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Diasorin

Investor Presentation May 6, 2025

4129_10-q_2025-05-06_a050dc39-040d-4ad3-85f7-b090cdae56ed.pdf

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Q1 2025 RESULTS

May 6, 2025

DISCLAIMER

In General. This disclaimer applies to this presentation and any oral comments of any person presenting it. This document, taken together with any such oral comments, is referred to herein as the "Presentation". This Presentation has been prepared by Diasorin S.p.A. ("Diasorin" or the "Company" and, together with its subsidiary the "Group"). The Presentation is being furnished to you for information purposes only and for use in presentations of the industrial plan of the Group.

Verbal explanation. This Presentation has to be accompanied by a verbal explanation. A simple reading of this Presentation without the appropriate verbal explanation could give rise to a partial or incorrect understanding.

No offer to purchase or sell securities. The information, statements and opinions contained in this Presentation are for information purposes only and do not constitute a public offer under any applicable legislation or an offer to sell or solicitation of an offer to purchase or subscribe for securities or financial instruments or any advice or recommendation with respect to such securities or other financial instruments.

No distribution of this Presentation. This Presentation is being furnished to you solely for your information and may not be reproduced, in whole or in part, or redistributed to any other individual or legal entity.

Miscellanea. This Presentation has been prepared on a voluntary basis. Diasorin is therefore not bound to prepare similar presentations in the future, unless where provided by law. Neither the Company nor any member of the Group nor any of its or their respective representatives, directors, employees or agents accept any liability whatsoever in connection with this Presentation or any of its contents or in relation to any loss arising from its use or from any reliance placed upon it.

Piergiorgio Pedron, the manager responsible for the preparation of the company accounting documents for Diasorin S.p.A., declares that, pursuant to Article 154 bis, paragraph 2, of the Legislative Decree February 24, 1998, no. 58, to the best of his knowledge, the accounting information included in this Presentation correspond to document results, books and accounting records.

FORWARD-LOOKING STATEMENTS

This document contains forward-looking statements that are based on current expectations, estimates, forecasts and projections about the industries in which Diasorin operates and the beliefs and assumptions of the management of Diasorin. In addition, the management of Diasorin may make forward-looking statements orally to analysts, investors, representatives of the media and others. In particular, among other statements, certain statements regarding future financial performance, the achievement of certain targeted metrics at any future date or for any future period, trends in results of operations, margins, costs, return on capital, risk management and competition are forward-looking in nature. These statements may include terms such as "may", "will", "expect", "could", "should", "intend", "estimate", "anticipate", "believe", "remain", "on track", "design", "target", "objective", "goal", "forecast", "projection", "outlook", "prospects", "plan", or similar terms. Forward-looking statements are not guarantees of future performance and are, by their nature, subject to inherent risks, uncertainties and assumptions that are difficult to predict because they relate to events and depend on circumstances that may or may not occur or exist in the future and, as such, undue reliance should not be placed on them.

Forward-looking statements do not take into account any additional effects that may arise from impacts on the global market in which Diasorin operates and, more generally, on the macroeconomic scenario.

Actual results may differ materially from those expressed in forward-looking statements as a result of a variety of factors, including: the impact of the COVID-19 pandemic, the ability of the Group to create and launch new products successfully; changes in the global financial markets, general economic environment and changes in demand for diagnostic/healthcare/life sciences products, which is subject to cyclicality; changes in local economic and political conditions, changes in trade policy and the imposition of global and regional tariffs or tariffs targeted to the diagnostic/healthcare/life sciences industry, the enactment of tax reforms or other changes in tax laws and regulations; the Group's ability to offer innovative, attractive products; various types of claims, lawsuits, governmental investigations and other contingencies, including product liability and warranty claims, investigations and lawsuits; material operating expenditures in relation to compliance with health and safety regulations; the intense level of competition in the diagnostic/healthcare/life sciences industry, which may increase due to consolidation; the Group's ability to fund its defined benefit pension plans; the ability to access funding to execute the its business plans and improve its own businesses, financial condition and results of operations; the Group's ability to realize anticipated benefits from joint venture arrangements; disruptions arising from political, social and economic instability; commercial risk due the fact that the Group operates in a market characterized by the presence of large competitors; risk associated to the maintenance of relationship with customers and strategic partners; risks associated with relationships with employees and suppliers; increases in costs, disruptions of supply or shortages of raw materials; developments in labor and industrial relations and developments in applicable labor laws; exchange rate fluctuations, interest rate changes, credit risk and other market risks; political and civil unrest; earthquakes or other disasters.

