ||||
| Senior Professionals | 55,040 | 56,869 | 165 | 112,074 | 56.7 | ||||
| Professionals | 200,798 | 149,146 | 825 | 350,769 | 129.9 | ||||
| Administrative staff / Manufacturing operators | 3,529,520 | 1,469,488 | 17,374 | 5,016,382 | 356.1 | ||||
| Total | 3,830,313 | 1,733,891 | 18,374 | 5,582,578 | 264.0 | ||||
| % by gender | 68.6% | 31.1% | 0.3% | 100.0% | |||||
| Average training hours per headcount | 312.4 | 196.5 | 310.5 | 264.0 | |||||
| Average training hours per FTE | 347.5 | 210.0 | 481.0 | 289.0 |
| 2022 | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Women | Men | Undeclared/ Other |
Total | Average training hours |
|||||
| Executives | 512 | 1,349 | 0 | 1,861 | 15.3 | ||||
| Directors | 6,432 | 8,889 | 46 | 15,367 | 31.8 | ||||
| Senior management | 8,280 | 11,647 | 0 | 19,927 | 35.3 | ||||
| Management | 20,143 | 26,018 | 12 | 46,173 | 34.5 | ||||
| Senior Professionals | 46,076 | 56,366 | 17 | 102,459 | 49.9 | ||||
| Professionals | 102,709 | 92,304 | 434 | 195,447 | 69.8 | ||||
| Administrative staff / Manufacturing operators | 3,127,749 | 1,196,391 | 13,440 | 4,337,580 | 261.5 | ||||
| Total | 3,311,901 | 1,392,964 | 13,949 | 4,718,814 | 197.1 | ||||
| % by gender | 70.2% | 29.5% | 0.3% | 100.0% | |||||
| Average training hours per headcount | 230.2 | 146.3 | 357.7 | 197.1 | |||||
| Average training hours per FTE | 257.5 | 159.2 | 567.8 | 218.1 |
| 2024 | 2023 | 2022 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Women | Men | Total | Average training hours |
Women | Men | Total | Average training hours |
Women | Men | Total | Average training hours |
|
| Executives | 66 | 10 | 77 | 25.6 | 33 | 37 | 70 | 11.7 | 218 | 545 | 763 | 20.6 |
| Directors | 163 | 312 | 475 | 13.6 | 197 | 424 | 621 | 18.3 | 2,058 | 2,352 | 4,409 | 21.1 |
| Senior management | 348 | 757 | 1,104 | 15.8 | 329 | 1,028 | 1,357 | 19.4 | 3,673 | 3,000 | 6,673 | 21.5 |
| Management | 830 | 706 | 1,536 | 12.1 | 1,325 | 1,016 | 2,341 | 16.3 | 2,298 | 1,860 | 4,158 | 21.8 |
| Senior Professionals | 4,649 | 4,175 | 8,825 | 18.5 | 5,745 | 6,841 | 12,586 | 22.4 | 3,897 | 2,714 | 6,611 | 23.7 |
| Professionals | 7,355 | 3,560 | 10,915 | 16.2 | 8,526 | 3,753 | 12,279 | 19.6 | 6,919 | 1,392 | 8,311 | 25.2 |
| Administrative staff / Manufacturing operators |
12,604 | 16,834 | 29,438 | 23.0 | 10,881 | 18,700 | 29,580 | 25.6 | 1,025 | 10,749 | 20,775 | 20.6 |
| Total | 26,015 | 26,354 | 52,370 | 19.6 | 27,036 | 31,798 | 58,835 | 22.7 | 29,088 | 22,612 | 51,700 | 21.8 |
| % by gender | 49.7% | 50.3% | 100.0% | 46.0% | 54.0% | 100.0% | 56.3% | 43.7% | 100.0% | |||
| Average training hours per headcount |
18.6 | 20.8 | 19.6 | 19.6 | 26.1 | 22.7 | 22.6 | 20.5 | 21.6 | |||
| Average training hours per FTE |
20.6 | 21.9 | 21.2 | 20.5 | 27.3 | 23.7 | ND | ND | ND |


| 2024 | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Women | Men | Undeclared | Other | Total | Training days per employee |
% of employees that received training |
|||
| U.S. | 3,712,037 | 1,586,542 | 21,609 | 3,044 | 5,323,232 | 31.45 | 96.9% | ||
| Spain | 156,362 | 180,140 | 0 | 0 | 336,502 | 1.99 | 96.4% | ||
| Germany | 106,877 | 42,431 | 0 | 0 | 149,308 | 0.88 | 98.6% | ||
| RoW | 25,323 | 33,339 | 0 | 0 | 58,662 | 0.35 | 90.8% | ||
| Total | 4,000,599 | 1,842,452 | 21,609 | 3,044 | 5,867,704 | 34.67 | NA |
| 2023 | ||||||||
|---|---|---|---|---|---|---|---|---|
| Women | Men | Undeclared/Other | Total | Training days per employee |
% of employees that received training |
|||
| U.S. | 3,481,344 | 1,462,761 | 18,322 | 4,962,428 | 29.34 | 94.4% | ||
| Spain | 132,220 | 171,070 | 0 | 303,291 | 1.79 | 96.5% | ||
| RoW | 216,748 | 100,109 | 0 | 316,857 | 1.87 | 91.8% | ||
| Total | 3,830,312 | 1,733,940 | 18,322 | 5,582,576 | 33.00 | NA |
| Women | Men | Undeclared/Other | Total | |
|---|---|---|---|---|
| U.S. | 3,105,514 | 1,190,597 | 13,949 | 4,310,060 |
| Spain | 115,414 | 153,995 | 0 | 269,409 |
| RoW | 90,972 | 48,373 | 0 | 139,345 |
| Total | 3,311,900 | 1,392,965 | 13,949 | 4,718,814 |
| 2024 | 2023 | 2022 | |||||||
|---|---|---|---|---|---|---|---|---|---|
| Women | Men | Total | Women | Men | Total | Women | Men | Total | |
| Germany | 18,050 | 24,182 | 42,232 | 20,626 | 29,701 | 50,327 | 16,649 | 18,948 | 35,597 |
| RoW | 7,965 | 2,172 | 10,137 | 6,410 | 2,097 | 8,507 | 12,062 | 3,584 | 15,645 |
| Total | 26,015 | 26,354 | 52,369 | 27,036 | 31,798 | 58,835 | 29,088 | 22,612 | 51,700 |
| BREAKDOWN IN TRAINING HOURS IN HEALTH AND SAFETY AND ENVIRONMENT |
BREAKDOWN IN TRAINING HOURS IN HEALTH AND SAFETY AND ENVIRONMENT - BIOTEST |
||||||
|---|---|---|---|---|---|---|---|
| 2024 | 2023 | 2022 | 2024 | 2023 | 2022 | ||
| Total | 46,542 | 96,759 | 170,240 | Total | 8,132 | 5,758 | 5,230 |
| 2024 | 2023 | 2022 | |
|---|---|---|---|
| Executives | 100.0% | 88.9% | 41.9% |
| Directors | 99.8% | 99.4% | 81.8% |
| Senior management | 99.4% | 99.2% | 86.5% |
| Management | 99.7% | 99.6% | 89.1% |
| Senior Professionals | 99.9% | 99.5% | 88.5% |
| Professionals | 99.6% | 99.4% | 88.2% |
| Administrative staff / Manufacturing operators |
99.8% | 99.3% | 83.6% |
| Total | 99.8% | 99.2% | 86.0% |
PERCENTAGE OF EMPLOYEES RECEIVING REGULAR PERFORMANCE AND CAREER DEVELOPMENT REVIEWS
Women 99.7% 99.4% 85.2% Men 99.9% 99.4% 87.1%
Total 99.8% 99.2% 86.0%
2024 2023 2022
0.0% 50.0%
| 2024 | 2023 | |
|---|---|---|
| Executives | NA | 100% |
| Directors | NA | 94% |
| Senior management | NA | 100% |
| Management | NA | 94% |
| Senior Professionals | NA | 92% |
| Professionals | NA | 85% |
| Administrative staff / Manufacturing operators |
NA | 94% |
| Total | NA | 91% |
There is no information available regarding Biotest's performance reviews for 2024.
| 2024 | 2023 | |
|---|---|---|
| Women | NA | 86.1% |
| Men | NA | 97.5% |
| Total | NA | 91.4% |
There is no information available regarding Biotest's performance reviews for 2024.
Undeclared 0.0%
Other 100.0%
BY GENDER
| 2024 | 2023 | 2022 | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Women | Men | Undeclared | Other | Total | Women | Men | Total | Women | Men | Total | |
| Nº employees that were entitled to parental leave |
100% | 100% | 100% | 100% | 100% | 100% | 100% | 100% | 100% | 100% | 100% |
| Nº employees that took parental leave |
435 | 307 | 1 | 0 | 743 | 284 | 234 | 518 | 405 | 238 | 643 |
| Nº employees that returned to work in the reporting period after parental leave ended |
314 | 231 | 0 | 0 | 545 | 226 | 167 | 393 | 465 | 245 | 710 |
| Return to work rate | 69% | 88% | 0% | 0% | 76% | 74% | 89% | 79% | 83% | 94% | 87% |
| Total number of employees that returned to work after parental leave ended that were still employed 12 months after their return to work |
161 | 137 | 1 | 0 | 299 | 237 | 184 | 421 | 246 | 160 | 406 |
| Retention rate | 71% | 82% | 0% | 0% | 76% | 61% | 80% | 68% | 56% | 80% | 64% |
| GRIFOLS | |
|---|---|
| --------- | -- |
| PARENTAL LEAVE AND RETURN TO WORK - BIOTEST | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| 2024 | 2023 | ||||||||
| Women | Men | Total | Women | Men | Total | ||||
| Nº employees that were entitled to parental leave |
100% | 100% | 100% | 100% | 100% | 100% | |||
| Nº employees that took parental leave |
157 | 52 | 209 | 171 | 47 | 218 | |||
| Nº employees that returned to work in the reporting period after parental leave ended |
52 | 47 | 99 | 65 | 39 | 104 | |||
| Return to work rate | 95% | 100% | 97% | 97% | 100% | 98% | |||
| Total number of employees that returned to work after parental leave ended that were still employed 12 months after their return to work |
56 | 39 | 95 | 49 | 40 | 89 | |||
| Retention rate | 33% | 83% | 44% | 29% | 85% | 41% | |||
| Percentage of entitled employees that took family-related leaves 11 |
15% | 11% | 25% | NA | NA | NA |
| Miles de euros | 2024 | ||||
|---|---|---|---|---|---|
| Women | Men | Undeclared | Others | Total | |
| Spain | 559.9 | 699.4 | 0 | 0 | 1,259.3 |
| U.S. | 13,944.6 | 14,193.2 | 2,893.0 | 4.5 | 31,035.3 |
| Germany | 358.8 | 244.0 | 0 | 0 | 602.9 |
| RoW | 234.6 | 328.9 | 0 | 0 | 563.6 |
| Total | 15,097.9 | 15,465.6 | 2,893.0 | 4.5 | 33,461.0 |
| % | 45.1% | 46.2% | 8.6% | 0.0% | 100.0% |
| Miles de euros | 2023 | 2022 | ||||||
|---|---|---|---|---|---|---|---|---|
| Women | Men | Total | Women | Men | Total | |||
| Spain | 472.9 | 606.0 | 1,079.0 | 448.7 | 584.1 | 1,032.8 | ||
| U.S. | 14,502.9 | 15,627.6 | 30,130.5 | 15,406.4 | 15,652.4 | 31,058.8 | ||
| RoW | 516.5 | 436.8 | 953.2 | 384.4 | 412.2 | 796.6 | ||
| Total | 15,492.3 | 16,670.3 | 32,162.7 | 16,239.5 | 16,648.7 | 32,888.2 | ||
| % | 48.2% | 51.8% | 100.0% | 49.4% | 50.6% | 100.0% |
| Euros | 2024 | 202312 | |||||
|---|---|---|---|---|---|---|---|
| Women | Men | Total | Women | Men | Total | ||
| Germany | 1,789,625 | 2,892,919 | 4,682,544 | NAP | NAP | 4,920,204 | |
| RoW | 46,756 | 82,881 | 129,638 | 46,760 | 86,771 | 133,531 | |
| Total | 1,836,381 | 2,975,800 | 4,812,182 | 46,760 | 86,771 | 5,053,735 | |
| % | 38.2% | 61.8% | 100.0% | 0.9% | 1.7% | 100.0% |
100% of Biotest employees are entitled to take family leave.
Data is not broken down for Germany for reasons of confidentiality and personal data protection.
| ACCIDENT RATE | ||||||
|---|---|---|---|---|---|---|
| U.S. 2024 | U.S. 2023 | U.S. 2022 | ||||
| Women | Men | Women | Men | Women | Men | |
| Total number of work accidents with leave13 (LTI) without leave (NLTI) and first aid (FA) |
702 | 353 | 793 | 364 | 928 | 373 |
| Total number of work accidents with leave14 (LTI) | 51 | 26 | 48 | 30 | 76 | 19 |
| Hours worked | 13,950,784 | 9,536,219 | 14,720,459 | 9,973,427 | 19,160,137 | 11,166,314 |
| Accident Frequency Index15 | 3.7 | 2.7 | 3.3 | 3.0 | 4.0 | 1.7 |
| Severity Index16 | 0.05 | 0.03 | 0.07 | 0.07 | 0.11 | 0.09 |
| Number of fatalities as a result of work-related injuries and work-related ill health |
0 | 0 | 0 | 0 | NA | NA |
| Number of work accidents (contractors) | 0 | 1 | 2 | 3 | NA | NA |
| Number of days lost to work-related injuries and fatalities from workrelated accidents, work-related ill health and fatalities from ill health1717 |
719 | 241 | NA | NA | NA | NA |
| Number of cases of recordable work-related ill health | 0 | 0 | NA | NA | NA | NA |
| Spain 2024 | Spain 2023 | Spain 2022 | ||||
|---|---|---|---|---|---|---|
| Women | Men | Women | Men | Women | Men | |
| Total number of work accidents with leave13 (LTI) without leave (NLTI) and first aid (FA) |
105 | 118 | 108 | 116 | 90 | 122 |
| Total number of work accidents with leave14 (LTI) | 33 | 36 | 29 | 40 | 26 | 42 |
| Hours worked | 3,106,277 | 3,835,455 | 3,008,221 | 3,752,636 | 2,939,603 | 3,724,420 |
| Accident Frequency Index15 | 10.6 | 9.4 | 9.6 | 10.7 | 8.8 | 11.3 |
| Severity Index16 | 0.4 | 0.3 | 0.3 | 0.3 | 0.3 | 0.3 |
| Number of fatalities as a result of work-related injuries and work-related ill health |
0 | 0 | 0 | 0 | NA | NA |
| Number of work accidents (contractors) | 9 | 6 | 10 | 6 | NA | NA |
| Number of days lost to work-related injuries and fatalities from workrelated accidents, work-related ill health and fatalities from ill health1717 |
1,182 | 1,068 | NA | NA | NA | NA |
| Number of cases of recordable work-related ill health | 0 | 0 | NA | NA | NA | NA |
| Ireland 2024 | Ireland 2023 | Ireland 2022 | ||||
|---|---|---|---|---|---|---|
| Women | Men | Women | Men | Women | Men | |
| Total number of work accidents with leave13 (LTI) without leave (NLTI) and first aid (FA) |
14 | 12 | 11 | 9 | 7 | 3 |
| Total number of work accidents with leave14 (LTI) | 0 | 1 | 2 | 2 | 0 | 1 |
| Hours worked | 327,908 | 414,575 | 331,650 | 422,262 | 259,428 | 339,417 |
| Accident Frequency Index15 | 0 | 2.4 | 6.0 | 4.7 | 0 | 2.9 |
| Severity Index16 | 0 | 0.03 | 0.02 | 0.07 | 0 | 0 |
| Number of fatalities as a result of work-related injuries and work-related ill health |
0 | 0 | 0 | 0 | NA | NA |
| Number of work accidents (contractors) | 0 | 0 | 0 | 2 | NA | NA |
| Number of days lost to work-related injuries and fatalities from workrelated accidents, work-related ill health and fatalities from ill health1717 |
0 | 11 | NA | NA | NA | NA |
| Number of cases of recordable work-related ill health | 0 | 0 | NA | NA | NA | NA |
Total sum of accidents with sick leave (non itinere), accidents without sick leave and first aid cases.
Total number of accidents with sick leave (non itinere), excluding COVID.
Number of work accidents with sick leave (non itinere) excluding COVID / total number of actual hours worked * 10^6.
Number of workdays lost due to work accidents with sick leave excluding COVID (non itinere) / total number of actual hours worked *10^3 17. Lost days are calculated as the difference between the calendar days (without excluding holidays or vacation days) between the return-to-work date and the sick leave date.
| Germany 2024 | Germany 2023 | Germany 2022 | ||||
|---|---|---|---|---|---|---|
| Women | Men | Women | Men | Women | Men | |
| Total number of work accidents with leave13 (LTI) without leave (NLTI) and first aid (FA) |
80 | 20 | 41 | 17 | 63 | 13 |
| Total number of work accidents with leave14 (LTI) | 3 | 1 | 5 | 3 | 20 | 4 |
| Hours worked | 1,553,786 | 708,437 | 1,584,078 | 700,757 | 1,383,458 | 664,814 |
| Accident Frequency Index15 | 1.9 | 1.4 | 3.2 | 4.3 | 14.5 | 6.0 |
| Severity Index16 | 0.01 | 0.2 | 0.02 | 0.05 | 0.1 | 0.1 |
| Number of fatalities as a result of work-related injuries and work-related ill health |
0 | 0 | 0 | 0 | NA | NA |
| Number of work accidents (contractors) | 0 | 1 | 0 | 0 | NA | NA |
| Number of days lost to work-related injuries and fatalities from workrelated accidents, work-related ill health and fatalities from ill health1717 |
15 | 147 | NA | NA | NA | NA |
| Number of cases of recordable work-related ill health | 0 | 0 | NA | NA | NA | NA |
| Germany 2024 | Germany 2023 | Germany 2022 | ||||
|---|---|---|---|---|---|---|
| Women | Men | Women | Men | Women | Men | |
| Total number of work accidents with leave13 (LTI) without leave (NLTI) and first aid (FA) |
42 | 91 | 17 | 21 | 61 | 26 |
| Total number of work accidents with leave14 (LTI) | 12 | 32 | 14 | 18 | 9 | 23 |
| Hours worked | 1,385,493 | 1,702,268 | 1,608,089 | 2,029,541 | 1,451,784 | 1,792,284 |
| Accident Frequency Index15 | 8.7 | 18.8 | 8.7 | 8.9 | 6.2 | 12.8 |
| Severity Index16 | 0.08 | 0.3 | 0.23 | 0.18 | 0.26 | 0.05 |
| Number of fatalities as a result of work-related injuries and work-related ill health |
0 | 0 | 128.00 | 134.00 | NA | NA |
| Number of work accidents (contractors) | 2 | 2 | NA | NA | NA | NA |
| Number of days lost to work-related injuries and fatalities from workrelated accidents, work-related ill health and fatalities from ill health1717 |
110 | 478 | NA | NA | NA | NA |
| Number of cases of recordable work-related ill health | 0 | 0 | NA | NA | NA | NA |
| Professional category | Fixed Wage- Average 2024 | Fixed Wage- Average 2023 | Fixed Wage- Average 2022 | |
|---|---|---|---|---|
| Women | 215.5 | 234,199.4 | 287,311.2 | |
| Executives | Men | 358.8 | 294,979.5 | 283,288.9 |
| Women | 93.3 | 111,424.2 | 106,426.4 | |
| Directors | Men | 101.5 | 126,485.0 | 122,761.5 |
| Women | 65.1 | 80,243.2 | 77,615.6 | |
| Senior management Men |
69.0 | 85,223.4 | 82,403.3 | |
| Women Management Men |
44.1 | 57,197.7 | 56,150.6 | |
| 47.5 | 61,608.1 | 59,679.4 | ||
| Women | 32.8 | 44,306.0 | 42,881.6 | |
| Senior professionals | Men | 34.6 | 47,444.7 | 46,370.8 |
| Women | 30.1 | 38,582.9 | 37,776.2 | |
| Professionals | Men | 36.1 | 40,571.3 | 39,319.5 |
| Administrative staff / | Women | 28.4 | 28,917.7 | 28,202.0 |
| Manufacturing operators | Men | 31.0 | 29,434.8 | 28,774.1 |
Total sum of accidents with sick leave (non itinere), accidents without sick leave and first aid cases.
Total number of accidents with sick leave (non itinere), excluding COVID.
Number of work accidents with sick leave (non itinere) excluding COVID / total number of actual hours worked * 10^6.
Number of workdays lost due to work accidents with sick leave excluding COVID (non itinere) / total number of actual hours worked *10^3
Lost days are calculated as the difference between the calendar days (without excluding holidays or vacation days) between the return-to-work date and the sick leave date.
For reasons of confidentiality and personal data protection, remuneration data is not shown for professional categories with fewer than four individuals of each gender.
Grifols' 2024 data is presented in compliance with disclosure requirement S1-16 of the Corporate Sustainability Reporting Directive (CSRD), which mandates that information on the gender pay gap include the average gross hourly wage of all employees. For this reason, the average hourly remuneration includes supplementary or variable components. Data for 2023 and 2022 reflect the average gross annual remuneration, excluding supplementary or variable components.
| GRIFOLS |
|---|
| --------- |
| PLASMA CENTERS Professional category |
Fixed Wage- Average 2024 | Fixed Wage- Average 2023 | Fixed Wage- Average 2022 | |
|---|---|---|---|---|
| Executives | Women | NAP | NAP | 423,128.9 |
| Men | NAP | NAP | 327,646.3 | |
| Directors | Women | 122.0 | 228,290.9 | 200,068.6 |
| Men | 129.7 | 255,886.1 | 227,863.1 | |
| Senior management | Women | NAP | 159,492.0 | 158,824.1 |
| Men | NAP | 166,865.6 | 162,299.8 | |
| Management | Women | NAP | 112,733.3 | 105,920.4 |
| Men | NAP | 118,827.3 | 111,852.3 | |
| Women | NAP | 94,243.2 | 90,679.2 | |
| Senior professionals | Men | NAP | 96,902.6 | 93,429.4 |
| Women | 56.1 | 72,915.4 | 67,403.6 | |
| Professionals | Men | 60.3 | 75,593.9 | 70,289.3 |
| Administrative staff / Manufacturing operators |
Women | 28.7 | 43,135.0 | 42,367.8 |
| Men | 27.7 | 42,339.7 | 41,653.4 |
| REST OF ACTIVITIES | ||||
|---|---|---|---|---|
| Professional category | Fixed Wage- Average 2024 | Fixed Wage- Average 2023 | Fixed Wage- Average 2022 | |
| Executives | Women | 322.8 | 352,372.9 | 431,673.0 |
| Men | 440.8 | 438,137.8 | 402,767.9 | |
| Directors | Women | 182.8 | 233,132.0 | 222,949.8 |
| Men | 189.3 | 240,232.8 | 230,487.9 | |
| Senior management | Women | 129.5 | 179,262.4 | 170,195.2 |
| Men | 140.5 | 185,042.4 | 177,603.8 | |
| Management | Women | 94.5 | 139,678.2 | 133,476.6 |
| Men | 99.0 | 143,599.6 | 139,899.7 | |
| Senior professionals | Women | 81.9 | 116,940.4 | 112,693.1 |
| Men | 82.7 | 116,913.4 | 112,378.6 | |
| Professionals | Women | 54.5 | 82,492.1 | 80,065.1 |
| Men | 56.5 | 85,750.6 | 83,287.4 | |
| Administrative staff / | Women | 43.2 | 61,515.8 | 60,957.0 |
| Manufacturing operators | Men | 48.7 | 65,179.4 | 63,889.0 |
| Professional category | Fixed Wage- Average 2024 | Fixed Wage- Average 2023 | Fixed Wage- Average 2022 | |
|---|---|---|---|---|
| Executives | Women | NAP | NAP | NAP |
| Men | NAP | NAP | NAP | |
| Directors | Women | NAP | NAP | NAP |
| Men | ojo unidades de esta NAP columna de 2024!!!! |
NAP | NAP | |
| Senior management | Women | 74.5 - supongo que son |
128,321.6 | 110,980.0 |
| Men | miles,,, 64.1 |
120,028.7 | 119,091.7 | |
| Management | Women | 45.9 | 83,334.8 | 70,401.7 |
| Men | 48.8 | 88,575.4 | 80,401.0 | |
| Senior professionals | Women | 34.1 | 62,005.0 | 55,616.3 |
| Men | 38.0 | 66,819.6 | 59,794.8 | |
| Professionals | Women | 27.2 | 48,759.5 | 45,099.1 |
| Men | 32.6 | 51,747.3 | 48,099.6 | |
| Administrative staff / | Women | 23.9 | 39,247.8 | 37,382.6 |
| Manufacturing operators | Men | 25.2 | 38,461.4 | 36,875.3 |
| GRIFOLS | |
|---|---|
| --------- | -- |
| General | Environment | Social | Governance | Annexes |
|---|---|---|---|---|
| AVERAGE WAGE BY PROFESSIONAL CATEGORY AND GENDER / GERMANY - IN EUROS | ||||
|---|---|---|---|---|
| Professional category | Fixed Wage- Average 2024 | Fixed Wage- Average 2023 | Fixed Wage- Average 2022 | |
| Executives | Women | NAP | NAP | NAP |
| Men | NAP | NAP | NAP | |
| Directors | Women | 120.0 | 180,605.6 | 172,301.1 |
| Men | 135.0 | 188,398.1 | 183,879.9 | |
| Senior management | Women | 72.5 | 101,051.5 | 91,136.0 |
| Men | 73.7 | 109,449.3 | 116,751.0 | |
| Management | Women | 54.7 | 86,663.5 | 83,347.3 |
| Men | 59.1 | 91,333.4 | 88,562.4 | |
| Senior professionals | Women | 38.5 | 60,886.8 | 58,765.4 |
| Men | 42.6 | 64,367.0 | 60,060.9 | |
| Professionals | Women | 40.4 | 60,190.7 | 62,654.9 |
| Men | 38.3 | 60,853.1 | 60,651.4 | |
| Administrative staff / | Women | 23.4 | 35,622.2 | 34,632.7 |
| Manufacturing operators | Men | 22.9 | 34,675.7 | 33,317.0 |
| Professional category | Fixed Wage- Average 2024 | Fixed Wage- Average 2023 | |
|---|---|---|---|
| Executives | Women | 241,547.3 | NAP |
| Men | 326,014.3 | NAP | |
| Directors | Women | 177,946.2 | 151,593.6 |
| Men | 197,597.9 | 153,446.0 | |
| Senior management | Women | 141,440.8 | 112,625.6 |
| Men | 134,220.4 | 116,617.4 | |
| Management | Women | 109,797.4 | 100,860.7 |
| Men | 106,245.8 | 101,544.0 | |
| Senior professionals | Women | 81,310.1 | 76,169.4 |
| Men | 89,399.2 | 78,848.4 | |
| Professionals | Women | 65,764.9 | 58,187.4 |
| Men | 73,182.8 | 64,096.6 | |
| Administrative staff / | Women | 46,378.7 | 42,781.6 |
| Manufacturing operators | Men | 60,087.5 | 46,270.4 |
| Age | Fixed Wage- Average 2024 | Fixed Wage- Average 2023 | Fixed Wage- Average 2022 |
|---|---|---|---|
| <30 | 26.6 | 33,679.0 | 33,146.4 |
| 30-50 | 38.3 | 43,530.5 | 41,938.6 |
| >50 | 53.2 | 57,386.6 | 58,172.8 |
| AVERAGE WAGE BY AGE / U.S. - DATOS EN USD | ||||
|---|---|---|---|---|
| Age | Fixed Wage- Average 2024 | Fixed Wage- Average 2023 | Fixed Wage- Average 2022 | |
| <30 | 27.2 | 42,793.0 | 40,800.6 | |
| 30-50 | 49.5 | 67,408.5 | 62,434.9 | |
| >50 | 72.7 | 95,291.8 | 89,849.2 |
| AVERAGE WAGE BY AGE / IRELAND - IN EUROS | ||||
|---|---|---|---|---|
| Age | Fixed Wage- Average 2024 | Fixed Wage- Average 2023 | Fixed Wage- Average 2022 | |
| <30 | 28.8 | 50,611.4 | 48,304.7 | |
| 30-50 | 37.6 | 65,679.4 | 57,997.7 | |
| >50 | 36.4 | 63,748.0 | 82,253.7 |
| í | |
|---|---|
| AVERAGE WAGE BY AGE / GERMANY - IN EUROS | |||
|---|---|---|---|
| Age | Fixed Wage- Average 2024 | Fixed Wage- Average 2023 | Fixed Wage- Average 2022 |
| <30 | 23.2 | 38,261.8 | 36,957.2 |
| 30-50 | 31.5 | 46,699.2 | 44,162.1 |
| >50 | 39.2 | 56,358.5 | 53,524.1 |
| Age | Fixed Wage- Average 2024 | Fixed Wage- Average 2023 |
|---|---|---|
| <30 | 48,211.3 | 44,784.1 |
| 30-50 | 73,305.7 | 64,397.3 |
| >50 | 84,359.3 | 72,330.1 |
| Euros | 2024 | 2023 | 2022 | ||||||
|---|---|---|---|---|---|---|---|---|---|
| Women | Men | Total | Women | Men | Total | Women | Men | Total | |
| Total average salary | 315,847.7 | 404,745.5 | 371,206.0 | 245,745.4 | 301,275.3 | 281,113.3 | 250,329.3 | 292,935.3 | 277,054.2 |
| Executives, employees and Board Members |
186 | 307 | 493 | 179 | 314 | 493 | 186 | 313 | 499 |
| Salary gap | 21.96% | 18.43% | 14.50% |
| Adjusted Gender Pay Gap 2024 |
Gender Pay Gap 2024 |
Adjusted Gender Pay Gap 2023 |
Gender Pay Gap 2023 |
Adjusted Gender Pay Gap 2022 |
Gender Pay Gap 2022 |
|
|---|---|---|---|---|---|---|
| Executives | NAP | 39.95% | NAP | 20.60% | NAP | -1.40% |
| Directors | 0.32% | 8.10% | 9.97% | 11.91% | 6.50% | 13.30% |
| Senior management | 4.21% | 5.65% | 5.84% | 5.84% | 5.30% | 5.80% |
| Management | 6.06% | 7.08% | 5.47% | 7.16% | 4.40% | 5.90% |
| Senior professionals | 1.81% | 5.10% | 3.23% | 6.62% | 4.00% | 7.50% |
| Professionals | 9.54% | 16.63% | 2.15% | 4.90% | 3.00% | 3.90% |
| Administrative staff / Manufacturing operators |
1.27% | 8.35% | 0.79% | 1.76% | 0.90% | 2.00% |
| Adjusted Gender Pay Gap 2024 |
Gender Pay Gap 2024 |
Adjusted Gender Pay Gap 2023 |
Gender Pay Gap 2023 |
Adjusted Gender Pay Gap 2022 |
Gender Pay Gap 2022 |
|
|---|---|---|---|---|---|---|
| Executives | NAP | NAP | NAP | NAP | NAP | -29.10% |
| Directors | NAP | 5.92% | NAP | 10.78% | 2.80% | 12.20% |
| Senior management | NAP | NAP | NAP | 4.42% | NAP | 2.10% |
| Management | NAP | NAP | 3.46% | 5.13% | 1.80% | 5.30% |
| Senior professionals | NAP | NAP | 0.82% | 2.74% | -0.60% | 2.90% |
| Professionals | 5.58% | 6.92% | 2.40% | 3.54% | 3.70% | 4.10% |
| Administrative staff / Manufacturing operators |
-2.61% | -3.44% | -1.87% | -1.88% | -2.50% | -1.70% |
Due to confidentiality and personal data protection, gender pay gap data is not shown for professional categories with fewer than four individuals of each gender.
The adjusted gender pay gap data is not shown for categories where it is not possible to obtain a statistically significant result through the econometric model.
Grifols' 2024 data is presented in compliance with disclosure requirement S1-16 of the Corporate Sustainability Reporting Directive (CSRD), which mandates that information on the gender pay gap include the average gross hourly wage of all employees. For this reason, the average hourly remuneration includes supplementary or variable components. Data for 2023 and 2022 reflect the average gross annual remuneration, excluding supplementary or variable components.
| GRIFOLS |
|---|
| --------- |

| GENDER PAY GAP / U.S. - REST OF ACTIVITIES | |||||||
|---|---|---|---|---|---|---|---|
| Adjusted Gender Pay Gap 2024 |
Gender Pay Gap 2024 |
Adjusted Gender Pay Gap 2023 |
Gender Pay Gap 2023 |
Adjusted Gender Pay Gap 2022 |
Gender Pay Gap 2022 |
||
| Executives | NAP | 26.77% | NAP | 19.57% | NAP | -7.20% | |
| Directors | 0.77% | 3.41% | 1.25% | 2.96% | 1.30% | 3.30% | |
| Senior management | 8.54% | 7.88% | 1.20% | 3.12% | 2.50% | 4.20% | |
| Management | 2.68% | 4.56% | 5.46% | 2.73% | 6.70% | 4.60% | |
| Senior professionals | 1.66% | 0.98% | 2.76% | -0.02% | 1.30% | -0.30% | |
| Professionals | 2.54% | 3.44% | 1.72% | 3.80% | 2.30% | 3.90% | |
| Administrative staff / Manufacturing | 6.38% | 11.26% | 4.82% | 5.62% | 4.50% | 4.60% | |
| operators |
| Adjusted Gender Pay Gap 2024 |
Gender Pay Gap 2024 |
Adjusted Gender Pay Gap 2023 |
Gender Pay Gap 2023 |
Adjusted Gender Pay Gap 2022 |
Gender Pay Gap 2022 |
|
|---|---|---|---|---|---|---|
| Executives | NAP | NAP | NAP | NAP | NAP | NAP |
| Directors | NAP | NAP | NAP | NAP | NAP | NAP |
| Senior management | NAP | -16.18% | NAP | -6.91% | NAP | 6.80% |
| Management | NAP | 5.93% | NAP | 5.92% | NAP | 12.40% |
| Senior professionals | 5.30% | 10.40% | 7.08% | 7.21% | 4.90% | 7.00% |
| Professionals | 10.31% | 16.52% | 1.63% | 5.77% | NAP | 6.20% |
| Administrative staff / Manufacturing operators |
3.82% | 5.04% | 0.37% | -2.04% | -1.00% | -1.40% |
| Adjusted Gender Pay Gap 2024 |
Gender Pay Gap 2024 |
Adjusted Gender Pay Gap 2023 |
Gender Pay Gap 2023 |
Adjusted Gender Pay Gap 2022 |
Gender Pay Gap 2022 |
|
|---|---|---|---|---|---|---|
| Executives | NAP | NAP | NAP | NAP | NAP | NAP |
| Directors | NAP | 11.09% | NAP | 4.14% | NAP | 6.30% |
| Senior management | NAP | 1.63% | NAP | 7.67% | NAP | 21.90% |
| Management | NAP | 7.39% | NAP | 5.11% | NAP | 5.90% |
| Senior professionals | 9.46% | 9.56% | 2.37% | 5.41% | NAP | 2.20% |
| Professionals | 4.21% | -5.56% | 4.09% | 1.09% | 2.10% | -3.30% |
| Administrative staff / Manufacturing operators |
0.35% | -2.03% | 0.13% | -2.73% | -1.40% | -3.90% |
| Adjusted Gender | Gender Pay Gap | Adjusted Gender | Gender Pay Gap | |
|---|---|---|---|---|
| Pay Gap 2024 | 2024 | Pay Gap 2023 | 2023 | |
| Executives | NAP | NAP | NAP | NAP |
| Directors | NAP | 10.09% | NAP | 1.21% |
| Senior management | NAP | 1.15% | NAP | 3.42% |
| Management | -3.68% | -2.92% | -0.83% | 0.67% |
| Senior professionals | 1.17% | 4.70% | 3.14% | 3.40% |
| Professionals | 2.63% | 10.38% | 1.93% | 9.22% |
| Administrative staff / Manufacturing operators |
-0.30% | 21.51% | -6.67% | 7.54% |
Respect for the rights and dignity of every individual is a core principle of Grifols' activity. The company works to protect human rights in all of its actions, while promoting and safeguarding the well-being of the communities where it operates.
This pledge includes defending the rights of employees across its value chain. Grifols is also dedicated to continuous improvement and works actively to mitigate both real and potential risks and impacts across its operations and value chain. As part of these efforts, the company strives to meet the reporting requirements defined by the Corporate Sustainability Reporting Directive (CSRD) in the coming years.
| S2 WORKERS IN THE VALUE CHAIN |
|||||
|---|---|---|---|---|---|
| Material IROs | Type | Description | |||
| LABOR CONDITIONS | |||||
| Generation of quality employment | + SP |
Grifols promotes social progress by generating high-quality direct and indirect employment through its operations and across its value chain. The company is committed to maintaining open lines of communication to minimize potential impacts on workers across its value chain. |
|||
| Workplace accidents and occupational diseases |
- SP |
An inadequate work environment can lead to an increase in accidents. To mitigate this risk, Grifols expects its suppliers to comply with a series of occupational health and safety requirements. |
|||
| EQUAL TREATMENT AND OPPORTUNITIES FOR ALL | |||||
| Discrimination and workplace harassment in our value chain |
- SP |
Grifols rejects all forms of discrimination, harassment and all practices that promote inequality, and actively works to build a fairer and more equitable society. |
|||
| OTHER LABOR RIGHTS | |||||
| Labor rights violations in the value chain |
- SP |
Grifols is committed to protecting human rights and works actively to eradicate modern slavery, forced or compulsory labor, and child labor throughout its value chain. The company takes proactive steps to mitigate any potential related impacts. |
|||
The following policies, actions, metrics and targets enable Grifols to efficiently manage the key impacts, risks and opportunities related to employees across its value chain.
| Material Sub-topics | Policies | Actions | Metrics and Targets (S2-5) |
|---|---|---|---|
| Working conditions | • Code of Conduct • Human Rights Policy |
• Continuous improvement in identifying and managing impacts and risks in the value |
Implement ESG criteria among suppliers up to 60-80% of total volume of expenditure. |
| Equal treatment and opportunities for all |
• Diversity and Inclusion Policy • Security and Safety Policy • Procurement Policy |
chain. | |
| Other work-related rights |
• Supplier Code of Conduct • Grifols Ethics Line Policy |
More information on advances in 2024 and next steps: "Management of relationships with suppliers-Governance." More information on the latest progress: "Agenda Grifols 2030-General Information."
Grifols is committed to conducting its global activities with respect for human rights, compliance with applicable laws and the adoption of fair labor practices. The company developed a global strategy to promote and ensure responsibility and commitment to human rights across all its operations, using internationally recognized frameworks as a foundation (UN Global Compact, UN Guiding Principles on Business and Human Rights, OECD Guidelines for Multinational Enterprises, and the ILO Declaration on Multinational Enterprises).
The company's commitment to upholding fundamental human rights is embedded into its corporate strategy and reflected in various codes and policies that underpin its corporate culture. These include the Code of Conduct, Human Rights Policy, Diversity and Inclusion Policy, Occupational Health and Safety Policy, Procurement Policy, Supplier Code of Conduct and the Grifols Ethics Line Policy, among others.
Grifols recognizes the crucial role of stakeholders in its success, particularly workers who form part of its value chain.
Grifols maintains close relationships with employees working across its value chain at its various facilities, engaging in direct and frequent dialogue to ensure effective communication. That said, it has limited control over the external workforce not directly supervised by its teams. To this end, the company makes concerted efforts to enhance both direct and indirect collaboration with workers across its value chain, recognizing that fluid communication helps prevent conflicts, fosters a safe and respectful environment, boosts engagement, and enables the early identification of human rights-related risks and concerns.
Grifols also operates the Grifols Ethics Line, an independent and accessible communications channel for employees in its value chain and all its stakeholders to confidentially report any concerns or needs.
In 2024, Grifols received 0 reports of human rights violations related to its upstream and downstream value chain workers.
More information on these policies and how they address the impacts on human and labor rights: "Our People-Social."
More information on business practices with sales partners: "Management of relationships with suppliers-Governance."
More information on Grifols' supplier relations and workforce: "Stakeholders-General Information" and "Management of relationships with suppliers-Governance."
More information on the ethics Line: "Grifols Ethics Line-Governance."

Grifols has been analyzing and reviewing its human rights due diligence processes since 2022 to progressively identify and manage human rights risks and impacts across its value chain, covering 100% of its own operations, Tier 1 suppliers, joint ventures and others.
In general, Grifols has control measures in place to mitigate the main risks and their derived impacts in terms of human rights, which translates into a low residual risk globally for most of Grifols' activities.
Grifols' Supplier Code of Conduct and Global Procurement Policy serve as effective tools in helping the company mitigate and respond optimally to potential risks and impacts, ensuring the well-being of its employees and suppliers. Building on these initiatives, Grifols is actively improving its formal plans and controls to ensure respect for human rights throughout its value chain.
In parallel, the Global Procurement team remains focused on aligning supplier relations procedures with the industry's latest regulatory developments. The company is working actively to roll out the necessary mechanisms to improve its supplier evaluation and due diligence processes.
Grifols' plasma donors and the communities in which its donation centers operate are the primary stakeholders impacted by Grifols's activities. Plasma-derived medicines are only possible through the generosity of donors.
The company extends its commitment and social reach to all the communities in which it operates with initiatives that contribute to local development and/or are related to human rights in areas such as health, education, and the environment. These social initiatives amplify Grifols' positive impact on other groups, including disadvantaged individuals and social groups.
Grifols takes pride in its donors and being a strong community partner through its activities directly and through its foundations: J.A. Grifols Foundation, Fundació Probitas and Fundació Víctor Grífols i Lucas.
| S3 AFFECTED COMMUNITIES |
||
|---|---|---|
| Material IROs | Type | Description |
| COMMUNITIES' ECONOMIC, SOCIAL AND CULTURAL RIGHTS | ||
| Health and well-being of plasma donors and their communities |
+ - OO SP R |
Ensuring the health and well-being of plasma donors is among Grifols' topmost priorities. Donating plasma is a safe and highly regulated process conducted in meticulously controlled centers and highly-trained staff. As an industry leader, the company goes above and beyond compliance by implementing best practices that benefit both donors and local communities. |
| Contribution to the local and social development of communities |
+ OO SP |
With 399 plasma donation centers and 15 manufacturing complexes, Grifols promotes the local and social development of areas where its centers and plants are located, generating value for both donors and communities. |
+ Positive impact - Negative impact R Risk OO Own Operation SP Supply Chain
The following policies, actions, metrics and targets allow for efficient management of the main IROs related to donors and the communities in which Grifols operates.
| Material Sub-topics | Policies | Actions | Metrics and Targets |
|---|---|---|---|
| Communities' economic, social and cultural rights |
• Plasma Donor Policy • Corporate Donor Safety Policy • Social Action Policy and Community Investment Policy • Human Rights Policy • Grifols Ethics Line Policy |
• Grifols' health questionnaires for assessing donor eligibility include the most recent FDA Individual Risk Assessment Guidance, although many of the company's current standards are even more stringent. • Grifols directly supports the research initiatives of diverse scientific institutions and associations focused on assessing the potential effects of plasmapheresis on donor health. |
• Achieve 90% approval among donors for positive customer service (good or excellent rating) • Attain 80% referral rate from active donors • Increase ratings via the Donor Hub by 45% • Increase the number of initiatives and social investment by 50% • Allocate 25% of social initiatives to STEM activities for women • Increase annual funding to the J.A. Grifols Foundation by 10% • Increase Víctor Grífols i Lucas Foundation resources for bioethics scholarships by 10% and activities by 20% |
Grifols fosters active communication with its donors to maintain an open and close relationship, enabling the company to understand their concerns and needs. The company provides donors with useful information to educate on the process before, during and after donation. In addition, it works with local communities to raise awareness of the importance of plasma donation to produce plasma-derived medicines for patients who need them. Grifols core channels and actions include:
Respect for dignity and human rights is intrinsic to all of Grifols' activities. The company supports the basic principles of the Universal Declaration of Human Rights (1948), the Declaration of Helsinki (1964) and the UNESCO Universal Declaration on Bioethics and Human Rights (2005). Grifols Code of Conduct, which governs the company's interactions with all stakeholder groups including donors, are grounded on respect for human rights. This principle is explicitly outlined in Grifols' Donor Policy, which also reaffirms its commitment to comply with the legal regulations governing plasma donations in each country, as well as to uphold non-discrimination and the protection of donor health and safety.
Grifols is a trusted source of clear information for donors at every stage of the donation process. A signed informed consent prior to donation is a fundamental aspect in providing important donor information.

donors
Potential donors must undergo a rigorous screening and selection process that begins with a physical examination.
The donor's medical information is recorded in their file and handled confidentially in compliance with Grifols' Global Privacy and Data Protection Policy. Prior to each donation, a trained Grifols staff member checks donors' vital signs, weight, hematocrit and plasma-protein levels to confirm they are able to safely donate. These routine screenings and physical examinations reflect Grifols' unwavering commitment to promoting and protecting donor health.
On the day of donation, if medical evaluations reveal any abnormal levels or irregular parameters that could indicate an underlying health issue, donors might be deferred until they see their physician or levels return to a normal range. These parameters include: irregular heart rate, elevated body temperature, high or low hematocrit, high or low total protein, and lipemic plasma.

receive in plasma donation centers are also drivers of frequent donations.
*According to Grifols survey conducted in 2023 on 1,300 donors.

Safety in the donation process is paramount to ensuring the health and wellbeing of plasma donors, who are a priority for Grifols. The company upholds the highest safety standards in its centers and works to continue leading the industry in the implementation of best practices.
Donating plasma is considered a safe procedure, as it is highly regulated and carried out in specialized centers that undergo rigorous controls. Additionally, the qualification criteria for donors are strict and a plasmavigilance system tracks potential adverse effects in donors to help ensure their health and safety at all times.
Plasma can be procured from whole blood donations (recovered plasma) or via plasmapheresis (sourced plasma), a specific plasma-donation technique developed by Josep Antoni Grifols i Lucas.
Plasma collection for the production of plasma-derived medicines is subject to strict regulations by global healthcare authorities and Good Manufacturing Practices (GMPs). The U.S. Food and Drug Administration (FDA) is the highest health authority in the United States, while the European Medical Agency (EMA) oversees this function in Europe. Grifols donations centers also comply with the voluntary IQPP (International Quality Plasma Program) certification from the Plasma Protein Therapeutics Association (PPTA), which sets and monitors additional quality standards.
Donating plasma is considered a highly safe procedure, with few or no side effects. Plasmapheresis removes plasma and returns red blood cells, platelets and other components to the donor. The body regenerates donated plasma in roughly 48 hours, compared to the two months it takes to regenerate red blood cells procured from whole blood donations.
In 2024, Europe adopted a new directive to guarantee the safety and quality of substances of human origin (SoHO), including plasma donations. The objective of this new regulation is to improve access to SoHO therapies, which denotes a critical issue in the healthcare systems of all EU member states.
Grifols plasma donation centers follow the highest standards of quality and safety that are routinely monitored to ensure donor safety and the quality of the donated plasma. In 2024, Grifols did not receive any administrative actions at its plasma donation centers related to the suspension, renewal or loss of any license or certification, nor any warning letters or suspension of any regulated activity.
| 2024 | 2023 | 2022 |
|---|---|---|
| 112 | 137 | 119 |
| 84 | 196 | 182 |
| 129 | 169 | 108 |
| 148 | 97 | 123 |
| 473 | 599 | 532 |
Includes Biotest.
* More than 90% of FDA inspections have been closed with 0 observations.
Grifols has a procedure in place that outlines how to manage and categorize donor adverse events (DAEs) according to the definitions set by the PPTA IQPP standard.
The procedure is activated when a donation-center professional observes that a donor is experiencing an adverse event in any of the following situations: upon the donor's arrival at the center prior to donation; during the screening process; during the donation process; after plasma donation or after leaving the facility; during or after donor immunization; and if reported on the day of donation or on a different date. Adverse events are documented as soon as possible after their occurrence or report, and immunization reactions are registered in the appropriate record. Only trained and certified personnel can manage and document DAEs.
Immediately following an adverse event, donors must receive appropriate treatment and the DAE is documented in their file. Grifols Quality Department thoroughly reviews all DAEs to ensure their proper management and classification before closing the case. The final step is completion of the Donor Adverse Events Electronic Report (DAER), which promotes plasma-donation safety and quality by guaranteeing DAEs are correctly managed.

DAEs include bruising, hypertension, citrate reactions, allergic reactions, hyperventilation, hemolysis, cardiovascular or respiratory events, immunization and aeroembolism.
In addition, this procedure allows Grifols to collect, analyze, monitor and evaluate trends in donor adverse events across its network of centers. Another testament to its commitment to continuous improvement and contributing to the health and safety of donors. At the same time, it facilitates the evaluation of donor characteristics or attributes to establish viable intervention strategies based on potential changes in donor demographics, eligibility criteria, plasmapheresis-related technology, regulatory changes and other factors.
In line with previous years, Grifols' U.S. plasmavigilance data in 2023* revealed minimal side effects or donor adverse events (DAE)* among its donors: only 0.26% reported any adverse effects as a result of the donation process. Most were mild, with a predominance of hypotension and hematomas. Reactions requiring medical assistance were extremely rare (0.0075% of Grifols' total donations). *Plasma surveillance data in 2023 according to DAE categorizations established by the PPTA
Adverse event data continue to confirm the safety of plasma donation.

(Plasma Protein Therapeutics Association) IQPP Standard for the recording of donor adverse events.
Data published with a one-year delay in adherence to required reporting cycles.

In 2024, Grifols' updated its health questionnaire for assessing donor eligibility to align with the FDA's Individual Risk Assessment Guidance. In many cases, Grifols' criteria are more stringent than FDA guidance
As part of its commitment to donor health and safety, Grifols supports research on the potential effects of plasmapheresis on donors' health, both directly and via collaborations with scientific organizations. To date, various studies have shown that frequent plasma donation should not negatively affect donor health nor cause serious adverse effects. Studies have also found that plasmapheresis can reduce cholesterol levels and may even have a beneficial effect on donors with increased blood pressure.
Published in 2023 in the scientific journal Transfusion, this transversal PPTA study sought to determine if plasma donation at FDA-defined frequency and volume levels affected donor health. Donors from 14 U.S. plasma donation centers, including several Grifols plasma donation centers, took part in the study, which concluded that paid plasma donations at these levels are consistent with donor health and well-being. Even at the highest frequency, plasmapheresis alone was found to produce no negative health effects.
Study: Effects of donation frequency on U,S, source plasma donor health
More than 1.1 million donors, who collectively account for 72% of the U.S. source plasma collected over a four-month period, participated in the first industry-wide, multi-company study on the incidence, frequency and type of adverse effects of plasmapheresis. Promoted by the PPTA in cooperation with several industry firms, the study confirmed the overall safety of plasmapheresis. Following FDA standards of collection volumes and donation frequency, the rate of adverse events (AE) was 1.58 per 10,000 donations. Moreover, 90% of AEs were minor, such as hypotension and phlebotomyrelated hematomas, with no reports of serious or severe adverse events. The study's findings were published in 2021 in Transfusion.
Study: Plasmavigilance: Source plasma joins the call to arms
Unlike whole blood donations, this study found no loss of iron or decline in ferritin levels as a result of regular plasma donations. These findings deem it unnecessary to monitor donors' iron levels or recommend iron supplements.
Study: Frequent source Plasma donors are not at risk of iron depletion: The Ferretin Levels in Plasma Donor (FLIPD)

Apheresis or low-density lipoprotein extraction is used to treat patients with familial hypercholesterolemia. Low-volume plasmapheresis used for plasma donations can similarly reduce cholesterol levels in some donors.
This study was designed to evaluate the effect of plasmapheresis on total LDL and HDL cholesterol levels in a population of healthy donors. The results suggest that, in donors with elevated baseline cholesterol levels, total and LDL cholesterol levels may decrease with frequent plasma donation. For donors with low HDL levels, the study suggests that levels may increase.
Study: Prospective multicentre study of the effect of voluntary plasmapheresis on plasma cholesterol levels in donors
Grifols led a study to discern the potential effects of plasmapheresis on blood pressure, finding a beneficial effect among donors with high baseline blood-pressure levels, whose systolic and diastolic blood pressure dropped significantly when their donation intervals were under 14 days. No decline in blood pressure was observed among donors with normal baseline blood pressure levels.
Study: The effect of plasmapheresis on blood pressure in voluntary Plasma donors,
In 2023, Transfusion published the results of a study to discern the motivating factors of donors' decision to stop donating plasma. The survey was conducted among donors in 14 plasma donation centers of several companies, Grifols included, who had stopped donating for at least six months. The most common reasons cited were lack of time (30.2%), insufficient compensation (14.7%) and procrastination (14.3%), showing that real or perceived negative health impacts were generally not the main drivers behind their decision to stop donating.
Study: Why do US source Plasma donors stop donating?
Grifols' U.S. donation centers are located throughout the country, with no concentration in a specific geographic region.
When evaluating suitable plasma donation center sites, Grifols considers the strength of the area's chambers of commerce and the opportunities it offers to engage with local organizations and governments. For Grifols, a community's active participation in the plasma donation process is critical to encouraging plasma donation and ensuring life-sustaining plasma-derived treatments for patients who need them.
In 2024, Grifols plasma-donation network comprised 298 plasma centers in the U.S., 98 in Europe and 3 in the rest of the world, all located in communities with a strong commitment to social progress.
Grifols' plasma-center employees actively participate in donor communities and promote initiatives aimed at engaging and forging ties with local residents. These activities include educational, social and awareness events to highlight the importance of plasma donation for people who rely on plasma-derived medicines. Plasma donation centers also collaborate with local businesses and non-governmental organizations to raise awareness on the vital role of plasma and the production of plasma-derived medicines.
The company considers other criteria when choosing communities for its plasma donation centers, including a strong employment pool, low viral markers, below-average crime statistics and community heterogeneity, which is critical to ensuring a diverse donor pool.
In addition, new plasma donation centers are designed to reduce their environmental impact and optimize energy use to promote an ecological and efficient environment for donors and employees. To this end, they use low environmental impact materials with sustainability certifications and energyefficient LED lighting.

Plasma donation centers are engines of local development. Grifols strives to maximize its positive impact and create opportunities within the communities where it operates. To this end, it organizes communityoutreach events, donation drives and volunteer activities, both directly and through the J.A. Grifols Foundation.


Grifols has collaborated with Habitat for Humanity since 2014 to help provide safe, decent and healthy housing in communities across the country. In 2024, Grifols supported initiatives in San Diego, Los Angeles and Emeryville, California; and Raleigh and Clayton, North Carolina.
Support in 2024 130 volunteers 65 people or 16 families benefited +825 hours USD 200,000

Grifols partners with United Service Organizations (USO), a national nonprofit that works to keep U.S. military service members connected to their
home environments during their service. The partnership helps build ties between Grifols employees and local USO affiliates.
Support in 2024 +25 volunteers +100 hours USD 200,000
Grifols employees and plasma donors participate in food drives and fundraising campaigns for local food banks such as "Box Out Hunger" intitative.
200,000 meals 2.7M million meals in 4 years +1,808 hours
No. of local organizations supported in
2024
19
General Environment Social Governance Annexes
2024
EUR
Grifols also engages in social-outreach actions through the J.A. Grifols
Foundation that promotes activities that benefit both plasma donors and their communities.
The J.A. Grifols Foundation was created in 2008 in honor of Dr. José Antonio Grifols, a pioneer in the development of the plasmapheresis technique. The Foundation leads an array of initiatives to enhance the health and well-being of plasma donors and their communities, including projects to raise awareness on the importance of plasma, recognize donors for their generosity and drive progress in local communities.
These initiatives have a positive impact on both the donors and their communities. The Foundation's activities are currently centered in the United States.
The Foundation's board of directors includes patient, plasma donor and employee representatives, who meet regularly to approve activities and community-enhancement grants. In 2024, the board approved 19 grants totaling more than EUR 452,000 to local organizations focused on delivering civic, social or educational programs for young people and at-risk populations.
Its scope of action also encompasses an emergency assistance program for plasma donors. The program began as a pilot program with two centers in 2023 and expanded to six centers in 2024. It provides a grant to the National Organization for Rare Disorders (NORD) that manages the program on behalf of the Foundation.
Donation center employees also promote Foundation initiatives through their volunteer work with the grantee organizations.




Since 2020, Grifols has analyzed and measured the value created by its U.S. and European plasma donation centers using the Social Return on Investment (SROI) methodology. The value created includes that generated for donors and for local communities.
The value created by Grifols for its donors and communities in 2024 has decreased slightly compared to 2023, when the value provided to donors was \$2,579 million and the impact on local communities reached \$2,478 million. This reduction is mainly due to a decrease in the number of donors. For more information, see the Sustainable Growth section of this report. Additionally, donor compensation has also stabilized, explaining the variations in the impact created on local communities.
| Impact on donors | |
|---|---|
| USD 2,323 M |
Impact on local communities
USD 2,252 M
Grifols' social commitment and outreach extend to all of its communities of operation with initiatives aimed at fostering local development in the areas of health, education and the environment. These social initiatives amplify Grifols' positive impact on disadvantaged individuals and marginalized groups.
The principles and guidelines in Grifols' Sustainability Policy inform its Corporate Social Action and Community Investment Policy, both of which fall under the umbrella of its Sustainability Master Plan.
The company's social action supports the United Nations 2030 Agenda for Sustainable Development by investing in initiatives that advance shared values and sustainable development. Social-impact initiatives are carried out directly and through Grifols foundations.
All social-impact investment and donation decisions are governed by Grifols Code of Conduct. Social Impact Committees established at Grifols sites follow a standard operating procedure (SOP) to ensure transparency and alignment of all activities with Grifols' mission and Social Action and Community Investment Policy.
Among its provisions, this SOP outlines the procedures for receiving and processing grant and/or donation applications across North America, Australia, the United Kingdom and the European Union (EU).
Additionally, Grifols coordinates initiatives and projects through the Probitas Foundation to increase access to medical treatment for vulnerable populations. The company also supports the Víctor Grifols i Lucas Foundation, established to promote bioethics as an engine for social and scientific progress. The foundation's efforts guide and support society in ensuring that technological advancements do not undermine ethics or fundamental rights, particularly in the realm of biomedicine.

*Not including foundations
More information on the Probitas Foundation and the Víctor Grifols i Lucas Foundation: see specific sections.
We aspire to improve access to medical care and encourage healthy lifestyle habits, including food security and sports.

*Breakdown of subsidized initiatives, excluding donation-center activities.
We promote science and educational equality among young people by offering grants, sponsorships and scholarships.

We work to improve the environment by promoting local park development programs and initiatives to raise awareness on environmental issues.

Grifols supports initiatives aimed at enhancing people's health and well-being, including food security and sports.


Grifols supports food banks in the U.S. and Germany, which provide food and basic necessities for thousands of people across both countries.
Support in 2024 USD 28,000

This non-profit promotes sustainable and healthy nutrition for children through practical educational programs.
Support in 2024 USD 27,765
150 beneficiaries

Based in Sydney, this foundation focuses on treating and preventing blindness and other vision problems in individuals and communities, especially among Aboriginal and Torres Strait Australians.
720 beneficiaries
Grifols supports children by collaborating with over 40 local organizations globally to collect toys around the holidays. In 2024, the company collected and donated more than 7,000 toys worth close to USD 100,000.
Grifols promotes science and STEM skills among women and minority groups as core educational priorities.



U.S.
Grifols promotes STEM learning among women, African Americans, indigenous people and at-risk youth through scholarships and other initiatives.
Support in 2024 USD +100,000 +99,000 beneficiaries

Grifols finances two nursing scholarships and the Saturday Science Academy program at CDU to address healthcare inequalities and encourage disadvantaged and ethnically diverse youth in South Los Angeles to pursue careers in healthcare.
Support in 2024 USD 50,000 +300 beneficiaries

Fulbright grants are offered to recent college graduates interested in earning doctoral or master's degrees at U.S. universities. Grifols has collaborated with the prestigious Fulbright program since 2013.
Grifols supports education by collaborating on school-supply campaigns with schools in the United States and Germany. In 2024, the company donated more than USD 90,000 worth of school supplies to 93 schools.
Grifols aspires to raise awareness on environmental issues, including the efforts to fight climate change and protect natural areas and their biodiversity.


Grifols supports programs to promote greener and more sustainable environments in urban areas, encourage eco-friendly habits among young people, lead community clean-ups and prevent pollution. Through these initiatives, the company helps improve people's quality of life, preserve the environment and raise environmental awareness.