Any forward-looking statements contained in this document speak only as of the date of this document and Diasorin disclaim any obligation to update or revise publicly forward-looking statements. Further information concerning the Group and its business, including factors that could materially affect the Group's financial results, are included in Diasorin'sreports and filings with CONSOB and Borsa Italiana.

No update. The information and opinions in this document is provided to you as of the dates indicated and Diasorin does not undertake to update the information contained in this document and/or any opinions expressed relating thereto after its presentation, even in the event that the information becomes materially inaccurate, except as otherwise required by applicable laws.

Non-IFRS and Other Performance Measures. This document contains certain items as part of the financial disclosure, which are not defined under IFRS. Accordingly, these items do not have standardized meanings and may not be directly comparable to similarly-titled items adopted by other entities. Diasorin management has identified a number of "Alternative Performance Indicators" ("APIs"). These APIs (i) are derived from historical results of Diasorin and are not intended to be indicative of future performance, (ii) are non-IFRS financial measures and, although derived from the financial statements, are unaudited and (iii) are not an alternative to financial measures prepared in accordance with IFRS. The APIs presented herein include EBITa , EBITDAb , adjusted EBITDAc , Net Financial Positiond and Free Cash Flowe . These measures are not indicative of historical operating results, nor are they meant to be predictive of future results. These measures are used by the management to monitor the underlying performance of the business and operations. Similarly entitled non-IFRS financial measures reported by other companies may not be calculated in an identical manner, consequently the measures reported in this document may not be consistent with similar measures used by other companies. Therefore, investors should not place undue reliance on this data.

a EBIT is defined as the "Operating Result" net of interests and taxes – b EBITDA is defined as the "Operating Result", gross of amortization and depreciation of intangible and tangible assets. EBITDA is a measure used by the Company to monitor and evaluate the Group's operating performance and is not defined as an accounting measure in IFRS and therefore shall not be considered an alternative measure for assessing the Group's operating result performance. c Adjusted EBITDA is defined as Adjusted EBITDA, excluding extraordinary costs and expenses incurred in the Luminex transaction announced on April 11, 2021 d The Net Financial Position is defined as the algebraic sum (positive balance sheet assets and negative balance sheet liabilities) of cash and cash equivalents and other current financial assets, minus current financial liabilities and non-current financial liabilities. e Free Cash Flow is defined as the set of means available to the Company and is equal to cash flows deriving from operating activities net of interest received or paid, and net of investments and divestments of fixed assets.

FINANCIAL HIGHLIGHTS

FINANCIAL HIGHLIGHTS

Amounts
in millions
of euros
Change
Q1
2025
@ current @ CER
Revenues 313 +8% +7%
Immunodiagnostics ex-COVID 203 +9% +8%
Molecular Diagnostics ex-COVID 56 +10% +7%
Licensed
Technologies
50 +16% +13%
COVID 5 -48% -48%
Revenues ex-COVID 309 +10% +9%
Adjusted1
EBITDA2
107 +10% +10%
Adjusted1 EBITDA2 Margin 34%
Adjusted1 EBITDA2 Margin @CER 34%
Adjusted1
EBIT
83 +13%
Adjusted1 EBIT Margin 27%
Adjusted1
Net Profit
64 +9%
% on revenues 20%
Free Cash Flow 42
Net Financial Debt -672

1 With reference to the Adjusted EBITDA, Adjusted EBIT and Adjusted Net Profit indicators, please refer to the table included in the financial schemes section of this presentation.

2 EBITDA is defined as the "Operating Result", gross of amortization and depreciation of intangible and tangible assets. EBITDA is a measure used by the Company to monitor and evaluate the Group's operating performance and is not defined as an accounting measure in IFRS and therefore shall not be considered an alternative measure for assessing the Group's operating result performance. Since the composition of EBITDA is not regulated by the reference accounting standards, the criterion of determination applied by the Group may not be homogeneous with that adopted by other operators and/or groups and therefore may not be comparable.