TLC works to protect water systems, natural habitats and farmland in the Clayton, North Carolina area. In parallel, it works to connect people with nature through land stewardship and community action, and supports the NextGen Farming initiative, supporting start-up farmers via educational opportunities and other resources.
In Spain, Grifols collaborates with several projects in its communities of operation to promote its values and social impact. The company provides funding for different entities in sports, cultural, educational, social and environmental ambits for a maximum two-year period. An evaluation committee selects beneficiary projects following the criteria set forth in a standard operating procedure. Projects supported in 2024 include:
Fundación Rivus, which works to improve and preserve river systems, especially in the Besòs and Tordera River basins located near the Parets
Initiatives supported in 2024: 11 initiatives Total investments: EUR 158,014 Employees participation, including their families: 59 people
del Vallès facilities. In this regard, Grifols sponsored the "Discover the River" drawing contest and the "Sergi Mingote Academic Award" to engage young people in the study and importance of these river basins and their surrounding areas.
Cotillas CD Women's Soccer Team: The company also sponsors the Cotillas CD soccer team in Las Torres de Cotillas (Murcia), which is also home to one of its production plants. For Grifols, sports are one of the most powerful levers for advancing gender equality.

of physical, mental and social well-being. As a mission-driven organization, Probitas runs social and healthcare programs in Spain that specifically target children, adolescents and
families who are in vulnerable situations or at risk of social exclusion.
Internationally, it works to improve the living conditions and healthcare access of communities in remote and resource-poor areas. Through these efforts, Probitas strengthens public health systems in these regions.
At the same time, the Foundation actively supports research and collaborates with universities and research centers to study the impact of its programs.
Probitas works with various social and healthcare entities through a partnership model, co-designing projects to ensure they are impactful, sustainable and replicable.
The Probitas Foundation contributes to the social sustainability of Grifols S.A., which allocates 0.7% of its annual profits to support the Foundation's initiatives.
The Probitas Foundation's health and social action programs in Spain focus on promoting the holistic development of children and adolescents in vulnerable situations.
These programs support health education, socio-educational assistance, the coverage of basic needs such as food, and the professional development of people who work with minors. Probitas projects are developed collaboratively with various stakeholder group, including social organizations, schools, public administrations and families.
In 2024, the Foundation led more than 295 initiatives under its three main programs: Health Education, Specialized Health and Research, and Training and Development.
More than 10,000 children in 58 municipalities participated in these programs in the 2023-24 academic year. In addition, 57 Grifols employees participated in the "Donate Your Christmas Basket" campaign by donating their holiday gift boxes, either partially or in full. These contributions reflected a total value of EUR 4,800.
This program targets populations living in remote regions of the world with limited healthcare resources. In these areas, diseases represent a major public health issue, causing immense human suffering, stigmatization and high rates of morbidity and mortality.
Probitas promotes health equity with programs dedicated to addressing Neglected Tropical Diseases (NTDs) and rehabilitating laboratories in order to improve diagnosis, prevention and community health.
Probitas projects are developed in collaboration with local entities and health authorities in each country, within the context of primary healthcare. Community involvement is encouraged to ensure that healthcare is prioritized, with healthcare personnel trained to support these efforts.
In 2024, Probitas rehabilitated and equipped four new clinical diagnostic laboratories, developed five NTD projects and led three professional scholarship projects.


Awards granted
7

The Víctor Grifols i Lucas Foundation was created in 1998 to emphasize the importance of bioethics and foster dialogue among specialists from different areas of knowledge. The Foundation aims to promote bioethics among healthcare organizations, companies and professionals, offering a unique forum to debate and discuss issues related to ethics, science and health care.
Among its range of activities, the Foundation publishes books and articles, organizes ethics-related conferences and events on relevant scientific and social issues, promotes educational initiatives, and awards prizes and research grants.
At the same time, it offers ethical advice to other institutions and co-organizes events with other associations. Its regular collaborators include the Spanish Society of Public Health and Health Administration, Mémora Foundation, Department of Education of the Generalitat de Catalunya, and Friends of UNESCO-Barcelona.
| Scholarships | |
|---|---|
| 6 | |
In 2015, the University of Vic-Central University of Catalonia (UVic-UCC) and the Víctor Grífols i Lucas Foundation joined forces to co-create and develop the Grifols Foundation Chair in Bioethics.
In alignment with its mission, the Chair aspires to promote knowledge in the field of bioethics through teaching and research. The interdisciplinary nature of bioethics requires reflection, both in educational and professional contexts, on the ethics surrounding scientific advances and their social relevance, while respecting life, the individual, dignity, diversity, responsibility and freedom.

"
Over 25 years fostering ethics in biomedicine and health through research, training, and collaboration for responsible scientific development.
Ensuring a reliable plasma supply and promoting self-sufficiency are vital to achieving the company's goal of expanding access to plasma-derived medicines and diagnostic solutions. At the same time, Grifols strives to
lead the industry by exceeding regulatory compliance and setting new benchmarks for quality, safety and transparency.
| S4 CONSUMERS AND/OR END-USERS |
||
|---|---|---|
| Material IROs | Type | Description |
| PERSONAL SAFETY OF CONSUMERS AND/OR END-USERS | ||
| Improved patient well-being | + SP |
Grifols' products and services enhance patients' life expectancy, well-being and quality of life. |
| Quality and safety of products and services |
- SP R |
Grifols guarantees treatment safety and quality through a highly regulated and vertically integrated value chain, complemented by industry best practices. These measures minimize risks or negative impacts while ensuring patients, customers and healthcare professionals remain Grifols' top priority. |
| Increased regulation: stricter health policies and other standards |
R | Grifols monitors and prepares well in advance to address potential regulatory changes. The company leads the development of state-of-the-art production facilities that help set the pace for industry production standards. These combined efforts minimize any risks associated with increases in regulations. |
| INFORMATION-RELATED IMPACTS FOR CONSUMERS AND/OR END-USERS | ||
| Responsible and transparent practices |
+ SP |
Grifols' business model is grounded in ethical and responsible commercial and marketing practices. By providing high-quality information, the company fosters trust among patients, healthcare professionals and society at large. |
| SOCIAL INCLUSION OF CONSUMERS AND/OR END USERS | ||
| Access to treatment and diagnosis | + - R |
Grifols' business model is grounded in ethical and responsible commercial and marketing practices. By providing high-quality information, the company fosters trust among patients, healthcare professionals and society at large. |
| More sustainable healthcare systems |
+ OO |
Grifols collaborates with various countries to help achieve plasma self-sufficiency and ensure access to plasma treatments. The company also operates global industrial fractionation programs to promote the use of hospital plasma, contributing to cost optimization in public healthcare systems. |
| + Positive impact - Negative impact R Risk OO Own Operation SP Supply Chain |
The following policies, actions, metrics and targets enable the efficient management of key IROs related to patients, customers and healthcare professionals.
| Material Sub-topics | Policies | Actions | Metrics and Targets |
|---|---|---|---|
| Personal safety of consumers and/or end-users |
• Patient and Patient Organization Policy • Quality Policy • Patient and Customer Safety Policy |
• Conduct process controls for each batch and final product • Review and monitor production processes • Perform internal and external audits to ensure product quality |
• Maintain the product quality claim rate ≤ 1 claim per 50,000 units sold(1) • Keep the number of critical deficiencies identified in external audits (by Regulatory Health Authorities) below 1. Target set for Biopharma. |
| Information related impacts for consumers and/or end-users |
• Standard Operating Procedure (Grifols Review Process - GRP) for promotional materials • Policy and procedure outlining the transparency program implementation |
• Training on responsible marketing and sales practices • Participation in leading scientific association conferences to enhance learning on products and diseases |
• 18,200 hours of training for sales teams |
| Social inclusion of consumers and/or end users |
• Global Standard Operating Procedure for Grants and Donations to Patient Organizations |
• Developing new procedures for product donations (individual requests) and patient interactions |
• Donation of USD 1 million in critical products and medicines to support emergency relief efforts • Donation of 240 million international units (IU) of coagulation factor medicines to support patients with hemophilia in developing countries • Achieve EUR 18 million annually in charitable donations to support patient-focused programs |

Grifols maintains consistent and open communication with patients and patient organizations (POs), where legally permissible. This includes regular discussions with POs to address areas of mutual interest or concern.
Each business unit also operates claims, pharmacovigilance and surveillance systems to record and evaluate all notifications from healthcare centers, patients or users regarding potential product quality issues.
Each unit has a product recall system with strict procedures to notify health authorities, patient organizations, patients and healthcare professionals about any potential risks associated with recalled products.
Grifols operates a customer service call center and maintains dedicated websites to address inquiries related to the safety, tolerability or efficacy of its products, testament to its commitment to transparency.
In addition to established communication channels designed to maintain open dialogue with patients, patient organizations and healthcare professionals, Grifols positions itself as a reliable and transparent source
*It represents a portion of our sales (around ~82%: IG, FVIII, A-1, Tavlesse and ~35% of albumin used in chronic liver cirrhosis)
USD 29,825 M Dozens
of conditions treated with plasma therapies
Worldwide, more than 3 M people suffer from alpha-1 antitrypsin deficiency, over 6 M have primary immunodeficiencies and more than 1 M live with hemophilia.
We proactively promote access to medicines and support various patient assistance programs
of information for these key stakeholders, in line with its commitment to transparency and independence.
Since 1998, Grifols has supported and participated in the Plasma Protein Therapeutics Association (PPTA) Patient Notification System (PNS). This free and confidential service directly informs registered individuals about voluntary or mandatory withdrawals of plasma-derived medicines.
More details: "Responsible Practices" section in this chapter. More details on main communication channels with stakeholders: "General Information" chapter.
It is estimated that more than two million patients in Europe¹ are affected by one of the 12 most common rare diseases, including hemophilia and primary immunodeficiency (PIDD), which can be treated with plasmaderived therapies.
Furthermore, scientific advancements are expanding the potential of plasma therapies to treat high-prevalence diseases. Plasma proteins are also widely used in routine medical services, emergencies and surgical interventions, among other applications.
| General | Environment | Social Patients and healthcare professionals |
Governance | Annexes | ||
|---|---|---|---|---|---|---|
| MEDICINES 2 | DISEASES AND CONDITIONS TREATABLE WITH PLASMA-DERIVED | |||||
| ALBUMIN • Liver cirrhosis |
• Surgery (cardiac and major procedures) • Intensive care (sepsis, burns, etc.) |
|||||
| • Immunodeficiencies – Primary (PIDD) – Secondary (SID) • Neurological conditions – Myasthenia gravis (MG) |
IMMUNOGLOBULINS – Multifocal motor neuropathy (MMN) • Hematological conditions • Neuromuscular diseases • Post-exposure prophylaxis for rabies • Immunoprophylaxis of hepatitis B |
– Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) – Acute demyelinating polyneuropathy (Guillain-Barré) – Immune thrombocytopenia (immune thrombocytopenic purpura or ITP) • Post-exposure prophylaxis and treatment for tetanus |
ALBUMIN 25 g |
|||
| • Bleeding disorders – Hemophilia A and B |
ALPHA-1 ANTITRYPSIN • Alpha-1 antitrypsin deficiency disorder CLOTTING FACTORS – Von Willebrand disease (VWD) – Rare clotting factor deficiencies • Trauma/injury-related hemorrhaging |
• Overdose of anticoagulants or toxic substances that induce bleeding | IMMUNOGLOBULINS 4g ALPHA-1 ANTITRYPSIN 0.15-0.30g CLOTTING FACTORS Factor VIII:300 a 450 UI Factor IX: 180 a 200 UI |
Plasma-derived medicines have a profound impact by extending life expectancy, improving quality of life and reducing potentially life-threatening complications in individuals with plasma protein deficiencies. These treatments provide significant, life-long benefits to the patients. As a result, most plasma-derived medicines are included in the World Health Organization (WHO) List of Essential Medicines for both adults and children. Many of these medicines are also featured on the EU and U.S. lists of critical medicines.
| Immunodeficiencies and neurological diseases |
Bleeding disorders |
Alpha-1 antitrypsin deficiency |
|
|---|---|---|---|
| Increase in life expectancy |
|||
| Improved quality of life |
|||
| Infection prevention | For IDP and IDS | ||
| Modifies disease progression |
|||
| Prevalence | PIDD: 1/13,500 CIDP: 1/200,000 in children 1 a 7/100,000 in adults PTI: 9.5/100,000 |
Hemophilia A: 25/100,000 Hemophilia B: 5/100000 EvW: 1/8,500- 1/50,000 |
AADT: 123.7/100,000 |

Grifols is committed to building a sustainable and responsible value chain that goes beyond strict regulatory requirements for quality, safety and sustainability. This approach minimizes potential impacts and risks.
By maintaining a highly regulated and vertically integrated value chain, Grifols ensures the safety and quality of its treatments, reaffirming its commitment to prioritize the needs of patients, healthcare professionals and customers.
As a leading company in the healthcare sector, Grifols is dedicated to upholding the highest safety and quality standards for its products and services. This commitment is driven by senior management and endorsed in the Code of Ethics for Grifols Executives. The Chief Quality Officer (CQO) is responsible for overseeing the implementation and maintenance of processes that ensure the quality and safety of all products and services.
Grifols Corporate Quality Policy reflects its firm commitment to these standards, aiming to improve health outcomes and deliver long-term, sustainable value to patients, donors, the healthcare community, collaborators and society as a whole.
Each business unit adheres to policies and procedures designed to guarantee the highest levels of quality, safety and efficiency throughout the value chain. Grifols' quality system spans all operations and includes dedicated policies for continuous employee training and development, empowering them to perform their duties in line with the highest quality and safety standards. The company regularly evaluates its quality systems and processes through various quality committees, where key performance and quality indicators, among others, are closely monitored.
In 2024, Grifols received favorable outcomes from the audits and inspections carried out by global health authorities and organizations, testament to its commitment to quality and safety. In the 2024 fiscal year, Grifols did not identify any impacts or incur any monetary losses related to regulatory non-compliance, fines, notifications or voluntary codes to which it adheres.
Grifols' plasma product quality and safety program is built upon the expertise of its highly trained team, rigorous processes, advanced technologies and complete traceability from plasma donation to market.
All materials and processes are closely monitored throughout the supply chain by Grifols' quality department. This includes process controls and batch-by-batch monitoring of final products, as well as the review and supervision of production processes to ensure compliance with Good Manufacturing Practices (GMP). Systems are in place to escalate relevant events and implement appropriate measures through established Quality Committees, where key performance and quality indicators are regularly assessed. All medical devices are evaluated to comply with the European REACH regulation (Registration, Evaluation, Authorization, and Restriction of Chemicals).
Grifols is a member of the National Donor Deferral Registry (NDDR), a voluntary self-regulation initiative to guarantee the safety and quality of donated plasma through strict standards its donors must adhere to.
External entities certify the quality systems of all Grifols' production plants, including the manufacture of its medicines and medical devices.
Good Manufacturing Practices (GMP) certifications from the European Union, United States and other countries requiring GMP compliance.
Plasma Protein Therapeutics Association (PPTA) IQPP & QSEAL certifications
International Quality Plasma Program (IQPP) certifications: a voluntary program for plasma collection, including donor management and plasma center operations.
Grifols' management team defines and maintains the quality management system, including routine in-house audits of plasma centers, laboratories, production facilities and warehouses to monitor quality standards and ensure compliance with applicable regulations.
The Quality Audit Department conducts routine reviews of all operations.
All plasma centers, manufacturing plants, warehouses and laboratories are regularly inspected by health authorities in the United States (FDA), Europe (EMA) and other countries in compliance with their respective regulations.
Plasma centers and fractionation plants are also subject to regular audits by the Plasma Protein Therapeutics Association (PPTA).
Internal audits 236 (Grifols) 7 (Biotest)
Inspections by health authorities and accredited inspection entities 450 (Grifols) 11 (Biotest)
Favorable supplier audits 61 (Grifols) 11 (Biotest)
Internal audits 58 (Grifols) 12 (Biotest)
Inspections by health authorities and accredited inspection entities 22 (Grifols) 2 (Biotest)
Favorable supplier audits 136 (Grifols) 46 (Biotest)
DIAGNOSTIC
53 Internal audits
13 Inspections by health authorities and accredited inspection entities
24 Favorable supplier audits
OTHERS****
94 Internal audits
25 Inspections by health authorities and accredited inspection entities
62 Favorable supplier audits
BIO SUPPLIES
1 Internal audits
11 Inspections by health authorities and accredited inspection entities
0 incidents related to suspension, revocation or loss of any license or certification; warning letter, imposed suspension of any regulated activity
| Grifols | Plasma Procurement: 412 Biopharma: 14 Diagnostic: 13 Others: 22 Bio Supplies: 10 |
||
|---|---|---|---|
| Biotest | |||
| Plasma Procurement: 9 Biopharma: 10 |
|||
| in-house inspections. Includes Grifols and Biotest. *Former Bioscience Division. |
**** Others: includes Former Hospital Division. | * Includes inspections by health authorities and accredited inspection bodies, as well as |
Grifols' Supplier Qualification Management System ensures that all raw materials, including plasma from external suppliers and critical nonplasma suppliers, undergo a rigorous, continuous evaluation process. Grifols conducts a comprehensive program of routine supplier audits to ensure compliance with GMP regulations and quality standards across all its business units.
390+ quality control supplier audits performed in 2024
| Type of supplier | Result | |||||
|---|---|---|---|---|---|---|
| Business unit/Area | No. of quality audits |
Favorable | Not favorable |
Pending evaluation and final report |
||
| Raw materials suppliers | 40 | 39 | 0 | 1 | ||
| Plasma Procurement | Distributors | 5 | 5 | 0 | 0 | |
| and Bio Supplies | Transport companies | 2 | 2 | 0 | 0 | |
| Service suppliers | 15 | 15 | 0 | 0 | ||
| Raw materials suppliers | 97 | 95 | 2 | 0 | ||
| Distributors | 3 | 3 | 0 | 0 | ||
| Biopharma | Transport companies | 10 | 10 | 0 | 0 | |
| Service suppliers | 28 | 28 | 0 | 0 | ||
| Raw materials suppliers | 19 | 17 | 0 | 2 | ||
| Distributors | 4 | 4 | 0 | 0 | ||
| Diagnostic | Transport companies | 0 | 0 | 0 | 0 | |
| Service suppliers | 5 | 3 | 0 | 2 | ||
| Grifols global subsidiaries |
Raw materials suppliers | 0 | 0 | 0 | 0 | |
| Distributors | 14 | 14 | 0 | 0 | ||
| Transport companies | 17 | 17 | 0 | 0 | ||
| Service suppliers | 17 | 17 | 0 | 0 | ||
| Others | Raw materials suppliers | 48 | 48 | 0 | 0 | |
| Distributors | 3 | 2 | 1 | 0 | ||
| Transport companies | 1 | 1 | 0 | 0 | ||
| Service suppliers | 11 | 11 | 0 | 0 |
| Plasma Procurement | Raw materials suppliers | 0 | 0 | 0 | 0 |
|---|---|---|---|---|---|
| Distributors | 0 | 0 | 0 | 0 | |
| Transport companies | 0 | 0 | 0 | 0 | |
| Service suppliers | 11 | 11 | 0 | 0 | |
| Biopharma | Raw materials suppliers | 20 | 20 | 0 | 0 |
| Distributors | 9 | 9 | 0 | 0 | |
| Transport companies | 3 | 3 | 0 | 0 | |
| Service suppliers | 14 | 14 | 0 | 0 |
As outlined in its Quality Policy, Grifols identifies the critical attributes of its products and conducts thorough quality controls on raw materials, manufacturing processes and finished product testing.
Grifols establishes quality agreements with all distributors, which include specific provisions on pharmacovigilance and vigilance, including those operating in countries with less advanced pharmacovigilance or surveillance regulations. These agreements clearly define the responsibilities in this area to ensure that Grifols' rigorous standards are upheld.
The company has also implemented a pharmacovigilance system to monitor any adverse reactions or effects resulting from its medicines, as well as a surveillance system to track adverse incidents due to the use of medical devices and in vitro diagnostic medical devices. Under these programs, Grifols operates a reporting system for suspected adverse reactions, effects or incidents that may pose a safety concern.
All activities and requirements of the pharmacovigilance and surveillance systems for medical devices and in vitro diagnostic devices are detailed in Grifols' standard operating procedures, which are regularly updated to comply with applicable regulations in every country where Grifols distributes its products. The company conducts regular internal audits of both systems as part of its quality compliance framework, and both systems are subject to external inspections by the relevant health authorities.
Grifols does not outsource primary pharmacovigilance or medical device surveillance and in vitro medical devices activities to third parties. However, certain minor activities specific to the pharmacovigilance of Biopharma products have been outsourced.
Grifols' claims system, as described in its corporate policy, records and evaluates all notifications received from employees, healthcare centers, patients and users regarding concerns about potential product quality issues. For medical devices, the management system for technical services is integrated with the complaints management system to ensure all customer requests are properly assessed.
When a subsidiary or authorized call center receives a complaint about a product or service marketed by Grifols, it immediately notifies the relevant manufacturing plant. This process ensures that all complaints are thoroughly evaluated in accordance with the established claims system.
The quality department of each business unit oversees the claims process, which includes conducting the relevant investigations; verifying the implementation of corrective and preventive actions, if necessary; notifying relevant health authorities, if applicable; and informing the customer of the findings from the claim investigation.

1 per 75,186 units distributed
2023: 1 per 97,895 units distributed
1 per 170,224 diagnostic tests 2023: 1 per 559,298 diagnostic tests
1 per 1,651 units distributed 2023: 1 per 2,777 diagnostic tests
1 per 3,692,028 units distributed 2023: 1 per 14,972,662 units distributed
1 per 114,835 units distributed 2023: 1 per 50,005 units distributed
1 per 103,114 units distributed 2023: 1 per 77,777 units distributed

The product recall system is governed by Grifols' corporate policy on patient and customer safety.
This system is developed through standardized operating procedures and is subject to internal audits to ensure its effectiveness and compliance with current regulations. It is also regularly inspected by the competent health authorities.
All Grifols teams involved in potential product recalls, whether voluntary or mandatory, receive specialized training in the proper management of these incidents. Grifols also conducts periodic product recall simulations to test crisis management procedures and protocols, as well as identify and address potential areas for improvement.
The product recall system includes specific procedures for notifying health authorities, patient organizations and healthcare professionals about any potential risks associated with recalled products. Grifols operates a call center and maintains dedicated websites for certain products to communicate potential risks. The use of recalled products in clinical trials is strictly prohibited.
In the past four years, Grifols and Biotest did not have any mandatory product recalls (Class I, II, or III) due to quality or safety issues. In 2024, Grifols has not carried out any voluntary product recalls.
Strict controls ensure that quality and safety standards are fully complied with, and the processes in place facilitate a swift and effective recall if necessary. In this regard, in 2024, a counterfeit Biotest Albiomin (albumin) product was detected, which even included a forged local authority seal to appear authentic. Although the original Biotest drug did not present any quality defects, the company decided to recall the affected batch from the market as a measure to help eliminate the counterfeit product, in addition to launching an information campaign. Both actions were carried out in collaboration with the competent authorities to protect patient safety.
The counterfeiting of medicines and advanced diagnostic systems poses a global risk to patient safety and public health. Plasma-derived medicines are typically prescription-only drugs and are primarily administered in hospital settings.
Grifols collaborates with regulatory authorities to investigate and analyze suspected cases of counterfeit products. The company has implemented an Anti-Counterfeiting Policy to help prevent, detect and report counterfeit products. Under this policy, any suspected or confirmed cases of counterfeit medicines must be promptly reported to the relevant regulatory authorities in compliance with applicable regulations.
Committed to supporting regulatory authorities in preventing counterfeiting, Grifols uses track-and-trace technology to comply with product serialization and aggregation requirements in certain countries and regions. Beyond these obligatory measures, Grifols implements additional anti-counterfeiting safeguards, including assigning unique codes to vials before marketing any plasma-derived product and adding holographic seals to packaging to ensure its integrity and authenticity.
Grifols undergoes regular internal audits and external inspections to verify compliance with applicable regulations and conducts due diligence with customers and distributors to confirm they hold the necessary licenses to distribute its products.
Furthermore, Grifols outlines detailed measures for addressing suspected counterfeiting in its contracts and quality agreements with third parties, where applicable. Since 2021, Grifols has not been aware of any incidents leading to raids, seizures, arrests or the filing of criminal charges related to counterfeit products.
General Environment Social Governance Annexes Patients and healthcare professionals
By integrating the knowledge, experience and perspectives of patients, patient organizations, healthcare professionals and healthcare organizations, Grifols is able to develop increasingly innovative and personalized treatments, diagnostics, technologies, services and solutions.
Patient associations and organizations play a vital role in global healthcare systems. They contribute to patient education, advocate for patient rights and support clinical research. At Grifols, these organizations increasingly influence decision-making. Actions and initiatives involving these groups are coordinated and managed by the Global Patient Affairs team.
All collaborations with patient associations adhere to the applicable principles of transparency and the specific regulations of each country. Grifols has implemented standardized operating procedures that internally govern collaboration agreements, grants and donations, ensuring they meet criteria of eligibility, compliance, ethics and transparency.
These general principles and commitments are outlined in the Policy for Patients and Patient Organizations and other internal procedures. Grifols also publishes annual, country-specific reports detailing the support provided and value transfers made to patient organizations worldwide.
Grifols' collaborations include educational initiatives on the unique nature of plasma-derived medicines and the complexity of their production processes; joint advocacy efforts to promote better patient access to plasma-derived medicines; and support initiatives, combining employee volunteer efforts and financial resources, all in compliance with current regulations and laws.
Grifols engages with approximately 70 patient organizations across key therapeutic areas globally. In 2024, the company allocated more than EUR 18.6 M to product donations and EUR 9.14 M support for around 60 patient associations worldwide, funding various programs and activities. Much of this effort was concentrated in Europe, in an aim to foster greater engagement and contribute to the professionalization of these organizations.
Therapeutic areas / diseases
4 geographic areas
North America, focus on the United States and Canada
Europe, focus on Spain, France, Germany, Italy, the United Kingdom and Nordic countries
Latin America: focus on Brazil and Argentina
Asia-Pacific: focus on Australia
Through the Patient Organization Donation Program, Grifols supports projects and initiatives aligned with four strategic priorities:
Education and empowerment: Grifols helps patients become actively involved in decisions about their health. For rare diseases, educating the medical community is also crucial. The company collaborates in various seminars and scientific conferences to advance this goal.
Awareness and visibility: giving greater visibility to patient communities fosters a sense of solidarity and helps bring their needs and challenges onto the political agenda. Grifols contributes by supporting the creation and maintenance of different channels of communication and educational materials.
Experience and well-being: Grifols supports projects that contribute to improved disease management and enhance patient experience. In 2024, the company supported psychosocial programs led by patient organizations in different therapeutic areas to promote a holistic approach to care.
Patients and healthcare professionals
In 2024, Grifols promoted various educational initiatives with patient communities in Europe. As part of the "Plasma Awareness Educational Program," webinars were organized with representatives from these communities to inform and update them on policies that impact their lives.
Additionally, new visits to Grifols facilities were arranged locally, offering participants insights into the company's operations and commitment to plasma-derived medicines. Grifols also launched a program that enables patients to share their firsthand experiences and testimonies. This initiative aims to give all employees an opportunity to learn from and connect with patients, fostering a deeper understanding of the company's mission.
Grifols' interactions with healthcare professionals and organizations contribute to enriching its knowledge and expertise on patient behavior and disease management. This is critical to guiding industry efforts and enhancing the quality of patient care and treatment options. All interactions are conducted with maximum integrity and transparency, regulated by Grifols' Global Compliance Program.
Grifols' Gifts and Hospitality Policy provides clear guidance for employees on the appropriate standards and established limits for managing transfers of value and hospitality to healthcare professionals, public officials and other individuals.
The U.S. Sunshine Act (PPS) requires manufacturers and group purchasing organizations (GPOs) of pharmaceuticals, biologicals and medical devices to itemize all information relating to payments and transfers of value made to specific healthcare professionals and organizations, including physicians, advanced practice providers and teaching hospitals. The Centers for Medicare and Medicaid Services (CMS) publishes these reports annually in June.
Grifols has established policies and procedures to manage its transparency program, ensuring compliance with U.S. federal and state reporting obligations. The company adheres to the Pharmaceutical Research and Manufacturers of America (PhRMA) and Advanced Medical Technology Association (AdvaMed) Codes on Interactions with Healthcare Providers. Last updated in January 2022 (PhRMA) and June 2022 (AdvaMed), these codes aim to reinforce ethical standards and principles in interactions with the healthcare community.

Under the Open Payment Program, transfers of value in the U.S.
In line with these principles, Grifols may engage healthcare professionals such as consultants or advisors, provided they are selected based on their qualifications and expertise to meet a specific need. Financial compensation must reflect fair market value for the services provided, and all arrangements must be formalized through written contracts.
Grifols provides a transparency-training program for all employees whose roles require regular interaction with U.S. healthcare organizations and professionals. In total, 62 U.S.-based employees participated in formal transparency-specific training, while the North American Healthcare Compliance team provided information and individual instruction throughout the year to a broader group of employees. These training efforts are designed to ensure that all employees involved in such interactions fully internalize and comply with transparency regulations and ethical principles.
In 2015, Grifols voluntarily adopted transparency practices in Europe4 in alignment with Chapter 5 of the European Federation of Pharmaceutical Industries and Associations (EFPIA) Code, extending them to all corporate divisions and operations.
In 2024, for the ninth consecutive year, Grifols disclosed all payments and other transfers of value related to medicines and healthcare technology made to professionals and organizations in various European countries covered under the EFPIA Code. The company also has a policy and procedure in place that outlines how its transparency program is implemented to comply with the Code.
In accordance with EFPIA criteria in Europe
EUR 14.5 M in 2023 -34% vs 2022 69% transfers of value related to R&D
As a member of MedTech Europe, Grifols applies the transparency guidelines outlined in its Code of Ethical Business Practice, including reporting the Training Grants conducted in 2023. Additionally, Grifols publishes detailed information on country-specific transfers of value, in compliance with local regulations. The company also maintains its own policy and procedure to ensure compliance with reporting obligations required by U.S. state and federal government agencies.
The information included in product packaging, leaflets and labels adheres to the applicable standards and regulations in every country where Grifols operates, including Good Manufacturing Practices (GMP) for medicines.
For medical devices and in vitro diagnostic medical devices, the labelling, reagent instructions for use and user manuals for instruments and software, comply with country-specific regulations, (EN ISO 15223, among others) and incorporate mitigation measures identified through medical device risk management systems (EN ISO 14971) or as required by health authorities. All printed materials are translated into the relevant languages, regularly updated as needed and made easily accessible to users.
| 2023 | 2022 | 2021 | ||||
|---|---|---|---|---|---|---|
| EUR | % | EUR | % | EUR | % | |
| Services | 1,415,862 | 10% | 1,294,739 | 7% | 1,006,669 | 5% |
| Contributions to professional healthcare events |
601,717 | 4% | 293,171 | 1% | 57,272 | 0% |
| Contributions to cover costs of healthcare events |
2,306,191 | 16% | 2,505,772 | 13% | 1,978,053 | 11% |
| Grants | 197,343 | 1% | 628,962 | 3% | 280,272 | 1% |
| Third-party R+D collaboration | 10,021,128 | 69% | 14,779,095 | 76% | 15,609,633 | 83% |
| TOTAL | 14,542,241 | 100% | 19,501,739 | 100% | 18,931,899 | 100% |
| 2023 | 2022 | 2021 | ||||
|---|---|---|---|---|---|---|
| USD | % | USD | % | USD | % | |
| Services | 1,361,895 | 33% | 935,321 | 17% | 4,128,833 | 34% |
| Contributions to professional healthcare events |
843,366 | 20% | 645,974 | 11% | 344,243 | 3% |
| Grants | 0 | 0% | 0 | 0% | 0 | 0% |
| R&D collaborations with third parties | 1,383,432 | 34% | 3,058,171 | 54% | 7,025,507 | 59% |
| Investigator sponsored research | 524,084 | 13% | 1,023,755 | 18% | 483,866 | 4% |
| TOTAL | 4,112,777 | 100% | 5,663,221 | 100% | 11,982,449 | 100% |
| 2023 | 2022 | |||
|---|---|---|---|---|
| EUR | % | EUR | % | |
| Services | 252,022 | 9% | 264,091 | 2% |
| Contributions to professional healthcare events | 251,262 | 9% | 240,973 | 2% |
| Contributions to cover costs of healthcare events | 373,269 | 13% | 8,455,016 | 77% |
| Grants** | 195,000 | 7% | 304,000 | 3% |
| Third-party R&D collaborations | 1,694,314 | 61% | 1,747,144 | 16% |
| TOTAL | 2,765,868 | 100% | 11,011,226 | 100% |
*Transfers of value in Europe as defined by the EPFIA Disclosure Code. ToVs included with one-year intervals.
**Includes research grants. Research data as defined by the EPFIA Disclosure Code do not reflect the company's entire R&D investment. Biotest data includes information from the Biotest AG group under Biotest Compliance supervision.
Grifols ensures that all marketing activities, as well as promotional and educational materials, comply with applicable laws and regulations; align with industry policies and codes voluntarily adopted by the company; adequately address the target audience and end-users and provide accurate, reliable, comprehensive and balanced information.
The company follows a standard operating procedure (SOP) to define the responsibilities and processes for the approval, review and control of all marketing initiatives. This includes participation in congresses and the design and distribution of promotional and educational materials about Grifols' products and services.
The Grifols Review Process (GRP) guides the management and approval process to be followed for all marketing materials. Representatives from the legal, medical and regulatory departments review and approve this material using an electronic system which has been specifically designed for the GRP process, in order to guarantee that these are aligned with responsible marketing practices.
All marketing material and content is approved for specific uses in designated countries and may only be used with no alterations. The contents of all promotional and educational materials are routinely reviewed to ensure compliance with current regulations and codes in force. Grifols also provides training on responsible sales and marketing practices in line with the company's Code of Conduct and Anti-Corruption Policy.
In 2024, Grifols received 3 marketing complaints, which were dealt with in accordance with established procedures. These complaints had an economic impact of EUR 12,000. Biotest has not received any complaints related to marketing.


The World Health Organization (WHO), the Council of Europe and other institutions stress the importance of achieving self-sufficiency in plasmaderived medicines to give patients adequate access to these essential treatments.
Specifically, the WHO Resolution WHA 63.12 urges member states to establish, implement and support sustainable blood and plasma collection programs. When efficiently managed and nationally coordinated in accordance with the available resources in each country, these programs enable increased self-sufficiency. However, WHO figures show that only 56 out of 171 reporting countries produce plasma-derived medicines by fractionating plasma collected domestically, while 91 countries report relying entirely on imports for plasma-derived medicines.
Currently, EU countries face a plasma shortfall of 5.4 million liters required to meet treatment demands. Plasma collected in Europe accounts for only 63% of the volume needed to produce essential plasma medicines, while the remaining treatments–primarily manufactured using U.S. plasma–are imported. This heavy reliance on third countries heightens the risk of shortages, as witnessed in 2021 following the COVID-19 pandemic. Such shortages may lead to these medicines being rationed and unjustified delays in treatment. For example, in Spain, the self-sufficiency gap for immunoglobulins stands at 36%.
Grifols is committed to promoting and improving access to treatments for patients by supporting and working with countries to help them increase their levels of self-sufficiency, thereby strengthening their healthcare systems and limiting dependence on third parties. The company is leading this change through the Grifols Self-Sufficiency Program. Furthermore, its global industrial plasma fractionation programs contribute to improving healthcare costs, promoting better and greater access to plasma treatments and contributing to more sustainable healthcare systems.
Grifols reached a long-term collaboration agreement with Canadian Blood Services (CBS) in 2022 to accelerate the country's immunoglobulin (Ig) self-sufficiency from 15% to 50% in the shortest timeframe possible, reducing the volume of plasma-medicine imports.
In 2024, Grifols continued to make significant progress in consolidating a vertically integrated supply chain to meet the needs of Canadian patients. This supply chain includes newly established donation centers and the production facilities in Montreal. Until the Montreal plant becomes fully operational in 2027, production is being carried out at Grifols' facilities in Clayton, North Carolina (USA).
In 2020, Grifols began developing the first integrated platform in the Middle East and Africa to supply plasma therapies at national and regional levels as part of its strategic alliance with the Egyptian government. Through this collaboration, the company will promote Egypt's self-supply of plasma medicines through a pioneering publicprivate partnership.
Grifols actively promotes patient access to treatments, particularly when extraordinary circumstances may limit or disrupt access. Since 2006, the company has implemented initiatives in the U.S. to support patients treated with its plasma-derived medicines without health insurance. Grifols also offers treatments for patients in need of temporary assistance and promotes comprehensive support programs to help patients manage their diseases effectively.
Grifols provides direct support to patients who, due to exceptional circumstances, are unable to access treatments.
17,000+ patients have had access to free products or services
An estimated 400,000 people around the world suffer from severe hemophilia, yet 75% remain untreated. Grifols, to address this issue, began collaborating with the World Federation of Hemophilia (WFH) Humanitarian Aid Program in 2014, donating clotting factors for hemophilia patients in need of treatment. Grifols' donations also support the WFH's Global Alliance for Progress (GAP) program. In its second decade, this initiative aims to increase the number of patients diagnosed and treated for bleeding disorders, especially in developing countries.

Grifols' 2022-2030 Commitment to the World Federation of Hemophilia includes the donation of

AlfaCare is a holistic support program for patients with Alpha-1 Antitrypsin Deficiency (AATD) offering training, emotional support and guidance to help them effectively manage their condition by promoting new habits to enhance their physical, dietary and psychological well-being. The program was launched in Spain in 2018 with the collaboration of the Alfa-1 Spain Association and the support of a multidisciplinary clinical team including psychologists and patient mentors. Since then, the program has expanded to Germany under the name AlphaCare and to Italy as GriCare.
AlfaCare has proven to deliver significant value to AADT patients. As of December 2024, it supports 265 patients in Spain, who receive psychological support and respiratory physiotherapy, among other services, and 32 of them receive home treatment. In Germany, the program supports 744 patients and in Italy, 110 patients.
Programa AlfaCare
1,000+ patients supported across 3 countries
Grifols collaborates with Direct Relief, a humanitarian organization operating in over 80 countries, to provide healthcare professionals with medical resources following natural disasters and other humanitarian or poverty-related emergencies. This partnership ensures the availability of donated products in the shortest possible time.
Value of medicines donated 2019-2024 EUR 2.74 M
Value of medicines donated in 2024 EUR 0.04 M
Patients treated in 2024 3,245+
Units of products donated in 2024: 2,800+

Accurate and timely diagnosis is the first critical step toward effective prevention and treatment, directly impacting patient safety. Grifols specializes in transfusion and personalized diagnostic solutions aimed at reducing diagnostic errors. According to the WHO,1 such errors may include delays in diagnosis, incorrect diagnosis, missed diagnosis or failure to communicate the diagnosis, all of which can occur at any stage of the diagnostic process.
Through its Diagnostic division, Grifols drives continuous innovation to provide blood and tissue banks with highly sensitive and specific tests to ensure safe transfusions and donations. Grifols assays are based on nucleic acid amplification techniques (NAT), which enable the detection of viruses such as HIV, hepatitis B and C, as well as emerging viruses like Zika and West Nile, and parasites such as those that cause babesiosis.
Grifols also develops blood typing platforms to ensure compatibility between donors and recipients. These gel-based assays not only identify major blood groups like ABO and Rh but also detect less common blood groups that are still highly relevant to human pathologies, such as sickle cell anemia and cancer.
According to the World Health Organization (WHO), 50% of donated blood is collected in emerging countries, which account for 80% of the global population¹. These countries lack basic measures to ensure safe transfusions and donations are not universally implemented. Grifols is actively working to expand its transfusion diagnostic solutions in emerging markets, including the Philippines, India, Egypt and Indonesia. This is also the case in China, where Grifols collaborates with Shanghai RAAS to progressively contribute to raising transfusion safety standards in the country's blood donation centers.
In 2024, Grifols' NAT technology was used to test more than 38 million blood donations, and the company supplied over 71.5 million gel-based blood typing cards.
In 2023, Grifols launched the AlphaID™ At Home Genetic Health Risk Service, the first free, direct-to-consumer program for U.S. residents designed to facilitate genetic detection of Alpha-1 Antitrypsin Deficiency (AATD). This condition, which has symptoms similar to COPD, is estimated to affect about 1 in every 2,500 Americans.
Using AlphaID™ At Home, individuals can assess their risk of developing lung and/or liver disease associated with Alpha-1 using a simple saliva sample, without needing to visit a healthcare professional.
As of May 2024, nearly 68,000 AlphaID™ At Home kits had been requested. Additionally, the AlphaID™ kit, developed by Progenika, has been used in medical practices and across many other countries, enabling the detection of AATD and helping patients take appropriate steps to address this health condition.
In the European Union, Latin America and Turkey, some 35,000 units were distributed free of charge during 2024.
Grifols is also focused on developing new diagnostic tests for personalized medicine, aimed at prognosis, predicting responses, and monitoring biological therapies. Furthermore, the company is advancing molecular diagnostic and prognostic tests in areas such as oncology, autoimmunity, cardiovascular medicine and central nervous system disorders.

Outside of its core activity, Grifols shares its expertise with other countries by making its facilities, technology, expertise and technical teams available to donation centers and public health organizations. This includes processing surplus plasma, purifying the proteins and returns them entirely in the form of plasma-derived medicines.
Regulated by plasma fractionation service agreements, these public-private collaborations provide healthcare administrations with significant cost savings on plasma-derived medicines. These collaborations are offered in Spain, Italy and Canada. In 2023, Grifols extended this service to Egypt, supporting efforts to promote the country's self-sufficiency in plasma-derived medicines.

More details: "Access to Medicines" section.

This broad-based service is customized to each client (public and private entities) and covers the entire plasma logistics chain, including collection, transportation, testing, analysis, fractionation, purification, dosing and delivery of finished products.
This solution includes, among others, the Quality Program to advise on quality management and assurance systems and the Academy Program offering plasma-related training activities, courses and programs. Simultaneously, the Grifols Plasma Management Service web solution was developed by Grifols to improve, streamline and facilitate communication among the various parties involved in monitoring the industrial plasma fractionation contract and guarantee full traceability during the process.
Grifols spearheads a range of additional services to support and address the needs of blood banks, working collaboratively to promote plasma self-sufficiency.
Human plasma has become a strategic resource for Spain's National Health System, serving as an essential raw material for the production of plasma-derived medicines. Increasing plasma donations through apheresis is a top priority, with efforts concentrated on expanding the plasma donor pool.
In 2024, numerous groups worked to increase the volume of plasma collected in Spain to benefit thousands of patients. For the fourth consecutive year, these collective efforts have surpassed 400,000 liters of plasma collected for fractionation and the production of plasma-derived medicines. This volume represents between 40% and 60% of the plasma required to produce the plasma therapies needed in the country.
Grifols leads the way to actively support awareness campaigns aimed at promoting plasma donations in Spain.
| Collaborative solutions |
Safety throughout the supply chain |
Comprehensive production quality control |
Increased self-sufficiency |
Patient-focused | Savings for healthcare systems |
|---|---|---|---|---|---|
| ---------------------------- | ------------------------------------------ | ------------------------------------------------ | ------------------------------- | ----------------- | -------------------------------------- |
Innovation at Grifols focuses on four key priorities: accelerating the development of new therapies, products and services, and driving ongoing improvements and new indications for existing ones; promoting competitiveness; optimizing in-house productivity to achieve greater efficiencies; and supporting scientific cooperation, education and research capabilities to advance scientific knowledge.
In this context, Grifols provides specific information about its innovation efforts to facilitate a broad-based understanding of the company as a whole.
| Material IROs | Type | Description | ||
|---|---|---|---|---|
| INNOVATION | ||||
| Clinical trials | - SP OO |
Grifols firmly believes that advances in life sciences must be rooted in a humanistic and ethical approach. The company is committed to protecting the rights, safety and well-being of patients involved in the clinical trials it leads or sponsors. The company also advocates for the responsible and ethical use of laboratory animals in trials essential for the development of life-saving therapies. |
||
| Promoting knowledge and research for the benefit of society |
+ OO |
Grifols promotes research and scientific progress to contribute to the advancement of society. The company offers a differential innovation portfolio, focused primarily on developing treatments and diagnostic solutions. These efforts are further strengthened by the use of artificial intelligence (AI), which has the potential to drive significant breakthroughs via the analysis of clinical trial data and plasma donor information. At the same time, it strives to integrate sustainability criteria into its product innovation to foster both social progress and environmental protection. |
||
| Improvement of production processes |
R O |
Grifols recognizes the transformative power of technological advances to optimize the production processes of plasma-derived medicines and improve operational logistics, driving both revenue growth and cost reduction. The company has started to explore and integrate AI solutions to boost efficiency and productivity, and ultimately achieve significant cost savings. Grifols is also positioning itself in future-forward segments including recombinant medicines and antibody therapies, which may lead to new opportunities and strengthen its long-term competitive advantage. |
||
| Investment in new technologies | R | Technological innovation offers Grifols the opportunity to optimize its production processes and enhance its competitiveness in its industries of operation, ensuring a sustainable future. The company proactively anticipates its investment needs, both from a financial and human resources perspective. |
The following policies, actions, metrics and targets enable Grifols to efficiently and effectively manage the key material IROs related to innovation in alignment with its current reality.
| Material Sub-topics | Policies | Actions | Metrics and Targets |
|---|---|---|---|
| Innovation | • Human Rights Policy • Animal Welfare Policy |
• Deliver excellence in innovation by expanding the focus on platforms (plasma and non plasma), therapeutic areas and internal and external knowledge to benefit a larger number of patients |
• Achieve more than 80% of the defined milestones in innovation projects • Assign at least 75% of R+D investments to products and market expansion |
Effective communication with stakeholders in science, technology and innovation is essential for promoting the development and promulgation of new ideas and projects. Grifols' two-pronged innovation scope fosters knowledge sharing and communication both internally and externally, giving the company a strategic edge. This approach not only informs but also actively engages and connects key players within its innovation ecosystem, helping it advance progress, anticipate changes and build a support network to boost competitiveness.
On an internal level, digital transformation committees and R&D+i project analysis forums are the primary platforms for addressing key innovationrelated issues–including critical material matters–across the organization.
Externally, academic collaborations with centers of excellence and coinnovation programs are vital communication channels for the exchange of ideas and knowledge.


*Includes Biotest data.
Innovation is at the core of Grifols' operations and embedded in its DNA. The company promotes the development of healthcare solutions through substantial investments in both financial resources and talent, leveraging its network of research hubs in the U.S. (California and North Carolina) and Europe. Furthermore, Grifols boasts advanced research platforms that reinforce its leadership in biomedicine. These platforms, along with its investees, will enable the company to continue improving the lives of millions and anticipate the future of medicine.
GigaGen U.S.: dedicated to the discovery and development of recombinant polyclonal antibody-based drugs to treat immunodeficiencies, infectious diseases and immunotherapy-resistant cancers
Grifols investee company
For Grifols, advances in life sciences should never be severed from their intrinsic humanistic component. The relevance of ethics in biomedical and technological innovation is paramount to guiding the responsible and sustainable development of science and technology, ensuring these advancements are used for the benefit of humanity. In this regard, scientific progress should always emerge from an ethical and social construct.
Grifols translates this commitment into action through the Víctor Grífols i Lucas Foundation. Among their competencies, the review committees within the Grifols Scientific Innovation Office oversee and manage all matters related to clinical trials, including those with ethical ramifications.
The company adheres to three fundamental and universal principles that guide the ethical considerations of its clinical trials, as outlined in its Human Rights Policy.
We subscribe to three fundamental and universal principles:
RESPECT FOR PEOPLE: Respect for an individual's ability to make decisions freely and independently, and protection of vulnerable groups of people who participate as research subjects. This principle is expressed through informed consent forms.
WELFARE: Guarantee the health of people who participate in clinical trials. Risks must be minimized and benefits maximized for all participants. For Grifols, protecting people's health takes precedence over professional and personal interests, research advances and the search for knowledge.
JUSTICE: Research must strike a balance between benefits and risks. All subjects must be treated with equal consideration, with no discrimination in the selection of subjects. Under this principle, participants are never exposed to unsafe situations to benefit another person. There is an obligation to safeguard the rights of vulnerable groups.
Clinical trials are essential for advancing medical knowledge and providing innovative medications to individuals with specific diseases or conditions.
Grifols is committed to protecting the rights, safety and well-being of patients who participate in the clinical trials it leads or sponsors. All clinical research led by Grifols or on its behalf adheres to the standards defined in the International Conference on Harmonization of Technical Requirements for Pharmaceutical Products for Human Use regarding Good Clinical Practice (ICH GCP); the protection of human beings under the Declaration of Helsinki (1964); and applicable local laws and regulations.
Clinical trials are described in a detailed protocol, which is submitted to regulatory authorities and external ethics committees for their evaluation. They only begin once a favorable decision has been handed down.
Participants submit a written, signed and dated informed consent form. The lead researcher (or assigned healthcare professional) provides appropriate information, resolves any doubts and gives potential clinical-trial subjects sufficient time to make an informed decision on their participation.
In order to maintain quality control, Grifols has standard operating procedures that guarantee that the clinical trial and its related trial data are documented and communicated data according to protocol, ICH GCP principles and applicable regulatory requirements. In addition, Grifols has detection procedures in place that allow clinical professionals to detect and document possible fraud or misconduct in clinical trials.
Several measures at Grifols ensure the transparency of data collected in its clinical trials while safeguarding the anonymity of trial subjects and the protection of their personal data in accordance with the General Data Protection Regulation (GDPR). Grifols also subscribes to the principles of the codes of conduct regulating the treatment of personal data from clinical trials and other applicable clinical and pharmacovigilance research.
Information on the protocol, status of clinical trials and their results are disclosed on publicly accessible registries, including www.clinicaltrials.gov
In addition, the results of trials conducted in Europe are published in the EudraCT (European Union Drug Regulating Authorities Clinical Trials Database) when the trial is regulated by Directive 2001/20/EC, and the Clinical Trials Information System (CTIS) platform when the trial is governed by Regulation 536/2014.Grifols also publicly shares the results of many of its clinical trials at international conferences and in scientific journals.
Grifols is committed to the responsible use of laboratory animals when required for the development of new life-sustaining therapies.
Whether studies are carried out in university settings or in external laboratories, Grifols researchers work closely with regulatory agencies and the Institutional Animal Care and Use Committee (IACUC) to guarantee the safe and ethical treatment of animals.
All facilities are approved by the competent authorities where research is conducted. In the U.S., Grifols facilities are certified by the Association for Assessment and Accreditation of Laboratory Animal Care (AAALAC) or equivalent organization, and hold the highest accreditation possible for animal-testing laboratories.
All European laboratories comply with Directive 2010/63/EU concerning the protection of animals used for scientific purposes and are assessed by the competent authorities of each country. Grifols research adheres to the "Alternatives and the 3Rs" (Replacement, Reduction and Refinement) protocol, which advocates (i) Replacing the use of animal-testing with alternative techniques or avoiding it completely; (ii) Reducing the number of animals used; and (iii) Refining how experiments are performed to ensure animals suffer as little as possible.
More information: ClinicalTrials.gov and EudraCT
Grifols promotes research and scientific progress to contribute to the advancement of society. Accelerating and advancing new plasma-derived and non-plasma treatments and indications is critical in the company's ongoing efforts to generate a positive impact on patients and society.
To this end, Grifols has a differential product portfolio centered on six core therapeutic areas, while also supporting and integrating projects spearheaded by Biotest, Alkahest, Araclon and GigaGen.
| Pre-clinical | Phase 1 | Phase 2 | Phase 3 | Phase 4 | Regulatory | LCM | ||
|---|---|---|---|---|---|---|---|---|
| recIG – IDP | ||||||||
| Xembify® – CLL | ||||||||
| Immunology | Xembify® – Biweekly dosing - PID | |||||||
| Xembify® – Pre-filled syringes | ||||||||
| Gamunex® Bags | ||||||||
| Yimmugo® (IGIV NextGen) – IDP | ** | |||||||
| Albúmina 20% – Cirrhosis – PRECIOSA | ||||||||
| Hepatology / Intensive care |
Albúmina 5% – Acute on chronic liver disease – APACHE |
|||||||
| FlexBag® (U.S UE) | ||||||||
| Alfa-1 AT - in non-cystic fibrosis bronchiectasis |
||||||||
| Pulmonology | Alfa-1 AT 15% (SC) – AADT | |||||||
| Prolastin-C – AADT (SPARTA) | ||||||||
| Prolastin® vials 4-5g, (UE) | ** | |||||||
| Fibrinogen - Cong. deficiency & severe hypofibrinogen |
||||||||
| Hematology | Fibrinogen – Acquired deficiency | |||||||
| Fostamatinib1 – PTI – Refractory patients |
||||||||
| Yimmugo® (IGIV NextGen) PTI | ** | |||||||
| Infectious | GIGA 2339 – VHB | |||||||
| diseases | Trimodulin (IgM) – (EScCAPE) | |||||||
| GRF6019 – Alzheimer's | ||||||||
| GRF6021 – Parkinson's with dementia | ||||||||
| Neurology | Aβvac402 – Alzheimer's |
|||||||
| AKST4290 – Parkinson's | ||||||||
| GIGA564 – Anti-CTLA-4 mAb Oncology | ||||||||
| AKST4290 – Neovascular age-related macular degeneration (AMD |
||||||||
| Others | VISTASEAL™ (fibrin sealant) - Biosurgery pediatric use |
|||||||
| OSIG (Ocular Surface immunoglobulin) – Dry eye disease |
1 Association with Endpoint Health; 2 Rights licensed by Rigel Pharmaceuticals in la UE and other countries; 3 Project led by Araclon (Grifols investee) ** Commercialization initiated
Biotest projects
Clinical trial for subcutaneous immunoglobulin Xembify® to help prevent infections in patients with secondary immunodeficient chronic lymphocytic leukemia (CLL), which affects more than 375,000 people in the U.S. alone.
380+ participants 70 healthcare centers First patient treated in 2023 Conducted in the U.S. and Europe
SPARTA evaluates the efficacy and safety of two weekly intravenous alpha-1 dosing schedules in subjects with pulmonary emphysema caused by alpha-1 antitrypsin deficiency (AATD).
2 dosing regimens: 60 and 120 weekly/mg/kg Recruitment finalized in 2023 with 339 patients
Results expected in 2026-27
| 2024 | 2023 | 2022* | |
|---|---|---|---|
| Discovery | 19 | 24 | 19 |
| Preclinical | 32 | 23 | 28 |
| Clinical | 15 | 22 | 23 |
| Post-commercialization studies | 6 | 14 | 39 |
| Other projects | 10 | 16 | 14 |
| Total Biopharma R+D projects | 82 | 99 | 123 |
* Includes Biotest.
In 2024, Grifols continued to advance and support Biotest's R+D projects, which complement and enhance its innovation portfolio, expanding the availability of plasma-derived therapies in benefit of patients worldwide.
Phase 3 clinical study Adjusted Fibrinogen Replacement Strategy (AdFirst) in patients with elevated blood loss while undergoing spinal surgery or during abdominal surgery as a treatment for peritoneal pseudomyxoma (PMP).
A new polyclonal antibody preparation with a high content of immunoglobulins (IgM, IgA and IgG) to treat severe communityacquired pneumonia (sCAP).
Grifols continues to drive new knowledge of the plasma proteome through its investee Alkahest to determine plasma proteins associated with aging, a discovery that could extend its therapeutic benefit to other diseases, including those related to the central nervous system. At present, ongoing clinical programs are under way with plasma fractions and small molecules in patients with Alzheimer's disease, Parkinson's disease and neovascular age-related macular degeneration (AMD).
Grifols became an Araclon Biotech shareholder in 2012. Since then, it has supported and promoted its growth as a pioneering developer of projects to diagnose and treat Alzheimer's disease.
Positive results were reported in the phase 2 trial of ABvac40, an active vaccine against the Aβ40 peptide to treat patients with early-stage Alzheimer's disease (AD). Findings show ABvac40 had a favorable safety profile, stimulated a robust and enduring immune response against ASymbol 40, and showed some potential cognitive benefits in early-stage AD patients, meeting primary endpoints. While the trial was not designed to assess efficacy on neuropsychological scales and other disease markers, promising results were observed in some secondary exploratory endpoints between the ABvac40-treated group and placebo group.
In 2024, post-hoc analyses of the study demonstrated that the ABvac40 vaccine provided greater benefits for patients with amyloid deposits in the brain, with fewer cases of clinically significant decline on the MMSE scale compared to the placebo group. These benefits were particularly pronounced in the top 25% of patients, who exhibited a robust immune response to the vaccine.
The clinical data obtained were presented at various scientific conferences.
Further evidence was gathered on the potential mechanism of action of ABvac40, particularly its impact on the amyloid vascular pathology linked to cerebral amyloid angiopathy (CAA). A reassessment of MRI scans from the trial revealed a lower incidence of new cerebral microhemorrhages among patients treated with ABvac40 compared to those in the placebo group.
The manuscript highlighting the key results from the phase 2 clinical trial is currently under way, with publication in a prestigious journal expected in in 2025.
In addition to its ELISA ABtest-IA assays for analyzing Symbol -amyloid peptides in human plasma, which have shown potential in identifying cognitively normal individuals with brain changes associated with Alzheimer's disease, Araclon has also developed the ABtest-MS assay. This test enables the simultaneous determination of total Aβ40 and ASymbol 42 levels in plasma using liquid chromatography coupled with mass spectrometry.
In 2024, a significant portion of the data generated with ABtest-MS was presented to the scientific community. Also ongoing is the collaborative project with New York University's Grossman School of Medicine, focused on determining Aβ40 and Aβ42 levels in human plasma and studying their association with factors such as sleep and race. Collaboration also continues with the ADRC (Alzheimer's Disease Research Center) at NYU-Langone Hospital in the United States.
Progress was made in the use of amyloid markers to assist in the diagnosis of cerebral amyloid angiopathy (CAA) in collaboration with Vall d'Hebron Hospital (Barcelona). Also completed was the extension of the Clinical Validation Study for ABtest-MS in individuals with mild cognitive impairment (MCI). The study included more than 600 participants, who were grouped in two cohorts (Hospital Clínico San Carlos in Madrid and Santa María Hospital in Lleida).
A paper is expected to be published in 2025 presenting the results of a five-year longitudinal study on the FACEHBI cohort (ACE Foundation, Barcelona), as well as findings from the statistical analysis from the Clinical Validation Study. Additionally, results from other studies and collaborations are also anticipated for publication.
GigaGen is dedicated to the discovery and development of recombinant polyclonal antibody-based drugs to treat immunodeficiencies, infectious diseases and immunotherapy-resistant cancers. Its patented technology platforms enable the discovery of potent monoclonal antibody therapeutics and a new class of drugs: recombinant polyclonal antibodies.
Among other projects, GigaGen is working on the development of a recombinant IVIG (intravenous immunoglobulin) and a recombinant antithymocyte globulin (ATG) to treat transplant rejection and other inflammatory diseases.
In 2024, GigaGen dosed its first patient in a phase 1 clinical trial to assess the safety and tolerability of GIGA-2339, the company's first recombinant polyclonal antibody candidate for treating hepatitis B virus (HBV) infection, following its FDA clearance as an investigational new drug (IND).
GIGA-2339 includes more than 1,000 recombinant human antibodies targeting HBV to mimic the body's natural immune response, with the potential to eliminate the virus and activate the immune system. There is presently no cure for HBV, which affects more than 296 million people globally and causes over 800,000 deaths every year.
GigaGen dosed the first patient in its phase 1 clinical trial to evaluate its oncology candidate GIGA-564 for the treatment of advanced solid tumors. This marks the first oncology asset to enter clinical development.
The trial is being led by researchers at the U.S. National Cancer Institute (NCI) in close collaboration with the GigaGen team, as outlined in the cooperation agreement signed between the two organizations.
The new collaboration will finance the initial development of GigaGen's hyperimmune product targeting seven variants of botulinum neurotoxins A and B (BoNT), as well as a second, yet-to-be-identified biological threat. The grant amounts to USD 132.5 million over six years, covering product manufacturing and phase 1 trials for both programs. This partnership further underscores the Department of Defense's confidence in GigaGen technology and the company's capacity to develop vital therapies for highpriority pathogens.
Grifols also drives social progress by leading research and scientific advances in the diagnostics field. Its contributions and innovations in transfusion diagnostics for the screening and typing of blood, plasma and tissue donations are key to modern medicine, contributing to enhanced safety, quality and efficacy in blood transfusions and tissue donations.
Among their benefits, these innovations guarantee compatibility between donor and recipient, prevent disease transmission and optimize blood product inventories, enabling rapid and effective responses in critical situations. Grifols' technology has a significant positive impact on society by improving diagnoses and treatments in this area.
In 2024, Grifols continued to reinforce its industry leadership in transfusion safety:
Grifols' corporate environment and growth opportunities make digital innovation a central focus across the organization. Led by the Chief Digital Information Officer (CDIO), the company has made important inroads to explore, evaluate and enhance digital tools that add value to its business model.
Grifols advanced on its digital transformation in 2024, leveraging the experience and expertise acquired since 2018 to roll out a comprehensive redesign of its community and ecosystem grounded in a local approach with a global vision.
The company's digital strategy is built on three key pillars:
This comprehensive strategy fosters innovation from within and positions Grifols as a proactive player in adopting new ideas and industry practices. The company also promotes innovation through collaborations with external entities. One example is Grifols' partnership with Google to develop and implement the GIGA program (Grifols Innovation with Google Academy). Among its objectives, GIGA aims to drive experimentation with new digital technologies and promote cultural change within Grifols teams in relation to its digital innovation processes.
Another example is Grifols' 2023 incorporation in the Barcelona Health Hub (BHH), dedicated to promoting innovation and interaction in the digital health space. The BHH's 350 members include startups, healthcare institutions, universities, large corporations and investors. Through its involvement, Grifols explores and accelerates the adoption of cutting-edge digital health platforms and technologies.
| Commercial | Industrial | Plasma |
|---|---|---|
| Client | Value chain and | Donors |
| + value | operations | + experience |
| + optimization | + efficiency | |
| R+D | Quality | Corporate |
| New sources of value | + safety | + processes |
| + workforce |
experience

As a firm believer in the transformational impact and potential of artificial intelligence, Grifols is expanding AI-driven implementations to boost the efficiency and sustainability of its production processes, while harnessing its full capabilities in vital areas like R+D. Key AI projects in 2024 include:
A new OT-IT architecture enables data from Biopharma cooling plants in Barcelona to be read and written from the cloud, maintaining cybersecurity standards and data sovereignty. This architecture also facilitates real-time management of three cooling plants, optimizing energy performance and contributing to a 20% reduction in the energy consumed for climate control in the plants' clean rooms.
Grifols has implemented AI platforms in its Biopharma manufacturing plants to improve the performance of intravenous immunoglobulin (IVIg) production. The platform collects data from the production process, identifies critical parameters and learns how variation in those parameters affects the amount of protein obtained. Based on the information acquired, the platform proposes new thresholds with the objective of achieving higher IVIg yields.
Grifols continually works to optimize the efficiency and sustainability of its production processes in line with its growth strategy. Leveraging its in-house engineering expertise and collaborations with other institutions and organizations, the company explores various avenues to integrate new technologies and materials, automated systems and digitalization opportunities.
Its core projects in 2024 included the following:
New software was rolled out to manage devices used in Haema donation centers in order to improve efficiency, minimize errors and ensure compliance with Good Manufacturing Practices (GMP). The software's modular structure and scalability enable the management of both medical and non-medical equipment, including the documentation of digital master data, routine checks, recurring maintenance, phased qualifications, and instructions and records of device failures and repairs.
Wastewater with the highest organic load is segregated and sold as a by-product to a high-capacity biogas plant in Catalonia. There, the biogas is purified and converted into biomethane, which is subsequently injected into the natural gas distribution network. This process supports the circular economy by repurposing wastewater and contributing to the production of biomethane, a crucial element in decarbonizing thermal energy demand.
Grifols enhanced its GSF® (Grifols Sterile Filling) system, which has successfully protected products from contamination for over 30 years, by incorporating RABS (Restricted Access Barrier System) technology. This addition increases isolation through horizontal laminar flow and HEPAfiltered air at the aseptic filling point, and reinforces the protection of GSF® system's protection, which already minimized vial and cap exposure. Through this upgrade, the company reduces the risk of accidental contamination compared to other filling systems.
Founded by Grifols, Plasmatology was launched with the aim of becoming an industry reference in plasma-related research, from basic research to clinical applications. The journal has open access and indexed in a range of scientific databases.
9 articles published in 2024 42 articles published since its launch in 2021
Grifols' investigator-sponsored research (ISR) advances scientific knowledge of plasma proteins by supporting pre-clinical and clinical research.
EUR 7 M allocated to research over the past 5 years to complement public-sector investments
Grifols established the Grifols Chair for the Study of Cirrhosis in 2015 as a private, international chair under the European Foundation for the Study of Chronic Liver Failure (EF-Clif). The project is led by Professors Vicente Arroyo and Richard Moreau, president and managing director of EF-Clif, respectively. A Grifols representative serves on the foundation's executive board.
EUR 11.9 M invested over the last 5 years in liver disease research
These distinctions promote and showcase innovative proposals developed to enhance people's health, well-being and quality of life.
EUR 6.9 M allocated over the past 5 years to scientific awards and research grants
CONTENIDOS
| Governance of a listed company | 175 |
|---|---|
| Grifols' shareholder composition | 175 |
| Governance bodies | 176 |
| Sustainability governance | 180 |
| Performance and compensation | 181 |
| Business Conduct- ESRS G1 | 183 |
| Impacts, risks and opportunities | 183 |
| Ethics, integrity and human rights are at the heart of Grifols' corporate culture | 185 |
| Grifols Ethics Line and whistle-blower protection | 189 |
| Animal welfare | 190 |
| Political commitment and activities with advocacy groups | 191 |
| Management of relationships with suppliers | 192 |
| Alliance. associations and sponsorship | 195 |
| Cybersecurity and data protection | 196 |
| Impacts, risks and opportunities | 196 |
| Cybersecurity governance | 197 |
| Cybersecurity management | 197 |
| Data protection | 198 |
| Risk management and control | 199 |
| Governance Framework | 199 |
| Risk management | 201 |
| Main risks | 202 |
| Promoting a risk culture | 204 |
| Taxation | 205 |
| Grifols' aproach | 205 |
| Principles and good practices | 205 |
| Tax contribution | 207 |
| Grants | 208 |

Grifols made important advances in its commitment to creating long-term sustainable value, underpinned strong corporate governance and aligned with best practices.
The principles and best practices guiding Grifols' corporate governance ensure efficient, transparent and responsible management, fostering trust with investors and other key stakeholders.
Grifols is a publicly listed company with no extra-statutory or concerted actions among shareholders. Additionally, there are no restrictions– whether statutory, legislative or other types–on the transferability of securities or the right to vote.
Grifols S.A. share capital currently stands at EUR 119,603,705, represented by 687,554,908 shares which are fully subscribed and paid. The company's shares fall into two categories:
Grifols has two American Depositary Receipts (ADRs) programs in the United States: ADR Level I for Class A shares and ADR Level III for Class B shares. Level I ADRs are traded in U.S. dollars on the OTC markets, while Level III ADRs are listed in U.S. dollars on NASDAQ.