Q1 2025 KEY FACTS

PRODUCT & BUSINESS DEVELOPMENT

MOLECULAR DIAGNOSTICS

TARGETED

• Launch of the Simplexa® C. auris Direct assay for the LIAISON® MDX platform on all countries accepting the CE Mark

MULTIPLEX

  • FDA 510(k) clearance of the LIAISON PLEX® Gram-Negative Blood Culture Assay, the second Blood Culture panel on the LIAISON PLEX®
  • Advancement of the development of the Gastro-Intestinal panel on the LIAISON PLEX®

POINT OF CARE (POC)

• Completion of clinical studies on LIAISON NES® and on its first panel (Flu A, Flu B, COVID, RSV)

OTHER KEY FACTS

  • Diasorin constantly monitors scenarios arising from the introduction of new tariff measures that may potentially impact the Group's business areas related to the import and export of its products and the raw materials used in the production process. In a constantly evolving context, considering the current scope of the tariff measures being implemented and the mitigation actions introduced and being implemented by the Group, the impact that can be estimated on the Group's profitability is not material
  • Resolution on approval of the enhancement of the increase voting rights mechanism definitely effective and implemented
  • Appointment of the new Board Directors and the Board of Statutory Auditors

MANAGERIAL OUTLOOK ON Q1'25 REVENUES

EVOLUTION OF THE BUSINESS IN Q1'25 (@CER)

Total revenues: +7% despite lower COVID sales, in line with the FY'25 guidance.

Ex-COVID revenues: +9%, in line with FY'25 guidance:

  • Immunodiagnostic ex-COVID: +8%, mainly driven by success of U.S. Hospital Strategy and, overall, by Diasorin comprehensive specialty menu, partially offset by the impact of the VBP in China and by the unfavorable comparison with Q1'24, which was characterized by some infectious disease outbreaks in Europe.
  • Molecular diagnostic ex-COVID: +7% (+12% ex Aries platform, discontinued in 2024), as a combination of the good performance of:
    • Diasorin "targeted specialties" business;
    • Respiratory panel sales, driven by a stronger-than-average flu season;
    • "Automated multiplexing" franchise, which registered a result in line with expectations and equal to +25%.
  • Licensed technologies: +13%, mainly due to phasing of some bulk shipments to some important Diagnostic customers.

Q1'25 REVENUES BY GEOGRAPHY

(data @ current exchange rates)

Q1'25 PROFITABILITY PROFILE

(data in €/mln @ current exchange rates)

Q1'25 Adjusted1 EBITDA2 is better than last year by €/mln 10 or +10%, whereas Adjusted1 EBITDA2 Margin is in line with the previous year and consistent with the guidance, mainly as a result of the efficient cost management and operating leverage (OPEX ratio down to 37.5% from 39.5% in Q1'24).

1 With reference to the Adjusted EBITDA, Adjusted EBIT and Adjusted Net Profit indicators, please refer to the table included in the financial schemes section of this presentation.

2 EBITDA is defined as the "Operating Result", gross of amortization and depreciation of intangible and tangible assets. EBITDA is a measure used by the Company to monitor and evaluate the Group's operating performance and is not defined as an accounting measure in IFRS and therefore shall not be considered an alternative measure for assessing the Group's operating result performance. Since the composition of EBITDA is not regulated by the reference accounting standards, the criterion of determination applied by the Group may not be homogeneous with that adopted by other operators and/or groups and therefore may not be comparable.

FY 2025 COMPANY GUIDANCE

FY'25 GUIDANCE CONFIRMED

FY'25 GUIDANCE (@CER 2024)

Ex-COVID revenues: approx. +8%, approx. +7% including COVID revenues (equal to approx. 20 €/mln)

Adjusted1 EBITDA2 Margin: approx. 34%

1 With reference to the Adjusted EBITDA, Adjusted EBIT and Adjusted Net Profit indicators, please refer to the table included in the financial schemes section of this presentation. 2 EBITDA is defined as the "Operating Result", gross of amortization and depreciation of intangible and tangible assets. EBITDA is a measure used by the Company to monitor and evaluate the Group's operating performance and is not defined as an accounting measure in IFRS and therefore shall not be considered an alternative measure for assessing the Group's operating result performance. Since the composition of EBITDA is not regulated by the reference accounting standards, the criterion of determination applied by the Group may not be homogeneous with that adopted by other operators and/or groups and therefore may not be comparable.