As a publicly listed company, Grifols has several channels to deliver clear, in-depth and timely information to its shareholders, including financial statements and sustainability reports. At the same time, it maintains regular contact with investors through roadshows, webinars and meetings. The company is dedicated to integrating sustainable and responsible practices in its operations and assessing its environmental and social impact.
Grifols is a publicly listed company in Spain and the United States, complying with all applicable legislation in both countries.
The General Shareholders' Meeting is Grifols' sovereign governing body. The company encourages all shareholders to attend, requiring no minimum share capital. Grifols' 2024 Ordinary General Shareholders' Meeting took place on June 14, with 55.95% of voting capital represented. Grifols' shareholders approved all the proposals submitted to a vote, except for the proposal concerning item 12 of the agenda (Authorization to the Board of Directors to call, if necessary, Extraordinary Shareholders' Meetings of the Company with at least 15 days in advance, in accordance with article 515 of the Capital Companies Act), as there was not sufficient quorum for its vote and approval.
The Board of Directors is Grifols' highest decision-making body. The Board is responsible for the company's management and legal representation and comprised by no fewer than three members and no more than fifteen, as stipulated in Article 20 of the Articles of Association and Article 7 of the Regulations of the Board of Directors. As of December 31, 2024, Grifols' Board of Directors was composed by 13 members.
Board members serve four-year terms, without prejudice to their indefinite re-election for subsequent terms of the same duration. The board has designated a lead independent director, although not being mandatory under Spanish legislation, and all committees are made up entirely by independent directors. This applies to the Appointments and Remuneration Committee, Appointments and Remunerations Committee and Sustainability Committee.
Grifols implemented several changes in 2024 to reinforce its governance, separating ownership and management spheres as outlined in its long-term corporate governance strategy, launched in 2022.
Following a successful transition period, the Chief Executive Officer was vested with all executive functions on 1 April 2024, bringing the company in line with best governance practices. As of September 2024, Grifols' chairperson holds a non-executive role, while Víctor Grifols continues to serve as Honorary Chairman after tendering his resignation as a board member on December 18, 2023.
Grifols publishes a Corporate Governance Report once a year. Approved by the Board of Directors, it provides detailed information on its ownership and management structures, among other relevant issues.

Board of directors 34 meetings
93.1% attendance
Audit Committee
14 meetings 100% attendance
10 meetings 96.7% attendance
5 meetings
100% attendance

VICTOR GRÍFOLS ROURA CHAIRMAN OF HONOUR

RAIMON GRÍFOLS ROURA PROPRIETARY DIRECTOR VICE-CHAIRMAN

TOMÁS DAGÁ GELABERT DIRECTOR OTHER EXTERNAL

MONTSERRAT MUÑOZ ABELLANA LEAD INDEPENDENT DIRECTOR AUDIT COMMITEE SUSTAINABILITY COMMITTEE
NON-EXECUTIVE CHAIRMAN

VÍCTOR GRÍFOLS DEU DIRECTOR PROPRIETARY

ANNE-CATHERINE BERNER DIRECTOR INDEPENDENT AUDIT COMMITTEE APPOINTMENTS AND REMUNERATION COMMITTEE SUSTAINABILITY COMMITTEE

ÍÑIGO SÁNCHEZ-ASIAÍN MARDONES DIRECTOR INDEPENDENT AUDIT COMMITTEE

NACHO ABIA CHIEF EXECUTIVE OFFICER

ALBERT GRIFOLS COMA-CROS DIRECTOR PROPRIETARY

ENRIQUETA FELIP FONT DIRECTOR INDEPENDENT APPOINTMENTS AND REMUNERATION COMMITTEE SUSTAINABILITY COMMITTEE

PASCAL RAVERY DIRECTOR INDEPENDENT
LAURA DE LA CRUZ GALÁN VICE-SECRETARY NON-MEMBER SECRETARY NON-MEMBER · AUDIT COMMITTEE

SUSANA GONZÁLEZ RODRÍGUEZ
DIRECTOR INDEPENDENT APPOINTMENTS AND REMUNERATION COMMITTEE

PAUL S, HERENDEEN DIRECTOR PROPRIETARY
NURIA MARTÍN BARNÉS
SECRETARY NON-MEMBER SECRETARY NON-MEMBER · APPOINTMENTS AND REMUNERATION COMMITTEE SECRETARY NON-MEMBER · SUSTAINABILITY COMMITTEE
Nacho Abia starts his new role as Grifols' new CEO on April 1, 2024, succeeding Thomas Glanzmann. In September 2024, he assumes full responsibility of the company's executive functions.
Víctor Grifols Roura was appointed Honorary Chairman in October 2023, although he no longer serves as member on the Board of Directors. The grandson of Grifols' founder, he played a pivotal role in the Company's transformation into a global industry leader and is regarded among the sector's most influential figures. He
Víctor Grifols Roura becomes
will continue to serve as an Honorary Chairman.
Honorary Chairman
On September 23, 2024, Grifols' Board of Directors announces its decision to name Thomas Glanzmann as a non-executive chairman to allow him to focus exclusively on his board responsibilities. This resolution is made following the successful completion of Nacho Abia's transition period, ensuring a smooth transfer of duties and knowledge without impacting the company's operations.
On November 27, 2024, Brookfield notified the CNMV (Spain's National Securities Market Commission) of its decision to terminate negotiations for an exclusion takeover bid of Grifols. Months earlier, on July 19, Grifols' Board of Directors signed a confidentiality agreement with Brookfield, granting the firm access to corporate information as part of its evaluation of a potential offer.
The possible transaction was first disclosed on July 7, 2024, when Brookfield and certain Grifols' significant shareholders sought the Board's approval to access information for a due diligence process and explore the possibility of a joint public takeover bid aimed at delisting the company.
experience in:
| 5 | > plasma industry | 38% |
|---|---|---|
| 7 | > healthcare | 54% |
| 1 | > medical science | 8% |
| 9 | > life tech and innovation | 69% |
| 7 | > financial and accounting | 54% |
| 3 | > risk management | 23% |
| 9 | > people and talent | 69% |
| 12 | > international business | 92% |
| 3 | > digital, AI, and Cyber | 23% |
| 3 | > innovation | 23% |
| 6 | > sustainability | 46% |
| 5 | > legal, regulation, and governance 46% | |
| 11 | > corporate strategy | 85% |
All independent directors have 4 or less other mandates
| 46% |
|---|
| 15% |
| 31% |
| 8% |
31% female board members 23% <50 years 31% between 50-60 years 46% +60 years
General Environment Social Governance Annexes Governance of a listed company
| Executive Team at the close of 2024 |
|---|
| RAHUL SRINIVASAN |
| CHIEF FINANCIAL OFFICER |
| JORDI BALSELLS VALLS |
| PRESIDENT PLASMA PROCUREMENT |
| DAVID BELL |
| CHIEF CORP AFF & LEGAL OFFICER |
| IGNACIO RAMAL SUBIRÀ |
| CHIEF INT, AUDIT & ENTERPRISE RISK MGMT |
| ANTONIO MARTÍNEZ MARTÍNEZ |
| PRESIDENT. DIAGNOSTIC |
| ROLAND WANDELER |
| PRESIDENT. BIOPHARMA |
| DANIEL FLETA COIT |
| CHIEF INDUSTRIAL SERVICES OFFICER |
| CAMILLE ALPI |
| CHIEF HUMAN RESOURCES & TALENT OFFICER |
| LLUIS PONS GÓMEZ |
| SVP. STRATEGY |
| JOERG SCHUETTRUMPF |
| CHIEF SCIENTIFIC INNOVATION OFFICER |
| JAIME GONZÁLEZ |
| CHIEF DIGITAL INFORMATION OFFICER |
| MARÍA TERESA RIONÉ LLANO |
| CHIEF COMMUNICATIONS OFFICER |
| ENRIQUE DE LA TORRE |
| CHIEF COMPLIANCE OFFICER |
| Ethics and compliance |
• Code of Conduct • Code of Ethics for Grifols Executives • Risk Control and Management Policy • Tax Compliance and Best Practices Policy • Crime Prevention Policy • Anti-Corruption Policy • Conflicts of interest policy • Policy on related-party transactions • Competition Policy • Clawback Policy • Policy and Procedure of the U.S. Open Payment Program • Grifols Ethics Line Policy |
|---|---|
| Workforce | • Diversity and Inclusion Policy • Policy on Director Diversity in the Composition of the Board of Directors • Remuneration Policy for Directors • Health and Safety Policy • Mental Health Policy |
| Human rights and social action |
• Human Rights Policy • Social Action and Community Investment Policy • Sustainability Policy • Plasma Donor Policy • Patient and patient organizations Policy • Animal Welfare Policy |
| Environment and climate change management |
• Sustainability Policy • Environmental Policy • Energy Policy • Climate Action Policy • Biodiversity Policy |
| Responsible communication |
• Internal Code of Conduct in Matters Relating to the Securities Market • Policy on Communication and Contacts with Stakeholders, Institutional Investors and Proxy Advisors |
| Privacy and security | • Global Privacy and Data Protection Policy • Cybersecurity Policy |
| Quality and supply chain |
• Quality Policy • Anti-falsification policy • Suppliers Code of Conduct • Plasma Donor Policy • Patient and Patient Organizations Policy • Global Procurement Policy |
*The coverage of the policies, codes and regulations in this table apply all Grifols group companies within the scope of consolidation.
Grifols has made important strides in recent years in integrating sustainability into its business model to amplify its positive impact and value creation. The company's commitment to sustainability is driven at the highest organizational levels and embedded into its corporate governance.
Grifols' Board of Directors formed a Sustainability Committee in 2020 to ensure compliance with its ESG-related principles and commitments, as well as consistency between its corporate culture and overarching purpose and values. Its oversight includes the preservation of stakeholder transparency policies such as financial and non-financial disclosures.
In general, relevant materials are first reviewed by the Sustainability Committee before they are shared with the Board of Directors. These include presentations on key sustainability policies that require approval or appraisal due to their direct impact on the organization; annual ESG reports; updates on global trends and new regulatory mandates; and strategic topics like double materiality. Information on Grifols' scores and rankings on sustainability indices and its market perception from an ESG perspective is also presented to the board.
This body of content allows the company to make informed and coherent decisions that accurately reflect its reality and environment. Information is shared with the CEO to ensure full consistency between Grifols' sustainability strategy and corporate objectives.
In 2024, an extraordinary meeting was held with Grifols' CEO on sustainability issues, while the Sustainability Committee held five formal meetings.
For its part, the Sustainability Steering Committee is a global, multidisciplinary team coordinated by the Investor Relations and Sustainability (IR&S) Department, whose vice-president reports to the Sustainability Committee.
Created in 2021, it meets at least once a year to promote ongoing dialogue to identify, establish, implement and ensure compliance with Grifols Master Plan objectives, and integrate and coordinate the reporting of non-financial and corporate sustainability information.
Under the auspices of the Sustainability Steering Committee, the IR&S Department leads training and engagement initiatives on ESG topics, as well as assesses global trends and Grifols' ESG strategy to bolster its standing as one of the world's most sustainable companies. More technical and detailed in nature, Steering Committee meetings serve as a bridge for all organizational areas involved in ESG matters.
Sustainability is a key priority in Grifols' corporate governance, which establishes mechanisms to ensure the compliance, coordination, implementation and review of organizational objectives. Through these efforts, Grifols strives to grow as a responsible, transparent company, dedicated to serving its diverse stakeholders.
| Approval | > | Board of Directors | ||
|---|---|---|---|---|
| Supervision | > | Sustainability Committee Audit Committee Appointments and Remuneration Committee |
||
| Follow-up | > | Sustainability Steering Committee | ||
| Implementation | > | Business Areas and Corporate Support Areas |
Independent member - Chairperson
Enriqueta Felip Font Independent member
Independent member
Secretary, non-member
Grifols' Sustainability Policy and 2021-2024 Sustainability Master Plan form part of its Strategic Plan and support the United Nations Sustainable Development Goals (SDGs). The development of a 2025-2027 plan is currently under way.
The Sustainability Policy is supported by other policies, programs and formal commitments to promote the material aspects of Grifols' activity from an ESG perspective.
Based on a materiality analysis, the Sustainability Master Plan outlines the 30 corporate objectives included in Grifols 2030 Agenda.
Grifols is dedicated to cultivating a performance-driven culture based on execution, efficiency, effectiveness and accountability. Reflecting this commitment, its short- and long-term incentive strategies incorporate sustainability performance in alignment with stakeholder interests.
Grifols' Long-Term Incentive Plan, approved by Grifols' 2023 Ordinary General Shareholders' meeting, is based on the concession of stock options to the approximately 220 employees in its leadership cadre.
In order to vest the options awarded, beneficiaries must have remained continuously employed by Grifols on each vesting date and meet the following conditions:
Beneficiaries who are not board members must attain a performance rating of 3 or more on a scale of 1 to 5, with 5 as the highest score. Assessments are carried out via the Grifols Performance System (GPS), a standardized tool to assess employee effectiveness and potential and provide relevant feedback.
Beneficiaries who serve on the Board of Directors must pass an annual evaluation led by the Appointments and Remuneration Committee.
Variable compensation for Grifols employees, including members of its governance bodies, is based on financial and non-financial metrics. Among other factors, it includes a specific metric tied to the achievement of environmental, social and corporate governance (ESG) objectives.
Of Grifols' total corporate objectives, 10% are linked to ESG factors, with 25% focused on environmental, 40% on social and 35% on governance criteria. Depending on whether the employee has only corporate objectives or additional ones related to their production plant, this percentage may be reduced from the total variable compensation.
metrics 90% financial metrics based on EBITDA
At the close of the 2024 fiscal year, the Chief Executive Officer's annual gross bonus target ranges from 0% to a maximum of 60% of his annual fixed salary, contingent upon achieving 100% of the objectives set by the Board.
If objectives are surpassed, his short-term variable compensation will increase proportionally to a maximum of 90% of his annual fixed salary. The percentage of variable compensation is based on the achievement of concrete annual objectives, which are quantitative and qualitative, specific, predetermined and measurable in line with standard practices of comparable companies. These objectives are consistent with Grifols' strategy, interests and long-term sustainability.
Annual objectives for both the Chairman and CEO are tied to financial and non-financial metrics and parameters approved by the Board of Directors upon the proposal of the Appointments and Remuneration Committee. In the 2024 fiscal year, these include:
For the 2025 fiscal year, CEO's annual objectives will be tied to financial and non-financial metrics and parameters, and approved by the Board of Directors upon the proposal of the Appointments and Remuneration Committee.
These will include financial, operational and business-related goals, as well as innovation-related criteria, in order to link their compensation with Grifols' financial performance, business progress and innovation pipeline. Non-financial objectives (ESG-related metrics) will also be considered, with specific objectives aligned with Grifols' sustainability strategy and 2030 Agenda.
The remuneration policy for members of Grifols' Board of Directors was last approved by the Ordinary General Shareholders' Meeting on June 16, 2023. The policy extends to the 2023, 2024 and 2025 fiscal years.
In 2024, the Appointments and Remuneration Committee conducted an in-depth review of this policy and the company's overall compensation system, taking into consideration the feedback received from shareholders, investors and other stakeholders, in addition to the results of the advisory votes on the annual remuneration reports presented at each General Shareholders' Meeting.
Since the date of approval, a series of events and circumstances prompted the Appointments and Remuneration Committee to recommend several modifications to the Remuneration Policy, which were subsequently approved by the General Shareholders' Meeting on June 14, 2024. These revisions include:
● Complete termination of the fixed remuneration previously received by Víctor Grifols Roura as Honorary Chairman, following his departure from the Board of Directors on December 18, 2023. As a result, he no longer qualifies for compensation.

Grifols' business conduct is defined by ethics, transparency, honesty, integrity, independence, regulatory compliance, human rights and a commitment to safety and quality.
| G1 BUSINESS CONDUCT |
||||
|---|---|---|---|---|
| Material IROs | Type | Description | ||
| CORPORATE CULTURE | ||||
| Ethical practices within the business model |
+ OO SP |
Integrity and respect for human rights are central to Grifols' culture and approach to managing its impacts, including environmental and ethical considerations arising from plasma collection from donors and the potential economic dependency this could create in vulnerable groups. |
||
| Perception of overall business performance |
R | Reputational damage due to poor market perception of the company's overall performance. | ||
| PROTECTION OF WHISTLE-BLOWERS | ||||
| Inefficient communication channels | - OO SP |
Ineffective communication channels for reporting incidents undermines employee trust and well being |
||
| ANIMAL WELFARE | ||||
| Risks to animal welfare | - R |
Risks to animal welfare associated with the use of laboratory animals. | ||
| POLITICAL ENGAGEMENT AND LOBBYING ACTIVITIES | ||||
| Open and transparent collaborations between public and private entities |
+ OO |
Increased open and transparent collaboration between public and private entities promotes alignment and ultimately facilitates achieving shared goals for societal development and well being. |
||
| MANAGEMENT OF RELATIONSHIP WITH SUPPLIERS INCLUDING PAYMENT PRACTICES | ||||
| Promoting ESG practices across the value chain |
+ SP |
Strengthening business resilience throughout the value chain via long-term relationships, applying codes of conduct and adopting sustainable practices to respect human rights, drive social development and enhance supplier performance. |
||
| New supply chain management regulations |
R | Stricter standards and emerging regulations on supply chain sustainability that require new investments and increased operational costs. |
||
| CORRUPTION AND BRIBERY | ||||
| Penalties and reputational damage from corruption and bribery incidents |
R | Cases of corruption or bribery within the value chain can generate unexpected supply disruptions, high legal costs and significant reputational damage to the company. |
||
| + Positive impact - Negative impact R Risk OO Own Operation SP Supply Chain |
Las siguientes políticas. acciones. Metrics and Targets permiten gestionar de una forma eficiente los principales IROs vinculados con la conducta empresarial,
| Material Sub-topics | Policies | Actions | Metrics and Targets |
|---|---|---|---|
| Corporate culture | • Code of Conduct • Code of Ethics for Grifols Executives • Quality Policy • Human Rights Policy • Risk Control and Management Policy • Crime Prevention Policy • Competition Policy • Board Remuneration Policy • Transparency Policy in the U.S. • Sustainability Policy • Internal Regulations on Conduct for Securities Market matters • Policy on Communication and Contacts with Stakeholders, Institutional Investors and Proxy Advisors • Tax Compliance and Best Practices Policy • Related Party Transactions Policy • Conflict of Interest Policy |
• Due diligence on human rights • Global compliance programs • New employees trained in the Code of Conduct • Annual staff training on the Code of Conduct • Annual employee signing of the Corporate Human Rights Policy |
Grifols Agenda 2030 targets • Maintain a Biopharma complaint ratio of ≤ 1/50,000* • Maintain fewer than 1 critical deficiency identified by external audits (regulatory health authorities) |
| Protection of whistle-blowers |
• Grifols Ethics Line Policy | • Grifols Ethics Line Program | |
| Animal welfare | • Animal Welfare Policy | ||
| Political influence and lobbying activities |
• Code of Conduct • Code of Ethics for Grifols Executives • Conflict of Interest Policy |
• No contributions to any political campaigns, parties or territories • Compliance with the U.S. Lobbying Disclosure Act (LDA) • Registration in the EU Transparency Register for Lobbies |
|
| Management of relationships with suppliers including payment practices |
• Supplier Code of Conduct • Global Procurement Policy • Conflict of Interest Policy |
• Modern Slavery and Supply Chain Transparency Statement (HR1) |
Grifols Agenda 2030 targets • Implement ESG criteria for suppliers covering 60–80% of total expenditure • ESG evaluation for 25% of total expenditure on suppliers |
| Corruption and bribery |
• Anti-Corruption Policy • Related Party Transactions Policy • Conflict of Interest Policy |
• Global Anti-Corruption Program • Training on corruption and bribery for at risk employees |
* Refers to the ratio of claims per unit of product distributed.
More information and details on these policies: Corporate Policies Grifols' website.
Grifols' corporate culture is firmly grounded in ethical principles that guide every aspect of the organization, including environmental initiatives. This commitment begins with an unwavering respect for human rights, which lies at the heart of its business conduct and corporate responsibility.
The company is dedicated to fostering an inclusive, diverse and equitable environment that upholds the dignity and well-being of its employees, collaborators, donors, patients and the communities in which it operates. The company evaluates its progress using tools such as surveys, audits and mechanisms, for instance the Grifols Ethics Line, for reporting inappropriate behavior to ensure its values are fully integrated and shared across the organization.
Grifols promotes a corporate culture centered on compliance. Through comprehensive compliance programs, the company ensures that all its activities adhere to legal regulations, international standards and industry best practices. Clear policies, ongoing training and rigorous auditing processes further reinforce Grifols' commitment to integrity and transparency.
The Grifols Code of Conduct and Code of Ethics for Grifols Executives establish the principles and guidelines that shape the organization, strengthening a culture of business ethics and compliance.
In 2024, the company introduced its manifesto on artificial intelligence (AI), committing to a human-centered approach focused on ethics, responsible use, sustainability and regulatory compliance in all AI applications within Grifols.
At Grifols, the Board of Directors and its committees play a critical role in promoting ethical business practices, ensuring alignment with human rights and maintaining compliance with applicable laws and best practices.
The Human Rights Policy, approved in 2022, is overseen by the Sustainability Committee, which ensures that Grifols' global operations uphold respect for human rights across the organization.
Additionally, the Anti-Corruption Compliance Program is supervised by the Board of Directors through the Audit Committee. This program includes initiatives to prevent corruption-related offenses, ensure adherence to anti-corruption laws and integrate ethical standards into all operations. The Criminal Risk Management System is also supervised by the Audit Committee, further reinforcing Grifols' commitment to ethical governance.
Respect for human dignity and individual rights is a core principle guiding Grifols' actions. The company's approach to research, development, production and marketing is rooted in the fundamental principles of bioethics, ensuring the safety and dignity of all individuals involved in its processes while addressing challenges posed by advances in health sciences.
Grifols adheres to various regulations, declarations and codes that underpin these principles, including the Universal Declaration of Human Rights (1948), the Declaration of Helsinki (1964), and the UNESCO Universal Declaration on Bioethics and Human Rights (2005).
Drawing on international reference frameworks such as the United Nations Global Compact, the UN Guiding Principles on Business and Human Rights, the OECD Guidelines for Multinational Enterprises and the ILO Declaration on Multinational Enterprises, Grifols has developed a global strategy to promote and ensure responsibility and commitment to human rights throughout its operations.
The 2030 Agenda for Sustainable Development and its Sustainable Development Goals (SDGs) recognize business activity, investment and innovation as key drivers of productivity, inclusive economic growth and job creation. Respect for human rights in business activities is integral to achieving many of these goals.
Between 2022 and 2024, Grifols has reinforced its human rights due diligence processes. This includes conducting a comprehensive analysis to address its responsibility to respect human rights, in line with the UN Guiding Principles on Business and Human Rights.
In 2023, Grifols published its Human Rights Due Diligence Report, covering the entire value chain. In 2024, the company further advanced its risk analysis of the value chain.
This due diligence and reporting process follows a human rights-based approach (HRBA) and aligns with UN and OECD guidelines. By integrating international standards into its strategies, Grifols adheres to the OECD due diligence phases and employs the Human Rights Impact Assessment (HRIA) method developed by the Danish Institute for Human Rights–a widely recognized approach for identifying actual and potential impacts on human rights.
Grifols integrates several principles of the United Nations Global Compact into its operations:

Principle 1. We support and respect the protection of internationally recognized fundamental human rights within our sphere of influence.
Principle 2. We ensure that we are not complicit in the violation of human rights.
Principle 10. We actively work against corruption in all its forms, including extortion and bribery.
For Grifols, compliance is more than a set of rules and procedures. It is a foundational way of understanding business activity that permeates all levels of the organization, promoting core values such as ethics, transparency and good corporate governance.
Grifols' compliance system not only protects the organization from legal sanctions but also serves as a catalyst for strengthening a corporate culture rooted in ethical values. At the same time, a strong corporate culture reinforces regulatory compliance by fostering an environment where employees act proactively and in alignment with the company's principles.
Grifols has implemented several compliance programs in different areas of its organization. Each program integrates policies, procedures and controls designed to ensure that the company's activities are conducted ethically, transparently and in compliance with applicable laws and regulations. The primary objective of these programs is to prevent, detect and address legal and regulatory risks across Grifols' global operations. These include:
Within the framework of its global compliance system, Grifols has established a Criminal Risk Prevention Model that applies to all its affiliates worldwide. This model is based on the Crime Prevention Policy, updated in 2024, which outlines the company's commitments to crime prevention and reflects Grifols' zero-tolerance stance toward any criminal act or unethical conduct. This zero-tolerance principle is articulated by the Board of Directors and formalized through the defined risk appetite for Ethics and Integrity.
The Criminal Risk Prevention Model is a cross-organizational component of the company's crime prevention strategy. It works in conjunction with various policies, procedures and controls that address specific areas, such as the anti-corruption program, the anti-competitive practices prevention program, the quality system and the environmental program. The primary objective of this model is to prevent, detect and if necessary, respond to risks related to criminal acts–particularly those that could result in corporate criminal liability, including breaches related to money laundering. This is achieved through the application of specific monitoring and control measures.
Grifols' Board of Directors oversees the development and implementation of the Criminal Risk Prevention Model. Responsibility for monitoring and supervising its operation and compliance has been delegated to the Audit Committee. To fulfill these responsibilities, the Audit Committee relies on the independent functions of Internal Audit and Enterprise Risk Management, which report to the Chief Internal Audit & Enterprise Risk Management Officer.
Each year, Internal Audit and Enterprise Risk Management assess the effectiveness of the Criminal Risk Prevention Model through internal and/ or external reviews. These reviews are designed to identify, analyze and evaluate criminal risks and associated control measures, ensuring that the controls are operating effectively or determining whether additional measures and/or remediation plans are necessary.
Although Grifols, S.A. and its Spanish affiliates are not subject to Spanish Act 10/2010 on the Prevention of Money Laundering and Terrorist Financing, and therefore are not bound by the formal and administrative obligations set by the law on certain groups, the company has proactively evaluated its exposure to these risks as part of its Criminal Risk Prevention Model, identifying the highest-risk activities and the key control mechanisms to mitigate these risks.
Grifols' Competition Policy prohibits all members from engaging in any behavior, whether by action or omission, that aims to, results in or could potentially result in the prevention, limitation, restriction, distortion or falsification of free market competition. Such actions are considered detrimental to the interests of competitors and more critically, to the interests of consumers and users.
Prohibited practices include collusive practices or agreements, such as market or supply allocation, collective boycotts, resale price fixing or the application of unequal commercial conditions, among others. Additionally, the abuse of a dominant position, such as denying production or supply, imposing predatory pricing or forcing the purchase of unrelated bundled products (tied or linked sales), among others, is prohibited.
In 2024, Grifols has not had any legal action or legal proceeding finalized, nor does it have any pending legal proceeding related to unfair competition or infringements in terms of monopolistic practices and against free competition in the markets in which it operates.
Grifols' Anti-Corruption Policy, aligned with the United Nations Convention Against Corruption, applies to all employees, regardless of their location, function or the affiliates to which they belong, as well as to third-party collaborators. The policy establishes standards for conduct and interactions with public officials, agencies and representatives of the public sector, as well as with private sector organizations and entities.
The company ensures compliance with this policy through various review processes and procedures under its Global Anti-Corruption Program.
Grifols enforces a zero-tolerance approach to bribery and corruption in an aim to maintain zero cases of corruption. The company does not tolerate any form of retaliation against individuals who, in good faith, report potential violations of applicable laws, rules and regulations or non-compliance with internal policies and procedures under the Anti-Corruption Program.
Grifols has established internal procedures that explicitly define acts considered as bribery and corruption, which includes a list of disciplinary actions, up to and including dismissal, applicable in the event of violations of its Anti-Corruption Policy.
In the absence of confirmed cases of corruption this year, the total amount of fines imposed is EUR 0.
Confirmed incidents of corruption in 2024: 0
Reviewed interactions between staff and public officials or other professionals in 2024: 4,839
To ensure adherence to anti-corruption policies and procedures, Grifols implements an annual training plan approved by the Chief Executive Officer and the Compliance Officer. This plan is tailored to address the specific training needs of affiliates, business units and employees, and adapted to their unique requirements.
Grifols conducts regular training sessions across all affiliates, designed to align with their specific activities and characteristics. Delivered either in person or online, these sessions include updates and reminders based on risk assessments, as well as refresher courses for existing employees and onboarding training for new employees. In addition, all employees have continuous access to compliance policies and procedures via the corporate intranet.
The duration of training varies depending on the content and the target audience. Management, directors and supervisory bodies receive specific training tailored to their responsibilities.
89% Percentage of employees trained on business ethics
| AMSB1 | At risk Managers | At risk functions | Other own workers |
|
|---|---|---|---|---|
| Training coverage | ||||
| Total employees | 19 | 1,524 | 10,221 | 9,523 |
| Total receiving training in the reporting year | 7 | 1,258 | 9,193 | 704 |
| Delivery method and duration | ||||
| Clasroom training (hours) | 1.6 | 1.6 | 1.6 | 1.6 |
| Computer-based training (hours) | 2 | 2 | 2 | 2 |
¹ Administrative, Management and Supervisory Bodies
| GRIFOLS | ||||
|---|---|---|---|---|
| -- | -- | -- | --------- | -- |
| AMSB1 | At risk Managers | At risk functions | Other own workers |
|
|---|---|---|---|---|
| Training coverage | ||||
| Total employees | 4 | 42 | 192 | 1,968 |
| Total receiving training in the reporting year | 3 | 42 | 155 | 1,832 |
| Delivery method and duration | ||||
| Clasroom training (hours) | 0 | 0 | 1 | NAP |
| Computer-based training (hours) | 2 | 0.67 | 0.67 | 0.67 |
¹ Administrative, Management and Supervisory Bodies
Compliance with the Anti-Corruption Policy is reinforced through a series of review processes tailored to the type of interaction. These reviews are guided by various internal procedures and supervised by the compliance function. Special attention is given to high-risk operations, including interactions with government officials, public bodies, healthcare professionals and healthcare organizations, where the analysis and management of potential conflicts of interest are prioritized. The review processes are designed to encompass the full scope of Grifols' market activities.
The Anti-Corruption Policy and Program are reviewed regularly by the internal audit function, which develops an annual audit plan based on a thorough risk analysis. In addition, external and independent audits are conducted to assess different aspects of Grifols' Global Anti-Corruption Program.
If a potential case of corruption is detected, the company promptly initiates an internal investigation, with the involvement of external legal advisors.
The Global Compliance Review Committee supports the Audit Committee of the Board of Directors in overseeing the Global Anti-Corruption Program.
The Board of Directors of Grifols, S.A. holds ultimate responsibility for ensuring compliance with the Anti-Corruption Policy and has delegated these oversight responsibilities to the Audit Committee.
Grifols' Global Anti-Corruption Program includes control mechanisms for third parties with whom the company intends to establish commercial or business relationships. Before initiating a commercial relationship, distributors, consultant, agents, brokers or other individuals or entities that are not part of Grifols and that are engaged or used by Grifols to:
(1) market, promote, sell and/or distribute Grifols' products; and/or
(2) provide services that enable or support the marketing, promotion, sale, distribution, reimbursement, registration, pricing and/or import-export of, or regulatory-related work for, Grifols' products and may involve any interactions with government officials undergo a thorough verification process comprising two phases: a first phase to ensure the legitimacy of the intended commercial relationship, and a second phase of due diligence, which includes an in-depth analysis of the third party, covering their organization, key employees, business practices, and reputation.
Contracts signed with third parties include anti-corruption obligations and an annex summarizing Grifols' Anti-Corruption Policy. Additionally, third parties are required to provide an annual certificate of compliance with the ethical standards outlined in the policy.
Certain third parties, such as international distributors, are also required to complete periodic online training on anti-corruption regulations, including the U.S. Foreign Corrupt Practices Act (FCPA).
Contracts include a clause granting Grifols the right to conduct audits, along with provisions allowing for the termination of business relationships in cases of non-compliance with anti-corruption laws, regulations and standards.
Grifols employees are responsible for continuously monitoring the daily activities of third parties under their management. The company's alert system for potential violations, coupled with an ongoing monitoring process, enables the swift identification, management and resolution of any warning signs.
The Grifols Ethics Line is a communication channel established by the company to enable employees and external stakeholders–including customers, suppliers, contractors, consultants, business partners and their employees–to raise concerns about ethical issues or report conduct that may constitute a violation of applicable laws, regulations or internal policies, including those related to human rights. Reports can be made anonymously, verbally or in writing, and all communications are treated with the utmost confidentiality.
Grifols' Ethics Line Policy underscores the company's commitment to upholding the highest standards of ethics and business conduct, fostering a culture where employees and external stakeholders feel comfortable raising questions or concerns about Grifols' conduct or practices without fear of retaliation.
The policy also outlines Grifols' approach to protecting whistle-blowers in order to support and encourage individuals to report concerns in good faith. It explicitly recognizes the risks of retaliation or victimization faced by whistle-blowers and commits to safeguarding their confidentiality and anonymity to the greatest extent possible, even if the reported concern or disclosure is ultimately unfounded. The policy further provides guidance on how to raise concerns and details the processes for reporting, investigation and remediation.
All allegations received are handled in accordance with established standard operating procedures to ensure thorough and adequate investigations, with corrective actions taken as necessary.
To ensure the proper functioning of this process, Grifols has appointed the Chief Internal Audit Officer as the person responsible for the Grifols Ethics Line (Global Ombudsperson). Additionally, where legally required, local communication channels have been established and designated individuals have been appointed to oversee them to ensure compliance with jurisdiction-specific requirements.
Subject to local requirements for each jurisdiction, the timeframe to conduct the investigation and to provide feedback to the whistleblower should not exceed 3 months from the acknowledgement of receipt. Although Grifols intends to promptly handle and investigate all questions and concerns received, recognizes that certain factors, such as the complexity of the issue reported, may require a longer period for completion, thus, in cases of exceptional complexity, this deadline may be extended for a maximum of an additional 3 months.
Grifols has a zero-tolerance policy for retaliation of any kind, including discrimination, against individuals who, in good faith, report violations of laws, regulations or internal policies and procedures, including the Code of Conduct and the Code of Ethics for Grifols Executives. Retaliation may result in disciplinary action, up to and including dismissal.
Retaliation is defined as any direct or indirect action or omission occurring in a work-related context that causes or may cause unjustified harm or damage to an employee as a result of a report. Protection against retaliation also extends to co-workers, family members, or any other individuals who assist the whistleblower, legal entities owned by the whistleblower and entities with which the whistleblower is employed or maintains a professional relationship. This protection also applies to all individuals specified under applicable laws.
Grifols promotes awareness of the Grifols Ethics Line across all its facilities, including plasma centers, by providing concrete information. Moreover, all Grifols employees are required to complete mandatory online training on the Grifols Ethics Line as part of the company's corporate training platform. Employees involved in case management also receive specialized training on the channel's operation and their responsibilities.
In 2024, Grifols received a total of 506 complaints through the Ethics Line, of which 199 were confirmed.
Out of 199 confirmed cases in 2024 (compared to 135 in 2023), 5 cases (5 in 2023) were identified as related to human rights violations, all of them linked to harassment within the organization. In all cases, the appropriate disciplinary measures were taken; verbal or written warning or suspension (4 cases), or coaching/training (1 case). Furthermore, during 2024, no allegations were received concerning corruption, money laundering, insider trading or customer data privacy.
| Number of complaints received |
Number of confirmed cases |
|||
|---|---|---|---|---|
| 2024 | 2023 | 2024 | 2023 | |
| Corruption or Bribery | 0 | 0 | 0 | 0 |
| Discrimination or Harassment |
27 | 97 | 10 | 33 |
| Customer Privacy Data | 0 | 0 | 0 | 0 |
| Conflicts of Interest | 1 | 9 | 1 | 7 |
| Money Laundering or Insider Trading |
0 | 0 | 0 | 0 |
| Environment, Health and Safety |
12 | 7 | 2 | 2 |
| Manufacturing / R&D / Patient and Donor Safety |
4 | 6 | 2 | 4 |
| Employee Relations | 368 | 160 | 176 | 76 |
| Others | 94 | 84 | 8 | 13 |
| Total | 506 | 363 | 199 | 135 |
*In 2024, the reportable events catalog was updated as part of the Grifols Ethics Line review and update project initiated in 2023, following the approval of the new policy. To facilitate data comparison, cases received and confirmed during 2023 have been reclassified according to the new catalog categories.
Grifols recognizes the intrinsic value of animals and respects society's ethical concerns regarding their use in research. Grifols' Animal Welfare Policy sets out welfare requirements based on the principle that animals should always be treated as living creatures, ensuring their use for research purposes is limited to areas that ultimately benefit human health.
When the use of animals is necessary to support the efficacy, safety or quality testing of Grifols' products or research programs, the company complies with and often exceeds mandatory regulations. Additionally, Grifols applies the principles of the 3Rs to ensure a high level of animal welfare:
In line with the Animal Welfare Policy, Grifols commits to:
Grifols does not contribute to any political campaigns or political parties anywhere in the world.
Advocacy is a legitimate activity and a fundamental part of the democratic process, allowing people to share their viewpoints and concerns with public officials. For Grifols, it entails interacting with and educating political leaders on the importance of plasma-derived medicines and the need for patients to have unrestricted access in healthcare centers.
The company's Code of Conduct and Anti-Corruption Policy establish guidelines and the appropriate standards of interaction between Grifols employees and public officials.
Grifols is committed to complying with the highest ethical standards in its dealings with public officials, including the obligation to act with the utmost integrity and transparency. In the U.S., Grifols complies with all federal, state and local regulations, regularly submitting transparency reports to the U.S. Congress as mandated by the Lobbying Disclosure Act (LDA). These reports outline the company's lobbying-related expenses, encompassing direct costs for external consulting services and a proportional allocation of Grifols employee salaries based on the time dedicated to performing these activities. These expenses do not include political donations, as Grifols does not contribute to political campaigns in the United States.
Grifols' lobbying disclosure reporting requirements are governed by standard operating procedures that cover its activities in the United States and European Union. The company does not make campaign contributions to political candidates or government officials, either directly or indirectly.
Grifols has formed part of the European Union's Lobby Transparency Register since 2019, adhering to the rules of conduct governing relations with EU institutions as articulated in its code of conduct. Through this register, the company is authorized to interact with EU institutions and communicate its activity and positions on EU policies. Grifols also takes an active role in public consultations related to health and industrial policies.
The company is also a member of three organizations that are listed in the European Union's registry: Plasma Protein Therapeutics Association (PPTA), European Confederation of Pharmaceutical Entrepreneurs (EUCOPE) and MedTech Europe.
Grifols focused part of its efforts in 2024 on advocating for legislative changes in the U.S. Congress to increase patient access to plasma-derived medicines. Specifically, the company lobbied for modifications to the Medicare Part D program. At the same time, the company collaborated with patient organizations to support key legislative initiatives aimed at improving reimbursements and treatment options for patients with rare and orphan diseases in diverse care settings, including home care and specialized treatment centers
Grifols participates in health policy debates with a broad network of EU stakeholders to help improve people's access to health care. In 2024, the company closely monitored core healthcare policies and engaged with the key stakeholders and policymakers involved, sharing its expertise and vision to help improve the regulatory environment for plasma-derived products.
| 2024 | 2023 | 2022 | |
|---|---|---|---|
| Lobbying expenditures in the U.S. as reported under the LDA | USD 1,450,000** | USD 1,080,000 | USD 815,000 |
| Estimated annual costs related to activities covered by the European | |||
| Transparency Register | EUR 50,000 – 99,000 | EUR 50,000 – 99,000 | EUR 100,000 |
* U.S. data includes contributions at both federal and state levels. These figures do not include any contributions to public campaigns, as Grifols does not contribute to political campaigns in the United States.
** 2024 estimate.
In 2023, the European Commission released a proposal to update general pharmaceutical legislation, which must follow its applicable legislative process in the Parliament and Council of the European Union. Grifols collaborates with different institutions and stakeholders to guarantee the proposal advances access to healthcare, promotes R&D investments in the European pharmaceutical space, and recognizes the unique nature and qualities of plasma-derived medicines.
On July 17, 2024, the Official Journal of the European Union published Regulation (EU) 2024/1938 of the European Parliament and the Council, dated June 13, 2024, on quality and safety standards for substances of human origin (SoHO) intended for human use. Member States of the European Union have until 2027 to fully implement this directive.
This regulation repeals Directives 2002/98/EC and 2004/23/EC, which established quality and safety standards for the donation, procurement, testing, processing, preservation, storage and distribution of cells and tissues.
Created in January 2024, the Critical Medicines Alliance (CMA) is an advisory body that brings together relevant stakeholders from EU Member States, key industries, civil society and the scientific community. Since most plasma-derived medicines are considered critical, Grifols participates in CMA discussions to identify supply-chain vulnerabilities.
Grifols enhances business resilience in its value chain through long-term relationships; adherence to codes of conduct, including the Supplier Code of Conduct, which suppliers must follow; and the promotion of sustainable practices that respect human rights, advance social progress and optimize supplier performance.
As part of this commitment, Grifols introduced a new supplier preonboarding questionnaire in 2023 to assess different aspects related to ESG (environmental, social and governance) criteria. The questionnaire is scheduled to be updated in 2025 to align it with the latest regulations and trends in value chain due diligence.
Grifols is working actively to implement new procedures, analytical tools, data control systems, and supplier management practices to expand its knowledge and gain greater control over its supply chain, in addition to enhancing its supplier evaluation and due diligence processes.
In parallel, the company is incorporating improvements in response to recent regulatory developments, such as the requirements outlined in the Corporate Sustainability Due Diligence Directive (CSDDD). Through this proactive approach, Grifols is able to stay ahead of regulations and adopt industry best practices, reinforcing its commitment to sustainability and operational excellence.
In 2024, Grifols conducted its first analysis to identify and assess ESG (environmental, social and governance) risks in its supply chain. This analysis was structured into three main phases.
This process is enabling Grifols to significantly enhance its ESG risk identification procedures, while developing a broad range of effective mitigation and remediation measures to address the risks identified across its value chain.
In 2024, Grifols hired an external consulting firm to assess the integration of ESG criteria into its Global Procurement system, as well as to design a new global ESG procurement framework, expected to launch in 2025. It includes several key initiatives including the implementation of a technological solution to identify, monitor and classify supplier ESG risks based on the identified risk levels. In addition, the tool will also enable the collection of specific supplier information and data.
In addition, the company will update its master service agreement (MSA) used with its suppliers to include specific clauses addressing ESG factors and develop internal training programs, scheduled for implementation in 2025, to strengthen ESG competencies within the organization.
These initiatives aspire to mitigate risks, as well as to support and guide suppliers with lower maturity in critical areas such as respect for human rights and the importance of reducing emissions.
Recognizing that corporate responsibility extends beyond direct actions and in line with new challenges associated with the value chain, Grifols' Global Procurement department has, since 2024, dedicated two individuals exclusively to managing risks and ESG criteria within its value chain.
Grifols requires all of its suppliers to comply with the applicable legislation in their countries of operation. It further reinforces this requisite with a Supplier Code of Conduct, which defines the minimum standards of ethical, social and environmental behavior that suppliers must adhere to.
Framed from an ethical standpoint, the Code regulates conflicts of interest, fair competition, commercial controls, the fight against bribery, corruption measures, the acceptance of gifts, money laundering, product quality and safety, clinical trials and animal welfare, among others.
In the areas of labor and human rights, it emphasizes respect for human rights and the promotion of fair treatment, and prohibits practices such as forced labor, modern slavery and child labor. The code also includes concrete guidelines on health and safety, environmental management and the development of sustainable management systems, ensuring responsible operations throughout the entire value chain.
Grifols' Global Procurement Policy outlines the guidelines and common procedures for purchasing processes and supply strategies, ensuring that goods and services are procured through transparent, objective, timely, ethical and cost-effective decision-making.
This policy establishes a consistent, unified framework for procurement processes across the entire organization, supporting more efficient risk management and ensuring total compliance with all internal and external policies, procedures and regulatory controls.
Specifically, this policy includes criteria related to ethical, social, environmental and privacy standards aligned with health, safety and environmental policies. In addition, it promotes sustainable procurement principles within purchasing processes and ensures maximum transparency in supplier relationships, embedding the values outlined and supported by Grifols' Human Rights Policy and Sustainability Policy.
Ethical compliance and respect for human rights are among its fundamental pillars. To this end, all professionals involved in the process, whether Grifols employees or external suppliers, must adhere to the following principles throughout: compliance with laws and regulations; integrity, impartiality and fairness; transparency, confidentiality; and due diligence, among others. In addition, the policy promotes the integration of requirements, specifications and criteria compatible with environmental and societal protection into procurement processes.
Grifols' Supplier Qualification Management System assures all raw materials undergo rigorous and continuous evaluation processes, including plasma from external suppliers and critical non-plasma suppliers.
Grifols has a robust system of routine supplier audits to guarantee compliance with GMP (good manufacturing practices) regulations and quality standards in all of its business units.
Global Procurement promotes long-term relationships, guarantees compliance with ethical standards via a Corporate Procurement Policy, and ensures the application of regular supplier evaluations and performance metrics. It is also responsible for analyzing active suppliers to determine which are significant and consequently subject to greater ESG scrutiny. In carrying out this classification, Grifols bases its analysis on the category and the annual spend generated with each supplier.
In 2024, 43% of suppliers by spend (volume) were evaluated under ESG criteria.

*Significant suppliers: suppliers identified as having substantial risks of negative ESG impacts, significant business relevance to the company or a combination thereof. Critical suppliers essential for the business are also included, although in most cases, these are only evaluated for their business relevance.
* Tier 1 suppliers: suppliers that directly supply goods, materials or services (including intellectual property (IP) and patents) to the company. If not specified, suppliers are assumed to be Tier 1.
More details in "Social" chapter, "Patients and healthcare professionals" ESRS S-4.
Grifols' payment practices are designed to ensure clear, efficient processes that are aligned with its internal policies. They apply to both external suppliers and intercompany transactions, taking into account the specific needs of each type of supplier. Two main policies oversee Grifols' payment practices:
By regions, payments are made as follows:
Grifols has several practices in place to make sure small- and mediumsized enterprises (SMEs) are paid on a timely and predictable basis, reinforcing their financial stability and relationship with the company. These include reduced payment terms (30 to 60 days); prior approval by the Treasury Department; partial advances for specific projects or deliveries; supply chain finance; prioritization in payment schedules and fixed payment dates (e.g., the 15th or 25th of the month) to help SMEs manage their liquidity; process digitalization to reduce payment and approval delays; and transparent communication to quickly resolve issues.
In 2024, the global the average payment period for suppliers was 51 days, compared to 71.60 days in 2023.
As of December 31, 2024, Grifols has no pending legal processes related to late payments to suppliers.
Grifols' alliances and partnerships are focused on strategic sectors such as the plasma industry, pharmaceuticals, medical technology, and biotechnology. The company's commitment is demonstrated through its support for key projects, advocacy for industry policies, and promotion of innovation. Grifols ensures that all initiatives align with high ethical and safety standards, ultimately benefiting both patients and the broader healthcare community.
Although not a material aspect for the company, Grifols is an official sponsor of UEFA Women's Football from the 2021/22 season until 2025, under a four-year agreement.
This sponsorship includes competitions such as the UEFA Women's Champions League, the UEFA Women's Euro and other women's tournaments. Grifols chose to support UEFA women's football as part of its commitment to gender equality and the development of a fairer and more sustainable future. The company believes that sport is a powerful platform for promoting equality, helping to develop skills and values that inspire young girls and empower women in the workplace and in society. The total sponsorship amount is EUR 3.12 M.
| Activity | Involvement / commitment | 2024 contribution |
|---|---|---|
| Plasma industry | Grifols supports various projects related to the plasma industry, including the joint promotion of a global code of conduct, educational campaigns, access to clinical treatments, procurement of plasma as a raw material, and awareness campaigns on rare diseases. |
EUR 2,097,163 |
| Pharmaceutical industry |
Defense of policies and practices to promote the discovery of and access to life-enhancing medicines and vaccines for people around the world. Efforts to reinforce regulatory systems to ensure maximum safety throughout the value chain, from production to patient administration while acting ethically and professionally in alignment with Grifols Codes of Conduct. |
EUR 238,596 |
| Med-tech industry | Efforts to highlight the social value and contribution of medical technologies, facilitating their access to patients, healthcare professionals, operators and healthcare systems. Promotion of valuebased innovation to create more sustainable healthcare systems and meet the growing needs and expectations of health and medical-care systems. Adherence to the highest ethical standards for all training initiatives and interactions with healthcare professionals. |
EUR 127,610 |
| Biotechnology industry |
Participation in national non-profit associations of several bio-tech firms, aimed at increasing their social awareness and promoting innovation by advocating for public policies that favor the growth of this essential industry. |
EUR 77,787 |
Ethics, transparency, honesty, integrity, independence, legal compliance, respect for human rights, safety and quality are the cornerstones of Grifols business conduct.
| Material IROs | Type | Description |
|---|---|---|
| CIBERSEGURIDAD | ||
| Risk of data leaks due to the increase in cyberattacks |
- OO |
Information security risks have been on the rise in recent years as a result of cyberattacks and data breaches perpetrated by cybercriminals. To address this risk, Grifols has implemented a series of cybersecurity measures to help protect the personal data of everyone involved in its activity and operations. |
| Interruption of operations due to cyberattacks + Positive impact - Negative impact R Risk OO Own Operation SP Supply Chain |
R | Cyberattacks and cybersecurity failures that can lead to stoppages and disruptions during the manufacturing process. |
The following policies, actions, metrics and targets allow Grifols to efficiently manage its main cybersecurity-related IROs.
| Material Sub-topics | Policies | Actions | Metrics and Targets |
|---|---|---|---|
| • Cybersecurity Policy • Global Privacy and Data Protection Policy |
• Employee training on cybersecurity • Incident management procedure • Procedure related to personal data incidents |
||
| Cybersecurity and data protection |
• Training for all employees, with concrete actions for those who routinely process personal data • Available by processing and/or group • Explanation of how and why Grifols uses personal data for different purposes |
The Audit Committee on Grifols' Board of Directors is responsible for supervising and evaluating the efficiency of the company's cybersecurity management and control measures. The Committee is supported by the Internal Audit and Corporate Risk Management Division, whose director provides updates at least twice a year on cybersecurity control and management issues.
Grifols' chief cybersecurity governance and commitments are outlined in the Cybersecurity Policy, approved by the Board of Directors in 2023.
The head of the Information Security Office (ISEC), reporting to the Chief Digital Information Officer, is charged with developing and implementing Grifols' cybersecurity policies, standards and procedures, as well as supervising the roll-out and effectiveness of its information security management system.
Grifols has the necessary resources to ensure a cyberenvironment supportive of its business priorities while complying with established cybersecurity objectives.
All of Grifols' cybersecurity initiatives align with the international framework of the U.S. National Institute of Standards and Technology (NIST) and ISO27001.
In 2024, Grifols recorded no relevant cyberattacks, cyber-related thefts, loss of sensitive data nor damage to physical assets that affected the normal course of its operations.
Grifols' information security strategy is founded on a risk-based approach and implemented through the requisite procedures and tools to ensure that cybersecurity risks are appropriately identified, monitored and managed.
The ISEC identifies the security initiatives and projects that should be implemented to achieve the company's approved risk levels. These initiatives are outlined in the Security Master Plan, which is updated on a regular basis.
Grifols' Security Operations Center (SOC) runs 24 hours a day, seven days a week, offering comprehensive coverage for security events across its data centers, perimeters and workstations.
These services are activated upon receiving alerts from the security information and event management (SIEM) system, as defined by the Information Security Office. Grifols' cyber-intelligence capabilities provide information on threat actors and their techniques and tools, allowing for the swift deployment of controls to prevent the success of cyberattacks.
The incident response team intervenes when events detected by the SOC are likely to become security incidents. The team uses digital forensic analysis and incident response (DFIR) capabilities to analyze, contain and mitigate their risk, as well as prevent their recurrence. Grifols conducts regular tests to evaluate the response and recovery capabilities of tools, procedures and equipment.
Grifols has an annual training and cybercommunication plan to bolster its information security management system and promote organization-wide awareness. This plan is updated to reflect new threats and the specific needs of Grifols' business areas. Training sessions are mandatory and include phishing simulation exercises, among others, totest employees' knowledge.
In 2024, 78,24% of users registered in the Grifols Training Platform (GTP) completed global cybersecurity training.
The company's security certifications include ISO27001 and the National Security Scheme (ENS) for certain activities and group companies.
In 2024, Grifols conducted a thorough evaluation of its cybersecurity systems to assess the company's strengths and weaknesses relative to industry standards, identify potential vulnerabilities and uncover areas for improvement. Simulated threat scenarios were carried out as part of this process, giving the organization valuable insights into its detection, protection and response capabilities.
The evaluation's findings enabled the company to design a clear roadmap of actions to reinforce its cybersecurity against current and future risks, ensuring operational resilience and the protection of critical data. Key areas of focus include:
The company complies with all applicable data-protection laws and regulations and works with suppliers that provide adequate guarantees and privacy measures. The Global Privacy and Data Protection Policy, mandatory for all employees, establishes a robust framework for the processing of personal data, as well as outlines all pertinent data protection and security principles.
All employees receive training on the Global Privacy and Data Protection Policy as training and awareness are critical to protecting privacy. Additional training is also imparted to team members who process personal data as part of their regular job functions.
In 2024, Grifols ensured that all employees whose roles include the processing of personal data had access to privacy training and awareness sessions. Specifically, more than 70% of these employees actually accessed these initiatives, including training on the necessary steps to take in the event of a security incident that could lead to a data security breach.
Grifols has in place rigorous technical and organizational security measures to safeguard its organizational assets and users in a cyber-environment, as well as to protect the confidentiality of stakeholders' personal data.
The Risk Control and Management Policy enhances confidence in Grifols' ability to achieve objectives and strategic goals, reassuring patients, donors, employees, shareholders, customers, vendors and other stakeholders by anticipating, controlling and managing the risks to which Grifols is exposed.
It establishes the basic principles, roles and responsibilities, and general framework for managing and governing risks, including sustainability risks and controls.
This policy is implemented through a comprehensive risk control and management system based on COSO (Committee of Sponsoring Organizations of the Treadway Commission) principles, which include governance and culture, strategy and objective-setting, performance, review and revision, information, communication and reporting.
The main features of Grifols' risk control and management governance system and the process used to identify, evaluate and manage significant risks are outlined in the following section.
The company has a clear organizational risk-governance framework, delineating risk-management responsibilities across all hierarchical levels.
The Board of Directors approves the Risk Control and Management Policy, delegating the Audit Committee to oversee the effectiveness of the risk control and management system. The Board of Directors is also responsible for determining the company's risk appetite, defined as the nature and extent of risks that the company is willing to assume to achieve strategic objectives.