FINANCIAL SCHEMES

INCOME STATEMENT

Amounts in millions of euros Q1 Change
2024 2025 amount %
Net Revenues 289 313 +24 +8%
Cost of sales (97) (109) -11 +11%
Gross profit 191 205 +13 +7%
66% 65% -93 bps
Sales and marketing expenses (71) (73) -2 +3%
Research and development costs (22) (24) -3 +12%
General and administrative expenses (31) (30) +1 -3%
Total operating expenses (124) (128) -4 +3%
43% 41% -206 bps
Other operating income (expense) (5) (4) +7 -11%
non recurring amount (1) (1) +7 -45%
EBIT રિક 73 +10 +15%
22% 23% +142 bps
Net financial income (expense) (4) (4) -0 +11%
Profit before taxes ਦੇ ਹੋ 69 +9 +16%
Income taxes (14) (16) -3 +19%
Net result 46 52 +7 +15%
EBITDA2 વેર 106 +11 +11%
33% 34% +90 bps

2 EBITDA is defined as the "Operating Result", gross of amortization and depreciation of intangible and tangible assets. EBITDA is a measure used by the Company to monitor and evaluate the Group's operating performance and is not defined as an accounting measure in IFRS and therefore shall not be considered an alternative measure for assessing the Group's operating result performance. Since the composition of EBITDA is not regulated by the reference accounting standards, the criterion of determination applied by the Group may not be homogeneous with that adopted by other operators and/or groups and therefore may not be comparable.

BALANCE SHEET

Amounts in millions of euros 12/31/2024 03/31/2025 Change
Goodwill and intangibles assets 2,028 1,951 -78
Property, plant and equipment 271 267 -4
Other non-current assets 34 35 +1
Net working capital 346 359 +13
Other non-current liabilities (264) (256) +8
Net Invested Capital 2,417 2,356 -60
Net Financial Debt (618) (672) -55
Total shareholders' equity 1,799 1,684 -115

CASH FLOW STATEMENT

Amounts in millions of euros Q1
2024 2025
Cash and cash equivalents at the beginning of the period 280 344
Cash provided by operating activities 75 71
Cash provided/(used) in investing activities 39 8
Cash provided/(used) in financing activities (87) 58)
Net change in cash and cash equivalents before investments in financial assets 28 21
Net change in cash and cash equivalents 28 21
Cash and cash equivalents at the end of the period 308 365

Q1'25 RECONCILIATION TO CONSOLIDATED FINANCIAL STATEMENTS

millions
of
Amounts
in
euros
Profit
Gross
EBITDA EBIT Result
Net
IFRS
Financial
Statements
Measures
205 106 73 52
%
Revenues
on
65% 34% 23% 17%
Adjustments
"One-off"
related
the
and
of
integration
restructuring
Luminex
costs
to
- 0 0 0
Depreciation
of
Luminex
intangibles
identified
in
the
Purchase
Price
Allocation
- - 10 10
Financial
charges
relating
o debt
and
o the
convertible
bond
instruments
t
t
issued
finance
the
acquisition
of
Luminex
of
hedging
effects
to
net
- - - 5
Total
adjustments
before
effect
tax
- 0 10 15
Fiscal
effect
on adjustments
- - - (4)
Total
Adjustments
- 0 10 12
Adjusted
Measures
205 107 83 64

The alternative performance measures listed in the table should be used as an information supplement to the provisions of IFRS, to assist users of the document in better understanding the economic, equity and financial performance of the Group. Such measures are computed purifying the results of the one-off costs relating to the acquisition and integration of Luminex, of the amortization deriving from the Purchase Price Allocation and of the financial charges associated with the financing of the transaction, including the tax impact. It should also be noted that the method of calculating these adjusted indicators could differ from the methods used by other companies.

Q1'24 RECONCILIATION TO CONSOLIDATED FINANCIAL STATEMENTS

millions
of
Amounts
in
euros
Profit
Gross
EBITDA EBIT Result
Net
IFRS
Financial
Statements
Measures
191 96 63 46
%
Revenues
on
66% 33% 22% 16%
Adjustments
"One-off"
of
related
the
integration
and
restructuring
Luminex
costs
to
- 1 1 1
of
intangibles
identified
the
Purchase
Depreciation
Luminex
in
Price
Allocation
- - 10 10
Financial
charges
relating
o debt
and
o the
convertible
bond
instruments
t
t
issued
finance
the
of
of
hedging
effects
acquisition
Luminex
to
net
- - - 6
Total
adjustments
before
effect
tax
- 1 11 17
Fiscal
effect
on adjustments
- - - (4)
Total
Adjustments
- 1 11 13
Adjusted
Measures
191 97 74 59

The alternative performance measures listed in the table should be used as an information supplement to the provisions of IFRS, to assist users of the document in better understanding the economic, equity and financial performance of the Group. Such measures are computed purifying the results of the one-off costs relating to the acquisition and integration of Luminex, of the amortization deriving from the Purchase Price Allocation and of the financial charges associated with the financing of the transaction, including the tax impact. It should also be noted that the method of calculating these adjusted indicators could differ from the methods used by other companies.

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