The Audit Committee, comprised exclusively of independent board members, oversees the effectiveness of Grifols' risk management and internal control systems, both financial and non-financial. In this role, it ensures the main risks, including any operational, technological, cybersecurity, legal, social, environmental, political, reputational or corruption related risks, are adequately identified, managed and communicated.
Additionally, the company established a Corporate Risk Committee in 2020 to ensure proper oversight of the assessment, management and monitoring of risks, as well as the integration of risk management into business processes. In 2024, Grifols implemented changes to create a more agile governance structure, streamlining the risk management process by discontinuing the Corporate Risk Committee and assigning its responsibilities to the CEO for day-to-day operations and, when required, to the Executive Committee.
The Enterprise Risk Management (ERM) function supports the Audit Committee in overseeing the effectiveness of Grifols' risk control and management system. The ERM function operates independently of senior management and is responsible for promoting, supporting, coordinating and verifying the application of the Risk Control and Management Policy. In alignment with other risk management initiatives, particularly those led by Sustainability, the ERM function assists the Audit Committee, CEO and Executive Committee in executing day-to-day activities related to the implementation of the risk management infrastructure, framework, approach, risk assessment, continuous monitoring and reporting processes.
Both the Board of Directors and the Audit Committee meet periodically with those responsible for managing the company's main risks, including the heads of Grifols business areas and assurance functions, in addition to external legal advisors and auditors. In 2024, the topics of discussion included cybersecurity, compliance, finance, and sustainability, among others.
The Audit Committee's oversight also includes guaranteeing the independence of Grifols' internal audit function, ensuring it has sufficient resources and budget; presentations to the Board of Directors to approve or propose the Internal Audit function's work orientation and annual work plan, ensuring that its main focus is on relevant risks; receive periodic
As part of Grifols' risk control and management system, the company developed a risk appetite framework to define acceptable levels of risk in alignment with its business objectives and market context.
information on its activities; and verifying that top management takes into account the conclusions and recommendations of its reports.
Additionally, the Sustainability Committee, acting under the auspices of the Board of Directors, is responsible for overseeing and ensuring adherence to the Sustainability Policy and managing the associated risks.
Management's responsibility for achieving organizational objectives includes both first- and second-line roles:
The Third Line, represented by the Internal Audit function, operates independently from management, reporting directly to the Board of Directors through the Audit Committee. This independence ensures that Internal Audit can provide independent and objective assurance and advice on the adequacy and effectiveness of governance and risk management, promoting the achievement of corporate objectives and continuous improvement. Additionally, Internal Audit communicates significant internal control deficiencies and proposed mitigation plans to senior management and the Audit Committee, ensuring that any issues are addressed promptly and effectively to maintain robust risk management.
In 2024, as part of its annual plan activities, the Internal Audit function conducted an assessment of the current maturity of core ERM activities. Indentify risks
General Environment Social Governance Annexes
Grifols has a comprehensive and continuous risk control and management process to identify, evaluate and manage all relevant risks that Grifols faces or may face, as well as assure that risk considerations are integrated throughout the company.
This process applies to Grifols, S.A. and its subsidiaries, encompassing all risk categories defined in the Risk Control and Management Policy. It comprises the following recurring activities:

Grifols reviews its risk exposure on a regular basis. Risk owners and assurance functions continuously identify risks to which the company is exposed in the ordinary course of its activities that could affect the achievement of its objectives. ERM utilizes these risk identification results to identify risks on an enterprise level. This process is supplemented with quarterly risk scans conducted by ERM to identify internal and external trends. These risk scans involve extensive analysis of external information sources, one-on-one discussions with management team members, senior executives, assurance functions and other employees, as well as monitoring the main risks ("top risks") identified in the previous year based on the evolution of selected risk indicators. This process ensures thorough and continuously updated risk identification, incorporating insights from key internal stakeholders and various information sources, including climate change risk evaluations.
In addition to assessing current and evolving risks, ERM evaluates emerging risks that could impact the company's ability to achieve its long-term objectives over a three- to five-year horizon. These emerging risks and their potential effect on the company are further analyzed to determine if they should be prioritized as top risks.
The identified risks are classified according to the risk taxonomy defined in the Risk Control and Management Policy and evaluated in terms of impact and likelihood of occurrence. To prioritize the risks, ERM completes risk scoring considering the risks' speed and interdependencies. The updated list of top risks proposed by ERM is submitted for review and approval by the Executive Committee, which prioritizes those risks requiring immediate response and/or increased oversight. The list is subsequently presented to the Audit Committee and/or the Board of Directors, providing the basis for the risk management priorities for the following year.
Based on the risk assessment results, management evaluates the appropriate responses and prioritizes mitigation efforts. By considering the prioritization assessment and weighing the benefits against the costs, risk owners determine the necessary measures and internal control procedures to prevent, avoid or minimize risks.
For top risks, ERM identifies and evaluates the existing controls to ensure that risk remains at an acceptable level within the defined risk appetite. If the residual risk exceeds the defined risk appetite, the risk owners must develop a risk mitigation plan. This plan must be validated by ERM and the corresponding assurance function. The Executive Committee receives regular status updates on the progress made in implementing these mitigation plans.
Risk owners and assurance functions continuously monitor risks to identify changes in the external and internal environment that might increase the impact or likelihood of a risk beyond acceptable levels, as defined by the risk appetite framework. For "top risks", ERM monitors changes in risk exposure using key risk indicators, with reporting thresholds aligned to the established risk appetites.
ERM periodically submits reports on "top risks" to the CEO, Executive Committee and Audit Committee throughout the year. These include details on existing control measures, planned risk mitigation actions, risk factors and emerging risks. This process facilitates dynamic and agile discussions on risk management strategies and oversight.
The table below outlines Grifols' main risks ("top risks") for 2025, which remain largely unchanged from those identified for 2024. Other ESGrelated risks, not all at the level of top risks, are disclosed in detail in their specific chapters.
The full description of Grifols' risks is publicly available in the 20F report, which is updated every year.
| Risk | Assessment and Mitigation Activities | |
|---|---|---|
| Cybersecurity | Information security risks have been on the rise in recent years due to an increase of cyber-attacks and data breaches perpetrated by cybercriminals, insiders or affected third parties, leading to business interruptions and the exposure of sensitive data. |
|
| To this end, the company has implemented a comprehensive information security management system. Aligned with international standards and best practices, it establishes clear objectives, roles and responsibilities, as well as policies and procedures to: (i) identify and assess cybersecurity threats; (ii) protect critical assets; (iii) detect and respond to cybersecurity threats; and (iv) recover business processes affected by a cybersecurity incident. |
||
| See chapter Cybersecurity and data protection for more information | ||
| Financial Leverage Ratio | A high level of indebtedness could have significant adverse effects on Grifols' business, making the company more vulnerable to economic downturns and restricting its ability to make strategic acquisitions or exploit other business opportunities (among other impacts). |
|
| In 2024, Grifols executed several transactions to advance its balance sheet improvement process in line with its key priorities of enhancing cash flow generation and proactively and prudently managing debt maturities and levels. |
||
| Research and Development of Products |
Research and development represents a significant aspect of Grifols' business, whose core R&D objectives are to (i) discover and develop new products, (ii) research new applications for existing products and (iii) improve manufacturing processes to improve yields, safety and efficiency. |
|
| The company faces various obstacles to successfully translate these efforts into profitable products, including, but not limited to, the successful development of an experimental product for use in clinical trials; the design of clinical study protocols acceptable to the FDA and other regulatory agencies; the successful outcome of clinical trials or its ability to scale its manufacturing processes to produce commercial quantities. |
||
| Despite this, in 2024 the company achieved innovation milestones and set the course for long-term success by accelerating its R&D pipeline with the aim of enhancing its product offering, adding new indications and bringing new products to market. |
||
| See chapter Innovation at Grifols for more information | ||
| Disruptive Changes in Main Products |
Grifols faces significant market competition. Its current and future competitors may increase their sales, lower their prices, change their distribution model or improve their products, undermining Grifols' product sales and market share. |
|
| To address these challenges, the company is actively engaged in innovation scouting to analyze the competitive and technological landscape, identify emerging threats and develop strategies to mitigate these risks. |
||
| See chapter Innovation at Grifols for more information | ||
| IT Governance | Ineffective IT governance poses significant risks in today's data-driven world, including data breaches, regulatory non-compliance, operational inefficiencies, financial losses and hindered innovation. |
|
| To ensure effective IT governance, the company is enhancing its comprehensive IT governance framework in alignment with international standards and best practices. |
||
| Ethics and Integrity | Grifols' business is subject to extensive government regulation and oversight in its numerous markets of operation. The promotion, marketing and sale of pharmaceutical products and medical devices is highly regulated and subject to increasing governmental supervision around the world. This regulatory and oversight trend is expected to continue. |
|
| The company has enacted anticorruption, anticompetition, privacy, healthcare and corporate compliance policies and procedures to govern its business practices, including distributors and suppliers. |
||
| See chapter Ethics, integrity and human rights are at the heart of Grifols' corporate culture for more information |
||
| Supply Chain | A significant disruption in Grifols' supply of plasma could have a material adverse effect on its business and growth plans. Most of its revenue relies on its access to U.S. source plasma (plasma obtained through plasmapheresis), the main raw material for Grifols' plasma derivative products. |
|
| Over the last few years, pursuant to the implementation of its business strategy, Grifols acquired plasma collection centers in the U.S., Europe and Canada. In 2024, the company continued to expand its network of plasma collection centers, particularly in the United States, while also implementing initiatives to increase plasma and manufacturing efficiencies. As most of its plasma is sourced internally, Grifols is well positioned to ensure the availability of plasma for its manufacturing needs and the quality of plasma throughout the production process. |

| Risk | Assessment and Mitigation Activities |
|---|---|
| Manufacturing Concentration |
The company's production capacity is highly concentrated in a few manufacturing plants, making it vulnerable to disruptions from extreme weather events (e.g., hurricanes, droughts, floods) and critical accidents (e.g., fires, explosions). These disruptions could lead to financial losses and operational downtime. |
| To mitigate these risks, the company has established the following mitigation action plans: (i) the manufacturing plants are licensed by various regulators, providing the flexibility to perform processes interchangeably; (ii) disaster recovery plans are in place; and (iii) the manufacturing plants are insured against extreme weather events and critical accidents. |
|
| See chapter Climate Change - Adaptation for more information | |
| U.S. Biopharma Pricing and Demand |
The existence of direct and indirect price controls and pressures over Grifols' products have affected, and may continue to affect, its ability to maintain or increase gross margins. |
| Proposed U.S. federal and state legislation have targeted drug pricing, including direct negotiations with manufacturers over price, reimbursement and discounts. Plasma protein therapeutics have been excluded from certain aspects of the several legislations. However, there is a continuing risk that Grifols' products may be subject to new pricing restrictions. |
|
| Despite these challenges, the company has experienced robust revenue growth across key geographies, along with margin expansion driven by product mix, lower cost per liter and operational leverage. The achievement of key innovation milestones and the acceleration of the research and development pipeline to enhance the product portfolio, introduce new indications and bring new products to market will help mitigate the potential impact of price controls and pressures. |
|
| Talent Retention and Attraction |
Grifols' future success depends on its ability to retain members of its senior management and capacity to attract, retain and motivate qualified personnel. The company is highly dependent on the core members of its executive and scientific teams. For this reason, the recruitment and retention of qualified operations, finance and accounting, scientific, clinical and sales and marketing personnel will be critical to its success. |
| The company has established a comprehensive rewards model to enhance employees' experience built upon four main pillars: compensation and benefits, development, recognition, and positive work environment. Additionally, work climate surveys are conducted periodically to gather regular feedback from employees, with mitigation plans implemented based on the survey results. |
|
| See chapter Our people for more information | |
| Integration of Advanced Technologies |
Adopting new technologies, such as artificial intelligence and cloud computing, offers both opportunities and risks. These technologies have the potential to disrupt existing business models and necessitate substantial investments in new skills and infrastructure. Ineffective integration of these technologies could adversely affect our competitive position and financial performance. Digital innovation is a core hub in Grifols' operations, allowing the company to detect market opportunities and better compete in today's fast-paced business landscape See chapter Innovation at Grifols - Digital innovation for more information |
| Product Safety and Quality | Noncompliance with quality and safety regulations could potentially harm the health and safety of patients, donors and/or participants in clinical trials, lead to product liability claims or product recalls, resulting in significant financial losses and negative reputation impacts. |
| The company has a robust quality management system and vigilance system for medical devices, pharmacovigilance and surveillance system and clinical quality system |
|
| See chapter Patients and healthcare professionals - Striving for excellence in our value chain for more information |
Grifols' risk management process includes the identification and evaluation of emerging risks, understood as new risks or risks which, although known, arise in a new or unfamiliar context and could wield a potential long-term impact on the company's activity.
| Risk | Impacto potencial | Plan de acciones mitigadoras |
|---|---|---|
| Growing Trade Protectionism / Economic Nationalism The escalating trade tensions between the United States and China present a complex and multifaceted risk to Grifols' operations given its substantial presence in both markets. Although difficult to anticipate, these tensions are expected to intensify in the near future, driven by the new U.S. administration's policies aimed at protecting domestic economic interests, and China's growing focus on achieving self-sufficiency in key industries, including the plasma industry. |
The U.S. and China may adopt protectionist measures to safeguard their respective economies. These policies could include higher tariffs on imported goods, stricter import restrictions, and incentives to boost domestic production. Such measures could adversely impact the company's sales and profitability, disrupt its supply chain, increase operational costs, reduce the competitiveness of Grifols products in these markets, and potentially restrict market access. |
To mitigate these risks, the company is adopting proactive risk management strategies and continuous monitoring geopolitical developments. This includes diversifying of manufacturing and supply chain across different regions, reducing reliance on any single country or region and enhancing resilience against supply chain disruptions. Additionally, through the strategic alliance with Haier Group following the sale of a 20% equity stake in Shanghai RAAS (SRAAS), the company and SRAAS have extended their exclusive albumin distribution agreement over the next 10 years, with guaranteed minimum volumes between 2024 and 2028, with an option to extend the agreement until 2044. |
| Advanced Cybercrime Threats The landscape of cyberattacks is continuously evolving, characterized by increasing complexity and innovation. The integration of artificial intelligence and quantum computing with conventional cyber threats is expected to significantly enhance both the sophistication and frequency of these attacks. As a global healthcare company, Grifols is particularly exposed to cyberattacks due to the high value of medical and pharmaceutical records. Its increasing reliance on digital storage and exchange of sensitive data further exacerbates this vulnerability. |
Future cyberattacks on Grifols' IT systems may result in the loss of financial data or operational disruptions, which could materially and adversely affect its business, financial condition, future operational results and reputation. |
Grifols' current main cybersecurity measures are outlined in the "Cybersecurity" chapter. To address advanced cybercrime risks, the company is implementing additional controls and automated detection and response systems, and continuously scanning new intrusion prevention and detection tools. If these measures fail to prevent system or data damage, the company has response and recovery programs, and insurance coverage for cyber risks. |
A solid risk culture is essential for organizations to effectively identify, assess and manage the risks that could impact their operations. Grifols delivers training and awareness programs to encourage employees throughout the organization to identify risks and work to actively mitigate them, as well as promotes transparent communications among employees in risk related functions.
Grifols has established a comprehensive risk culture in alignment with its corporate strategy, which encompasses the following elements:
● Training: Grifols develops and imparts training and awarenessraising plans to ensure employees have a solid theoretical foundation and practical knowledge of environmental issues, health and safety, compliance, cybersecurity, crime prevention, pharmacovigilance and quality, among other risk areas.
Members of the Audit Committee receive regular training on new governance requirements and trends. Additionally, another nonexecutive member of Grifols' Board of Directors has proven experience in risk management and control and, from his leadership role, contributes to fostering a risk management culture throughout the company.
3 core levers Tax policy Governance Legal compliance
Grifols is firmly committed to driving economic, social and industrial progress through compliance with applicable tax legislation in its countries of operation, paying its fair share in jurisdictions where it creates value. Its corporate structures are based on commercial and industrial rationale, aligned with its business activities, and backed by tangible impact. Grifols has no presence in territories classified as tax havens.
Grifols' Tax Policy defines the principles guiding its fiscal management. As a key aspect of corporate responsibility, taxation is overseen by the Board of Directors, whose responsibilities include approving and regularly monitoring the group's Tax Policy to ensure alignment with its business operations and sustainability commitments. Grifols' senior management, under the supervision of the Board, is tasked with developing the group's tax strategy and compliance framework. That said, other organizational areas, engaged in both routine and non-routine tasks, may contribute to its implementation.

The company strives to develop cooperative relationships with tax authorities grounded in respect, transparency and mutual trust. On October 26, 2018, Grifols' Board of Directors adhered to Spain's Code of Good Tax Practices, underscoring its unequivocal commitment to transparency, good faith and cooperation. As part of its commitment to transparency, the company regularly reports its tax strategy and taxes paid. In addition, it also reports and details controversies and possible litigation in tax matters, if any, in the Consolidated Annual Accounts and in information to market regulators.
Grifols' Board of Directors, mainly composed by independent directors, approves the Risk Control and Management Policy, which outlines the core principles and framework to identify, evaluate, monitor and manage all types of risks, including tax risks, faced by the company and its affiliates.
The Audit Committee supervises the effectiveness of internal control, internal auditing and risk management systems, including those related to tax issues. It regularly reviews these systems to ensure that key risks are adequately identified, managed and reported.
The Internal Audit Department assists the Audit Committee by:
The Corporate Risk Committee oversees the responsibilities of Grifols' leadership team in risk assessment, management and control, ensuring the integration of robust risk management processes within the established system.
Grifols complies with current tax legislation in its countries of operation and the OECD Guidelines for Multinational Enterprises. In the United States, the company complies with, subscribes to and reports on the Tax Control Framework Questionnaire (2019), prepared by the U.S. Internal Revenue Service (IRS).
This initiative complements the OECD Model Control of Tax Risks standard by including a self-assessment mechanism to cover core elements in the tax risk management and control system. The principles guiding Grifols' risk management and control system are subject to tax risks, which fall under the category of legal and regulatory risks.
Reflecting its commitment to transparency, Grifols reports its tax contribution from three different perspectives: contribution by tax, tax value distribution and contribution by geographical area. For this purpose, Grifols follows PwC's Total Tax Contribution (TTC) methodology, which measures the total impact of tax payments made by a company.
This methodology aligns with the OECD's approach, which emphasizing the importance of the role of businesses in the tax system, both as taxpayers (input taxes) and tax collectors on behalf of third parties (taxes collected). The scope of this analysis covers Grifols' main countries of operation: Spain, the United States, Ireland and Germany. Taxes are classified as follows:
Grifols' diverse activities generate direct and collected taxes, which are paid to global tax authorities. In general terms, these highly integrated activities can be classified into net interest, wages and salaries, taxes (input and collected) and shareholder value.
The distributed tax value (DTV) ratio shows the percentage of Grifols' value generation that is allocated to pay taxes borne and collected from Public Administrations.

The DTV ratio stands at 24% globally for Grifols. This means that 24% of the value generated by Grifols has been contributed to the public treasury through taxes paid (11%) and taxes collected (13%). In other words, out of every EUR 100 of value generated in 2024, Grifols has allocated EUR 24 toward tax payments.
Total tax contribution in 2024
EUR 348 M
reflecting a 6% increase over 2023 and a 60% increase over the last 3 years.
EUR 401 M
a 9% increase compared to 2023 and an 18% increase over the past 3 years
Taxes on profits account for 43% of the taxes paid. 70% of the taxes paid and collected are related to employment: 49% of taxes paid and 86% of taxes collected.
Grifols' tax policy establishes responsible conduct in tax matters, embracing principles consistent with those set forth in OECD Guidelines for Multinational Enterprises (2011). The policy explicitly states that Grifols has no presence in jurisdictions classified as tax havens, and its commercial operations with third parties in these territories or any other territories form part of its ordinary manufacturing and commercial activity.
Grifols is taxed on the profits generated in each of its countries of operation. Spain, the United States, Ireland and Germany account for more than 70% of the group's global revenue. These countries are also where its main industrial installations and R+D+i facilities are located.
The grants received are mainly allocated to initiatives focused on employee training and job creation.
| Thousands of Euros | Grants |
|---|---|
| U.S. | 18,292 |
| Spain | 494 |
| Profit* | Taxes paid** | Total tax | ||
|---|---|---|---|---|
| (Thousands of euros) | (Thousands of euros) | contribution*** | % | |
| U.S. | 346,380 | 77,690 | 408 M | 55% |
| Spain | 45,276 | 43,646 | 22 2M | 30% |
| Ireland | 314,190 | 42,307 | 65 M | 9% |
| Germany | 87,743 | 14,572 | 53 M | 7% |
| RoW | 57,252 | 11,293 | NAP | NAP |
* Profit after tax in 2024, excluding dividends and impairments or disposals in Group Companies.
** Net tax payable for the 2024 fiscal year (Corporate income tax)
*** Total Tax Contribution (TTC) in the United States: the exchange rate applied was 1.039 euros/dollar. In the U.S., the total contribution decreased compared to the previous year due to adjustments made under the operational improvement plan. The calculation of the Total Tax Contribution excludes Biotest and other entities from RoW.

Note: The Total Tax Contribution (TTC) ratio is an indicator of the cost of taxes paid in relation to the profits obtained. The calculation is made as the percentage of taxes paid relative to the profit before those taxes in each territory, taking into account the aggregate figures of the entities involved in the study.
*Ireland: Although the ratio is significantly lower than in other territories, a notable trend has been observed. It was not possible to calculate the TTC ratio in the previous fiscal year since the company recorded negative results. Ireland has also seen a significant increase in its Total Tax Contribution (+29% compared to 2023).
**Spain: the TTC ratio is distorted (close to 100%) due to the exclusion of profits from Grifols' divestitures in 2024 and the payment of related taxes abroad. As a result, the ratio reflects that Grifols' tax payments in Spain are close to the Profit Before Tax in this territory.
CONTENIDOS
| Indices of content according to regulations | 210 |
|---|---|
| Content required by the Law 11/2018. of December 28 | 210 |
| Disclosure requirements in ESRS covered by the Sustainability statement (ESRS 2 - IRO 2) |
214 |
| Data points that are included and derive from other EU legislation (ESRS 2 - BP 2) |
218 |
| Methodologies | 222 |
| Calculation of the adjusted and unadjusted pay gap | 222 |
| Total Tax Contribution | 224 |
| Glossary and abbreviations | 225 |
| Independent Review Report | 228 |

| LAW 11/2018 CONTENT INDEX | |||
|---|---|---|---|
| Information requested by the Law 11/2018 | Materiality | Page number(s) | Reporting criteria |
| General information | |||
| A brief description of the business model that includes its business environment, its organization and structure |
Material | 4-8, 175-180 | |
| Markets in which it operates | Material | 5-6 | ESRS 2 SBM1 |
| Objectives and strategies of the organization | Material | 9-11 | ESRS 2 SBM2 |
| Main factors and trends that can affect its future evolution | Material | 202-204 | ESRS 2 SBM3 ESRS 2 GOV1 |
| Reporting framework used | Material | 19-20 | |
| Principle of materiality | Material | 15-18 | |
| Environmental Issues | |||
| Management approach: description and results of the policies related to these issues, as well as the main risks related to those issues related to the group's activities. |
Material | 23-25, 37, 39, 56, 61, 69, 71 | GOV-4 IRO-1 E1.IRO-1 E2.IRO-1 E3.IRO-1 E4.IRO-1 E5.IRO-1 E1-2 E1-3 E2-1 E2-2 E3-1 E3-2 E4-2 E4-3 E5-1 E5-2 |
| Detailed general information | |||
| Detailed information on the actual and predictable effects of the company's activities on the environment and, when applicable, health and safety. |
Material | 37, 56, 61, 69, 71 | ESRS 2 IRO-1 E1.IRO-1 E2.IRO-1 E3.IRO-1 E4.IRO-1 E5.IRO-1 |
| Environmental assessment or certification procedures | Material | 24 | ESRS 2 BP2 |
| Resources dedicated to the prevention of environmental risks | Material | 26 | E1-3 E2-2 E3-2 E4-3 E5-2 |
| Application of the precautionary principle | Material | 23 | ESRS 2 MDR - A |
| Amount of provisions and guarantees for environmental risks | Material | 25 | GRI 3-3 |
| Contamination | |||
| Measures to prevent, reduce or repair emissions that seriously affect the environment; considering any form of activity-specific air pollution, including noise and light pollution |
Not material | 56-60 | E2-2 |
| Circular Economy and Waste Prevention and Management | |||
| Prevention, recycling, reutilization and other recovery and waste disposal measures. | Material | 71-80 | E5-2 E5-5 |
| Actions to fight food waste | Not material | - | E5-2 |
| GRIFOLS | |
|---|---|
| --------- | -- |
| General Environment |
Social | Governance | Annexes Indices of content according to regulations |
|
|---|---|---|---|---|
| LAW 11/2018 CONTENT INDEX | ||||
| Information requested by the Law 11/2018 | Materiality | Page number(s) | Reporting criteria | |
| Sustainable Use of Resources | ||||
| Water consumption and supply in accordance with the local limitations | Material | 61-68 | E3-4 | |
| Consumption of raw materials and measures taken to improve the efficiency of their use | Material | 71-74, 77 | E5-2 E5-4 |
|
| Direct and indirect energy consumption | Material | 45-47, 50-55 | E1-5 E1-2 E1-3 |
|
| Measures taken to improve energy efficiency | Material | 42-43, 45-47 | E1-5 | |
| Use of renewable energy | Material | 42-43, 45-47 | E1-5 | |
| Climate Change | ||||
| Greenhouse gas emissions generated as a result of the company's activities, including the use of the goods and services it produces |
Material | 41-44, 48-50 | E1-6 | |
| Measures taken to adapt to the consequences of climate change | Material | 41 | E1-3 | |
| Voluntary measures for medium and long-term reduction goals to reduce greenhouse gas emissions and the means implemented for this purpose |
Material | 40, 42, 43, 48-49 | E1-4 | |
| Biodiversity Protection | ||||
| Measures taken to preserve or restore biodiversity | Not material | 69-70 | E4-1 E4-3 |
|
| Impacts caused by activities or operations in protected areas | Not material | 69-70 | E4.SBM-3 E4.IRO-1 E4-5 |
|
| Social and Personnel matters | ||||
| Management approach: description and results of the policies related to these matters as well as the main risks related to those issues linked to the group's activities. |
Material | 83, 179, 202-203 | GOV-4 IRO-1 S1-1 S1-2 S1-3 S1-4 ESRS 2 IRO 1 |
|
| Employment | ||||
| Total number and distribution of employees by country, gender, age and professional category |
Material | 85, 102-110 | S1-6 S1-9 GRI 2-7 GRI 2-8 |
|
| Total number and distribution of employment contract modalities and annual average of indefinite contracts, temporary contracts and part-time contracts by gender, age and professional category |
Material | 102-110 | S1-6 GRI 2-7 GRI 2-8 |
|
| Number of dismissals by gender, age and professional classification | Material | 114-115 | S1-6 GRI 401-1 |
|
| Average remuneration and its evolution disaggregated by sex, age and professional classification or equal value |
Material | 122-126 | S1-10 S1-16 GRI 405-2 |
|
| Gender gap, the remuneration of equal or average company jobs | Material | 100-101, 126-127 | S1-16 | |
| Average remuneration of directors and executives, including variable remuneration, allowances, allowances, payment to long-term savings forecasting systems and any other perception disaggregated by sex |
Material | 121, 126, 181-182 | GRI 2-19 GRI 3-3 |
|
| Implementation of policies work disconnection | Material | 82-83, 88 | S1-1 | |
| Number of employees with disabilities | Material | 96, 98 | S1-12 |
|---|---|---|---|
| Organization of Work | |||
| Organization of working time | Material | 88-89 | S1-15 |
| Number of hours of absenteeism | Material | 115-117 | GRI 3-3 GRI 403-9 GRI 403-10 |
| Measures aimed at facilitating the enjoyment of conciliation and promoting the co responsible exercise of these by both parents |
Material | 82-83, 87-88, 120-121 | S1-4 S1-15 |
| Health and Safety | |||
| Health and safety conditions at work | Material | 90-91 | S1-1 S1-14 |
| Occupational accidents, their frequency and severity, as well as occupational diseases; disaggregated by gender |
Material | 122-123 | S1-14 GRI 403-9 GRI 403-10 |
| GRIFOLS | |
|---|---|
| --------- | -- |
Indices of content according to regulations
| LAW 11/2018 CONTENT INDEX | |||
|---|---|---|---|
| Information requested by the Law 11/2018 | Materiality | Page number(s) | Reporting criteria |
| Social Relationships | |||
| Organization of social dialogue including procedures for informing and consulting staff and negotiating with them |
Material | 86-87, 89 | S1-8 |
| Mechanisms and procedures that the company has to promote the involvement of workers in the management of the company, in terms of information, consultation and participation |
Material | 89-90 | S1-8 |
| Percentage of employees covered by collective agreement by country | Material | 89 | S1-8 |
| Balance of collective agreements, particularly in the field of health and safety at work | Material | 89-90 | S1-8 S1-14 |
| Training | |||
| Policies implemented in the field of training | Material | 83, 92-95 | S1-1 S1-13 |
| Total number of training hours by professional category | Material | 117-119 | S1-13 GRI 3-3 GRI 404-1 |
| Universal accessibility | |||
| Integration and universal accessibility of people with disabilities | Material | 98 | S1-1 S1-12 |
| Equality | |||
| Measures taken to promote equal treatment and opportunities for women and men | Material | 83, 96, 99-100 | S1-4 S1-9 |
| Equality plans, measures taken to promote employment, protocols against sexual and gender harassment |
Material | 97-101 | S1-1 S1-4 |
| Policy against all types of discrimination and, when applicable, diversity management | Material | 83, 96-101 | S1-1 S1-9 |
| Respect for human rights | |||
| Management approach: description and results of the policies related to these matters as well as the main risks related to those issues linked to the group's activities. |
Material | 128, 183-184 | GOV-4 IRO-1 S1-1 S1-2 S1-3 S1-4 ESRS 2 IRO 1 |
| Aplicación de procedimientos de diligencia debida | |||
| Application of due diligence procedures in the field of human rights and prevention of risks of violation of human rights and, where appropriate, measures to mitigate, manage and repair possible abuses committed |
Material | 130, 185-186, 189-190 | ESRS 2 GOV 4 S1-1 |
| Complaints for cases of human rights violation | Material | 129, 190 | S1-17 |
| Measures implemented to promote and comply with the provisions of the ILO fundamental conventions related to respect for freedom of association and the right to collective bargaining; the elimination of discrimination in employment and occupation; the elimination of forced or compulsory labor; the effective abolition of child labor |
Material | 83, 129, 185 | S1-1 |
| Fight against corruption and bribery | |||
| Management approach: description and results of the policies related to these matters as well as the main risks related to those issues linked to the group's activities. |
Material | 183-184 | G1-1 ESRS 2 IRO 1 |
| Measures taken to prevent corruption and bribery | Material | 184, 186-188, 190 | G1-3 |
| Measures to fight money laundering | Material | 186-190 | G1-3 |
| Contributions to foundations an NGOs | Material | 195 | GRI 2-28 GRI 201-1 GRI 415-1 |
| Information about society | |||
| Management approach: description and results of the policies related to these matters as well as the main risks related to those issues linked to the group's activities. |
Material | 131, 147, 192-194, 202-203, 205- 206 |
GOV-4 IRO-1 S3-1 S4-1 G1-1 ESRS 2 IRO 1 |
Indices of content according to regulations
| LAW 11/2018 CONTENT INDEX | |||
|---|---|---|---|
| Information requested by the Law 11/2018 | Materiality | Page number(s) | Reporting criteria |
| Commitment of the company to sustainable development | |||
| The impact of the company's activity on employment and local development | Material | 137-145 | ESRS 2 SBM 3 S3-1 S3-4 |
| The impact of society's activity on local populations and in the territory | Material | 137-145 | ESRS 2 SBM 3 |
| The relations maintained with the actors of the local communities and the modalities of the dialogue with these |
Material | 13 - 14, 132 | S3-2 |
| Partnership or sponsorship actions | Material | 13, 139, 141, 144-145 | GRI 3-3 GRI 201-1 |
| Subcontracting and suppliers | |||
| Inclusion in the purchasing policy of social, gender equality and environmental issues | Material | 192-194 | G1-1 |
| Consideration in the relations with suppliers and subcontractors of their social and environmental responsibility |
Material | 192-194 | G1-2 |
| Supervision and audit systems and their results | Material | 150-152, 194 | GRI 414-2 GRI 308-2 |
| Consumers | |||
| Measures for the health and safety of consumers | Material | 150-154 | S4-4 |
| Complaint systems, complaints received and resolution thereof | Material | 154 | S4-3 |
| Tax information | |||
| Profit obtained country by country | Material | 208 | GRI 207-4 |
| Taxes earned on benefits paid (per country) | Material | 208 | GRI 207-4 |
| Public grants received (per country) | Material | 208 | GRI 201-4 |
| EU Taxonomy | Material | 28-36 | KPIs developed according to the methodology described in this report |
Appendix B
List of datapoints in cross-cutting and topical standards that derive from other EU legislation
This appendix is an integral part of the ESRS 2. The table below illustrates the datapoints in ESRS 2 and topical ESRS that derive from other EU legislation.
| DISCLOSURE REQUIREMENTS CONTENTS |
PAGE NUMBER | ||
|---|---|---|---|
| GENERAL DISCLOSURES | |||
| ESRS 2 General disclosures | |||
| Basis for preparation |
DR BP-1 | General basis for preparation of sustainability statements | 19-20 |
| DR BP-2 | Disclosures in relation to specific circumstances | 19-20 | |
| DR GOV-1 | The role of the administrative, management and supervisory bodies | 20, 176-181 | |
| Governance | DR GOV-2 | Information provided to and sustainability matters addressed by the undertaking's administrative, management and supervisory bodies |
20-21, 180 |
| DR GOV-3 | Integration of sustainability-related performance in incentive schemes | 25, 181-182 | |
| DR GOV-4 | Statement on due diligence | 21 | |
| DR GOV-5 | Risk management and internal controls over sustainability reporting | 20-21 | |
| DR SBM-1 | Strategy, business model and value chain | 4-9, 175 | |
| Strategy | DR SBM-2 | Interests and views of stakeholders | 13-14 |
| DR SBM-3 | Material impacts, risks and opportunities and their interaction with strategy and business model |
17-18, 37-39, 56, 61, 69, 71, 82, 128, 131, 146, 163, 183, 196, 202-204 |
|
| DR IRO-1 | Description of the process to identify and assess material impacts, risks and opportunities |
15-17, 201-202 | |
| Impact, risk and opportunity management |
DR IRO-2 | Disclosure requirements in ESRS covered by the undertaking's sustainability statement |
214-218 |
| MDR-P | Policies adopted to manage material sustainability matters | 24, 40, 56, 61, 69, 72, 83, 129, 131, 147, 164, 184, 196 |
|
| MDR-A | Actions and resources in relation to material sustainability matters | 24, 40, 56, 61, 69, 72, 83, 129, 131, 147, 164, 184, 196 |
|
| Metrics and targets |
MDR-M | Metrics in relation to material sustainability matters | 24, 40, 56, 61, 69, 72, 83, 129, 131, 147, 164, 184, 196 |
| MDR-T | Tracking effectiveness of policies and actions through targets | 24, 40, 56, 61, 69, 72, 83, 129, 131, 147, 164, 184, 196 |
|
| TOPIC-SPECIFIC ENVIRONMENTAL STANDARDS | |||
| ESRS E1 Climate change | |||
| Governance | DR related to ESRS 2 GOV-3 |
Integration of sustainability-related performance in incentive schemes | 25 |
| DR E1-1 | Transition plan for climate change mitigation | 41 | |
| Strategy | DR related to ESRS 2 SBM-3 |
Material impacts, risks and opportunities and their interaction with strategy and business model |
37, 39 |
| Impact, risk and |
DR related to ESRS 2 IRO-1 |
Description of the processes to identify and assess material climate-related impacts, risks and opportunities |
15-17, 38, 201-202 |
| opportunity | DR E1-2 | Policies related to climate change mitigation and adaptation | 24, 40 |
| management | DR E1-3 | Actions and resources in relation to climate change policies | 26-27, 40-42 |
| DR E1-4 | Targets related to climate change mitigation and adaptation | 43 | |
| DR E1-5 | Energy consumption and mix | 45-47, 50-55. Quantitative energy-related information is reported in kilowatt hours (kWh). To obtain data in Mega-Watt- hours (MWh), the value must be divided by 1000. |
|
| Metrics and targets |
DR E1-6 | Gross Scopes 1, 2, 3 and Total GHG emissions | 44, 48-50 |
| DR E1-7 | GHG removals and GHG mitigation projects financed through carbon credits | 44 | |
| DR E1-8 | Internal carbon pricing | 44 | |
| DR E1-9 | Anticipated financial effects from material physical and transition risks and potential climate-related opportunities |
39 |


Indices of content according to regulations
| DISCLOSURE REQUIREMENTS CONTENTS |
PAGE NUMBER | ||
|---|---|---|---|
| ESRS E2 Pollution | |||
| Impact, | DR related to ESRS 2 IRO-1 |
Description of the processes to identify and assess material pollution-related impacts, risks and opportunities |
15-17, 201-202 |
| risk and opportunity |
DR E2-1 | Policies related to pollution | 56-57 |
| management | DR E2-2 | Actions and resources related to pollution | 26-27, 56-57 |
| DR E2-3 | Targets related to pollution | 56-57 | |
| DR E2-4 | Pollution of air, water and soil | 58-60. Soil and air pollution is not material. | |
| Metrics and targets |
DR E2-5 | Substances of concern and substances of very high concern | 58. Not material. |
| DR E2-6 | Anticipated financial effects from pollution-related impacts, risks and opportunities |
Grifols is working to expand this information. | |
| ESRS E3 Water and marine resources | |||
| Impact, risk and |
DR related to ESRS 2 IRO-1 |
Description of the processes to identify and assess material water and marine resources-related impacts, risks and opportunities |
15-17, 201-202 |
| opportunity | DR E3-1 | Policies related to water and marine resources | 61-62 |
| management | DR E3-2 | Actions and resources related to water and marine resources | 26-27, 61-62 |
| DR E3-3 | Targets related to water and marine resources | 61-62 | |
| Metrics and | DR E3-4 | Water consumption | 63-68 |
| targets | DR E3-5 | Anticipated financial effects from water and marine resources-related impacts, risks and opportunities |
Grifols is working to expand this information. |
| ESRS E4 Biodiversity and ecosystems | |||
| DR E4-1 | Transition plan and consideration of biodiversity and ecosystems in strategy and business model |
Not material | |
| Strategy | DR related to ESRS 2 SBM-3 |
Material impacts, risks and opportunities and their interaction with strategy and business model |
69 |
| Impact, risk and |
DR related to ESRS 2 IRO-1 |
Description of processes to identify and assess material biodiversity and ecosystem-related impacts, risks and opportunities |
15-17, 201-202 |
| opportunity | DR E4-2 | Policies related to biodiversity and ecosystems | Not material |
| management | DR E4-3 | Actions and resources related to biodiversity and ecosystems | Not material |
| DR E4-4 | Targets related to biodiversity and ecosystems | Not material | |
| Metrics and | DR E4-5 | Impact metrics related to biodiversity and ecosystems change | Not material |
| targets | DR E4-6 | Anticipated financial effects from biodiversity and ecosystem-related risks and opportunities |
Not material |
| ESRS E5 Resource use and circular economy | |||
| Impact, risk and |
DR related to ESRS 2 IRO-1 |
Description of the processes to identify and assess material resource use and circular economy-related impacts, risks and opportunities |
15-17, 201-202 |
| opportunity | DR E5-1 | Policies related to resource use and circular economy | 72-73 |
| management | DR E5-2 | Actions and resources related to resource use and circular economy | 26-27, 72-76 |
| DR E5-3 | Targets related to resource use and circular economy | 72 | |
| Metrics and targets |
DR E5-4 | Resource inflows | 74. Grifols is working to expand this information. |
| DR E5-5 | Resource outflows | 75 | |
| DR E5-6 | Anticipated financial effects from resource use and circular economy-related impacts, risks and opportunities |
Grifols is working to expand this information. | |
| TOPIC-SPECIFIC SOCIAL STANDARDS | |||
| ESRS S1 Own workforce | |||
| DR related to ESRS 2 SBM-2 |
Interests and views of stakeholders | 13-14, 84 | |
| Strategy | DR related to ESRS 2 SBM-3 |
Material impacts, risks and opportunities and their interaction with strategy and business model |
82-83 |
| GRIFOLS | |||||
|---|---|---|---|---|---|
| --------- | -- | -- | -- | -- | -- |


| DISCLOSURE REQUIREMENTS | CONTENTS | PAGE NUMBER | |||
|---|---|---|---|---|---|
| Impact, risk and opportunity management |
DR S1-1 | Policies related to own workforce | 83, 185 | ||
| DR S1-2 | Processes for engaging with own workforce and workers' representatives about impacts |
89 - 90 | |||
| DR S1-3 | Processes to remediate negative impacts and channels for own workforce to raise concerns |
83-84, 97-98, 185, 189-190 | |||
| DR S1-4 | Taking action on material impacts on own workforce, and approaches to managing material risks and pursuing material opportunities related to own workforce, and effectiveness of those actions |
82-83 | |||
| DR S1-5 | Targets related to managing material negative impacts, advancing positive impacts, and managing material risks and opportunities |
82-83 | |||
| DR S1-6 | Characteristics of the undertaking's employees | 102-115 | |||
| DR S1-7 | Characteristics of non-employees in the undertaking's own workforce | Grifols is working to expand this information. | |||
| DR S1-8 | Collective bargaining coverage and social dialogue | 89 | |||
| DR S1-9 | Diversity metrics | 102, 104, 106, 108-109 | |||
| DR S1-10 | Adequate wages | 86-87 | |||
| Metrics and | DR S1-11 | Social protection | 87-88 | ||
| targets | DR S1-12 | Persons with disabilities | 96 | ||
| DR S1-13 | Training and skills development metrics | 117-118, 120 | |||
| DR S1-14 | Health and safety metrics | 90-91, 122-123. Grifols is working to report information related to non-employees and value chain workers. |
|||
| DR S1-15 | Work-life balance metrics | 120-121. Grifols is working to expand this information. |
|||
| DR S1-16 | Remuneration metrics (pay gap and total remuneration) | 100-101, 123-127 | |||
| DR S1-17 | Incidents, complaints and severe human rights impacts | 97-98, 189-190 | |||
| ESRS S2 Workers in the value chain | |||||
| DR related to ESRS 2 SBM-2 |
Interests and views of stakeholders | 13 | |||
| Strategy | DR related to ESRS 2 SBM-3 |
Material impacts, risks and opportunities and their interaction with strategy and business model |
128, 130, 185 | ||
| DR S2-1 | Policies related to value chain workers | 129-130 | |||
| DR S2-2 | Processes for engaging with value chain workers about impacts | 129-130 | |||
| Impact, risk and opportunity management |
DR S2-3 | Processes to remediate negative impacts and channels for value chain workers to raise concerns |
129, 189-190 | ||
| DR S2-4 | Taking action on material impacts on value chain workers, and approaches to managing material risks and pursuing material opportunities related to value chain workers, and effectiveness of those action |
128, 192-193 | |||
| Metrics and targets |
DR S2-5 | Targets related to managing material negative impacts, advancing positive impacts, and managing material risks and opportunities |
129 | ||
| ESRS S3 Affected communities | |||||
| DR related to ESRS 2 SBM-2 |
Interests and views of stakeholders | 13-14, 132 | |||
| Strategy | DR related to ESRS 2 SBM-3 |
Material impacts, risks and opportunities and their interaction with strategy and business model |
131 | ||
| DR S3-1 | Policies related to affected communities | 131-132 | |||
| DR S3-2 | Processes for engaging with affected communities about impacts | 134-137 | |||
| Impact, risk and opportunity management |
DR S3-3 | Processes to remediate negative impacts and channels for affected communities to raise concerns |
134-137, 189-190 | ||
| DR S3-4 | Taking action on material impacts on affected communities, and approaches to managing material risks and pursuing material opportunities related to affected communities, and effectiveness of those actions |
137-145 | |||
| Metrics and targets |
DR S3-5 | Targets related to managing material negative impacts, advancing positive impacts, and managing material risks and opportunities |
131 |
| General | Environment | Social | Governance | Annexes | |
|---|---|---|---|---|---|
| Indices of content according to regulations |
| DISCLOSURE REQUIREMENTS | CONTENTS | PAGE NUMBER | ||
|---|---|---|---|---|
| ESRS S4 Consumers and end-users | ||||
| Strategy | DR related to ESRS 2 SBM-2 |
Interests and views of stakeholders | 13-14, 148 | |
| DR related to ESRS 2 SBM-3 |
Material impacts, risks and opportunities and their interaction with strategy and business model |
146 | ||
| DR S4-1 | Policies related to consumers and end-users | 147 | ||
| DR S4-2 | Processes for engaging with consumers and end-users about impacts | 147-148, 155-157, 159-162 | ||
| Impact, risk and opportunity management |
DR S4-3 | Processes to remediate negative impacts and channels for consumers and end-users to raise concerns |
189-192 | |
| DR S4-4 | Taking action on material impacts on consumers and end-users, and approaches to managing material risks and pursuing material opportunities related to consumers and end-users, and effectiveness of those actions |
147, 150-162 | ||
| Metrics and targets |
DR S4-5 | Targets related to managing material negative impacts, advancing positive impacts, and managing material risks and opportunities |
147 | |
| Entity-specific topic: Innovation | ||||
| Strategy | DR related to ESRS 2 SBM-2 |
Interests and views of stakeholders | 13-14, 164 | |
| DR related to ESRS 2 SBM-3 |
Material impacts, risks and opportunities and their interaction with strategy and business model |
163, 172, 203 | ||
| Impact, risk and opportunity management |
RD relacionado con ESRS 2 IRO-1 |
Description of the processes to identify and assess material impacts, risks and opportunities |
15-17, 201-202 | |
| TOPIC-SPECIFIC GOVERNANCE STANDARDS | ||||
| ESRS G1 Business conduct | ||||
| Governance | DR related to ESRS 2 GOV-1 |
The role of the administrative, supervisory and management bodies | 20, 176-181, 199 | |||
|---|---|---|---|---|---|---|
| Impact, risk and |
RD relacionado con ESRS 2 IRO-1 |
Description of the processes to identify and assess material impacts, risks and opportunities |
15-17, 201-202 | |||
| RD G1-1 | Business conduct policies and corporate culture | 184-190, 205 | ||||
| opportunity management |
RD G1-2 | Management of relationships with suppliers | 192-194 | |||
| RD G1-3 | Prevention and detection of corruption and bribery | 184, 186-188 | ||||
| RD G1-4 | Incidents of corruption or bribery | 187, 190 | ||||
| Metrics and targets |
RD G1-5 | Political influence and lobbying activities | 191-192 | |||
| RD G1-6 | Payment practices | 194 | ||||
| Entity-specific topic: Cybersecurity | ||||||
| Governance | DR related to ESRS 2 GOV-1 |
The role of the administrative, supervisory and management bodies | 197 | |||
| Strategy | DR related to ESRS 2 SBM-2 |
Interests and views of stakeholders | 13-14 | |||
| DR related to ESRS 2 SBM-3 |
Material impacts, risks and opportunities and their interaction with strategy and business model |
196-198, 202 | ||||
| Impact, risk and opportunity management |
RD relacionado con ESRS 2 IRO-1 |
Description of the processes to identify and assess material impacts, risks and opportunities |
15-17, 201-202 |
| Disclosure Requirement and related datapoint | SFDR (1 ) reference |
Pillar 3 (2) reference |
Benchmark Regulation (3) reference |
EU Climate Law (4) reference |
Page |
|---|---|---|---|---|---|
| ESRS 2 GOV-1 Board's gender diversity paragraph 21 (d) |
x | x | 177-178 | ||
| ESRS 2 GOV-1 Percentage of board members who are independent paragraph 21 (e) |
x | 177-178 | |||
| ESRS 2 GOV-4 Statement on due diligence paragraph 30 |
x | 21 | |||
| ESRS 2 SBM-1 Involvement in activities related to fossil fuel activities paragraph 40 (d) i |
x | x | x | NAP | |
| ESRS 2 SBM-1 Involvement in activities related to chemical production paragraph 40 (d) ii |
x | x | NAP | ||
| ESRS 2 SBM-1 Involvement in activities related to controversial weapons paragraph 40 (d) iii |
x | x | NAP | ||
| ESRS 2 SBM-1 Involvement in activities related to cultivation and production of tobacco paragraph 40 (d) iv |
x | NAP | |||
| ESRS E1-1 Transition plan to reach climate neutrality by 2050 paragraph 14 |
x | 41 | |||
| ESRS E1-1 Undertakings excluded from Paris-aligned Benchmarks paragraph 16 (g) |
x | x | 41 | ||
| ESRS E1-4 GHG emission reduction targets paragraph 34 |
x | x | x | 43 | |
| ESRS E1-5 Energy consumption from fossil sources disaggregated by sources (only high climate impact sectors) paragraph 38 |
x | 45-47, 50-55 | |||
| ESRS E1-5 Energy consumption and mix paragraph 37 | x | 45-47, 50-55 | |||
| ESRS E1-5 Energy intensity associated with activities in high climate impact sectors paragraphs 40 to 43 |
x | 45-47, 50-55 | |||
| ESRS E1-6 Gross Scope 1, 2, 3 and Total GHG emissions paragraph 44 |
x | x | x | 48-49 | |
| ESRS E1-6 Gross GHG emissions intensity paragraphs 53 to 55 |
x | x | x | 49-50 | |
| ESRS E1-7 GHG removals and carbon credits paragraph 56 |
x | 43 | |||
| ESRS E1-9 Exposure of the benchmark portfolio to climate-related physical risks paragraph 66 |
x | 37-38, 41 | |||
| ESRS E1-9 Disaggregation of monetary amounts by acute and chronic physical risk paragraph 66 (a) ESRS E1-9 Location of significant assets at material physical risk paragraph 66 (c). |
x | 39 | |||
| ESRS E1-9 Breakdown of the carrying value of its real estate assets by energy-efficiency classes paragraph 67 (c). |
x | 39 | |||
| ESRS E1-9 Degree of exposure of the portfolio to climate- related opportunities paragraph 69 |
x | 39 | |||
| ESRS E2-4 Amount of each pollutant listed in Annex II of the E-PRTR Regulation (European Pollutant Release and Transfer Register) emitted to air, water and soil, paragraph 28 |
x | 58-60. Soil and air pollution is not material. |

| Disclosure Requirement and related datapoint | SFDR (1 ) reference |
Pillar 3 (2) reference |
Benchmark Regulation (3) reference |
EU Climate Law (4) reference |
Page |
|---|---|---|---|---|---|
| ESRS E3-1 Water and marine resources paragraph 9 |
x | 61-62 | |||
| ESRS E3-1 Dedicated policy paragraph 13 |
x | 61-62 | |||
| ESRS E3-1 Sustainable oceans and seas paragraph 14 |
x | 61-62 | |||
| ESRS E3-4 Total water recycled and reused paragraph 28 (c) |
x | 63-68 | |||
| ESRS E3-4 Total water consumption in m3 per net revenue on own operations paragraph 29 |
x | 63-68 | |||
| ESRS 2- IRO 1 - E4 paragraph 16 (a) i | x | Not material | |||
| ESRS 2- IRO 1 - E4 paragraph 16 (b) | x | Not material | |||
| ESRS 2- IRO 1 - E4 paragraph 16 (c) | x | Not material | |||
| ESRS E4-2 Sustainable land / agriculture practices or policies paragraph 24 (b) |
x | Not material | |||
| ESRS E4-2 Sustainable oceans / seas practices or policies paragraph 24 (c) |
x | Not material | |||
| ESRS E4-2 Policies to address deforestation paragraph 24 (d) |
x | Not material | |||
| ESRS E5-5 Non-recycled waste paragraph 37 (d) |
x | 78-79 | |||
| ESRS E5-5 Hazardous waste and radioactive waste paragraph 39 |
x | 78-79 | |||
| ESRS 2- SBM3 - S1 Risk of incidents of forced labour paragraph 14 (f) |
x | 128, 193, 203 | |||
| ESRS 2- SBM3 - S1 Risk of incidents of child labour paragraph 14 (g) |
x | 128, 193, 203 | |||
| ESRS S1-1 Human rights policy commitments paragraph 20 |
x | 83, 185-186 | |||
| ESRS S1-1 Due diligence policies on issues addressed by the fundamental International Labor Organisation Conventions 1 to 8, paragraph 21 |
x | 83, 185-186 | |||
| ESRS S1-1 processes and measures for preventing trafficking in human beings paragraph 22 |
x | 83 | |||
| ESRS S1-1 workplace accident prevention policy or management system paragraph 23 |
x | 90-91 | |||
| ESRS S1-3 grievance/complaints handling mechanisms paragraph 32 (c) |
x | 189-190 | |||
| ESRS S1-14 Number of fatalities and number and rate of work- related accidents paragraph 88 (b) and (c) |
x | x | 122-123 | ||
| ESRS S1-14 Number of days lost to injuries, accidents, fatalities or illness paragraph 88 (e) |
x | 122-123 | |||
| ESRS S1-16 Unadjusted gender pay gap paragraph 97 (a) |
x | x | 126-127 | ||
| ESRS S1-16 Excessive CEO pay ratio paragraph 97 (b) |
x | 100 | |||
| ESRS S1-17 Incidents of discrimination paragraph 103 (a) |
x | 97-98, 189-190 | |||
| ESRS S1-17 Non-respect of UNGPs on Business and Human Rights and OECD paragraph 104 (a) |
x | x | 83, 185 | ||
| ESRS 2- SBM3 – S2 Significant risk of child labour or forced labour in the value chain paragraph 11 (b) |
x | 83, 193 | |||
| ESRS S2-1 Human rights policy commitments paragraph 17 |
x | 129 | |||
| ESRS S2-1 Policies related to value chain workers paragraph 18 | x | 129-130 |
Indices of content according to regulations
| Disclosure Requirement and related datapoint | SFDR (1 ) reference |
Pillar 3 (2) reference |
Benchmark Regulation (3) reference |
EU Climate Law (4) reference |
Page |
|---|---|---|---|---|---|
| ESRS S2-1Non-respect of UNGPs on Business and Human Rights principles and OECD guidelines paragraph 19 |
x | x | 83, 185 | ||
| ESRS S2-1 Due diligence policies on issues addressed by the fundamental International Labor Organisation Conventions 1 to 8, paragraph 19 |
x | 129-130 | |||
| ESRS S2-4 Human rights issues and incidents connected to its upstream and downstream value chain paragraph 36 |
x | 129, 192-193 | |||
| ESRS S3-1 Human rights policy commitments paragraph 16 |
x | 131-132 | |||
| ESRS S3-1 non-respect of UNGPs on Business and Human Rights, ILO principles or and OECD guidelines paragraph 17 |
x | x | 132 | ||
| ESRS S3-4 Human rights issues and incidents paragraph 36 |
x | 132, 134 | |||
| ESRS S4-1 Policies related to consumers and end-users paragraph 16 |
x | 147 | |||
| ESRS S4-1 Non-respect of UNGPs on Business and Human Rights and OECD guidelines paragraph 17 |
x | x | 147 | ||
| ESRS S4-4 Human rights issues and incidents paragraph 35 |
x | 147, 150, 154 | |||
| ESRS G1-1 United Nations Convention against Corruption paragraph 10 (b) |
x | 184-186 | |||
| ESRS G1-1 Protection of whistle- blowers paragraph 10 (d) |
x | 189-190 | |||
| ESRS G1-4 Fines for violation of anti- corruption and anti-bribery laws paragraph 24 (a) |
x | x | 187 | ||
| ESRS G1-4 Standards of anti- corruption and anti- bribery paragraph 24 (b) |
x | 187-190 |
(1) Regulation (EU) 2019/2088 of the European Parliament and of the Council of 27 November 2019 on sustainability-related disclosures in the financial services sector (Sustainable Finance Disclosures Regulation) (OJ L 317, 9.12.2019, p. 1).
(2) Regulation (EU) No 575/2013 of the European Parliament and of the Council of 26 June 2013 on prudential requirements for credit institutions and investment firms and amending Regulation (EU) No 648/2012 (Capital Requirements Regulation "CRR") (OJ L 176, 27.6.2013, p. 1).
(3) Regulation (EU) 2016/1011 of the European Parliament and of the Council of 8 June 2016 on indices used as benchmarks in financial instruments and financial contracts or to measure the performance of investment funds and amending Directives 2008/48/EC and 2014/17/EU and Regulation (EU) No 596/2014 (OJ L 171, 29.6.2016, p. 1).
(4) Regulation (EU) 2021/1119 of the European Parliament and of the Council of 30 June 2021 establishing the framework for achieving climate neutrality and amending Regulations (EC) No 401/2009 and (EU) 2018/1999 ('European Climate Law') (OJ L 243, 9.7.2021, p. 1).
(5) Commission Delegated Regulation (EU) 2020/1816 of 17 July 2020 supplementing Regulation (EU) 2016/1011 of the European Parliament and of the Council as regards the explanation in the benchmark statement of how environmental, social and governance factors are reflected in each benchmark provided and published (OJ L 406, 3.12.2020, p. 1).
(6) Commission Implementing Regulation (EU) 2022/2453 of 30 November 2022 amending the implementing technical standards laid down in Implementing Regulation (EU) 2021/637 as regards the disclosure of environmental, social and governance risks (OJ L 324,19.12.2022, p.1.).
(7) Commission Delegated Regulation (EU) 2020/1818 of 17 July 2020 supplementing Regulation (EU) 2016/1011 of the European Parliament and of the Council as regards minimum standards for EU Climate Transition Benchmarks and EU Paris-aligned Benchmarks (OJ L 406, 3.12.2020, p. 17).
| GRIFOLS | ||
|---|---|---|
Indices of content according to regulations
•
The following groups were excluded from the calculation:
To ensure the consistency and representativeness of the data, the following individuals were excluded from the analysis:
In total, 19,363 people were included in the pay-gap calculation, with the following distribution by country:
| ● United States: | 13,355 |
|---|---|
| ● Spain: | 4,303 |
| ● Germany: | 1,297 |
● Ireland: 408
The pay gap was calculated in accordance with Delegated Regulation (EU) 2023/2772 of the Commission, dated July 31, 2023, which supplements Directive 2013/34/EU of the European Parliament and of the Council regarding the rules for the presentation of sustainability information, published on December 22, 2023 (hereinafter, "Delegated Regulation").
In accordance with the aforementioned Delegated Regulation: "The company shall disclose the percentage of the pay gap between female and male employees," with the gender pay gap defined as "the difference between the average pay levels of female and male employees, expressed as a percentage of the average pay level of male employees."
The calculation of the gender pay gap was based on the formula defined by the regulation:
(Average hourly pay of women- Average hourly pay of men)
Average hourly pay of men
To calculate the average remuneration, the base salary, additional fixed allowances and other types of compensation–whether in cash or in kind received directly or indirectly by the employee ("supplementary or variable components'") were taken into account.
To ensure greater consistency, it was verified that the considered remuneration met the requirements outlined in the Delegated Regulation for the ratio comparing the total annual remuneration of the highest-paid individual with the average total annual remuneration of all employees (excluding the highest-paid individual). This includes: (i) base salary, (ii) cash benefits, (iii) in-kind benefits, and (iv) direct compensation, including long-term cash benefits.
The remuneration considered was divided by the number of hours worked during the period in order to measure remuneration per unit of time.
Based on the above, the 2024 fiscal year is not comparable to previous years, which considered 100% of the fixed salary.
The Delegated Regulation specifies that the company may disclose a breakdown of the gender pay gap, as defined above, by employee category, country or segment.
The information was consequently classified by country (Spain, United States, Ireland and Germany) and professional category (Executives, Directors, Senior Management, Management, Senior Professionals, Administrative Staff/Manufacturing Operators).
The company may also disclose information on how objective factors such as job type and country of employment might influence the gender pay gap.
Unlike the "unadjusted" pay gap, adjusted pay gaps allow for isolating the effect of salaries from the differences between men and women, both in their socioeconomic characteristics (age, seniority, education level, etc.) and their positions (functional area, business unit, working conditions, etc.). For this reason, adjusted pay gaps serve as a more reliable indicator of whether men and women receive "equal pay for equal work."
To this end, the adjusted pay gap was estimated using a multiple linear regression model, which quantifies the relationship between the predictor variables (Xi1,Xi2…XiM) and the dependent variable (Wi ) through a single equation, aiming to better understand and explain the driving mechanisms behind this relationship.
In this equation, Wi represents the total hourly wage of employee i, transformed to its logarithmic value, while Gender (Genderi) is a dichotomous variable equal to 1 if male and 0 if female.
$$\ln(\mathcal{W}_l) = \beta_0 + \beta_1 \ast \text{ Sex}o_l + \sum_{l=2}^{M} \beta_l \ast X_{lj} + \mu_l$$
The econometric calculation of the adjusted pay gap considered the following variables:
Each model involves selecting variables, eliminating those deemed unnecessary and retaining only those that significantly contribute to predicting the dependent variable.
Once the model is developed, the coefficient for the Gender variable is interpreted. Its magnitude is expressed as a percentage and reveals how much the salary increases (or decreases) for being male.
The presence of an adjusted pay gap does not necessarily indicate gender discrimination. The difference may stem from additional factors (e.g., job responsibility, tenure or timing of promotion), or from missing or improbable data in the sample. As an example, individuals in higher professional categories typically earn higher salaries, yet a deterministic relationship between professional category and salary cannot be established in all cases.
A EUR/USD exchange rate of 1 euro = 1.0389 USD was applied in the preparation of the consolidated data, as per the Resolution of December 31, 2024 from the Bank of Spain, which publishes the euro exchange rates provided by the European Central Bank for that date. These rates are considered official under Article 36 of Law 46/1998, December 17 on the Introduction of the Euro.
To ensure confidentiality and protect personal data, pay gap information is not disclosed for professional categories with fewer than four (4) individuals of each gender.
In certain cases with small groups, the adjusted pay gap data is not displayed due to insufficient statistical significance in the econometric model. In these instances, only the unadjusted pay gap data is provided.
The "Fiscal Contribution" section included in the "Financial Performance" chapter provides information on the taxes paid by the Grifols Group globally in 2024 in a clear and concise manner. Disclosures includes data from the following territories: Spain, the United States, Ireland, and Germany as the most relevant in terms of their business volume and presence within the Grifols Group.
The measurement used data obtained from information systems following the PwC Total Tax Contribution (TTC) methodology. In addition to the amounts indicated, other tax payments may have been omitted because they are not individually identified in the information systems and/or are not significant in terms of materiality.
The Total Tax Contribution methodology measures the total impact of a company's tax payments. This assessment is made from the perspective of total tax contributions paid directly to the different public administrations as a result of the Grifols Group's economic activity.
In general, the TTC methodology allocates both input and output taxes to each tax year on a cash basis.
The following points should be kept in mind regarding this methodology:
Taxes borne are taxes paid by Grifols to the governments of countries in which it operates. These taxes represent an effective cost for Grifols, such as taxes on profits and certain environmental taxes.
The taxes collected are those that have been received as a result of Grifols' economic activity, without representing a cost to the Group other than that of its management. These include withholdings from workers due to income tax, VAT, and other taxes on products and services. Nonetheless, these amounts are paid into public coffers as a result of Grifols' economic activity and therefore should be included in the analysis since they represent tax revenue stemming from Grifols' operations.
Readers should take into account that figures detailed in this report include tax payments made to public administrations for items whose characteristics make them tax-related, although they have not been classified as such for cyclical or historical reasons. Readers should also take into consideration that figures in this report exclude other amounts that, based on the methodology and reports issued by the OECD and other international administrations, are not considered a tax contribution.1
The amount of profit before tax excludes intercompany dividends to avoid duplicating the same income of various entities in the case of its distribution as dividends to other Grifols entities. This calculation enables reflecting the objective amount of profit before taxes at country levels and calculating the objective ETRs, as dividends are usually subject to beneficial tax treatment compared to the other types of income (i.e. "participation exemption" regime).
Value added tax (and equivalent taxes) is characterized as a tax on products and services collected, the amount of which reflects the result of net payments made by Grifols to the tax authorities in its jurisdictions of operation in the corresponding period.
In calculating VAT, the country-specific figure indicated for this concept includes the positive amount paid to the corresponding tax authorities, resulting from subtracting the VAT accrued from the amount of VAT deducted.
No figure shall be shown for this item in cases in which the net amount resulting from subtracting VAT accrued from VAT deducted for an entire year and country is negative due to a refund.
On the other hand, VAT amounts that are not refundable because the value chain cannot be continued by means of the reverse charge instrument shall be considered as input tax on products and services, since they represent a cost for the company.
system in states of both health and disease; malfunctions (autoimmune diseases, hypersensitivities, immune deficiency, transplant rejection) and the physical, chemical and physiological characteristics of the components of the immune system in vitro, in situ and in vivo.
Zika virus: infectious disease spread by the bite of an infected Aedes species mosquito.
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