The Eurofins network of companies continues to deliver resilient growth:
€m | FY 2024 | FY 2027 |
Revenues | €7.075bn – €7.175bn | Approaching €10bn |
Adjusted1 EBITDA3 | €1.525bn – €1.575bn | Margin: 24% |
FCFF6 before investment in owned sites9 | €800m - €840m | Approaching €1.5bn |
“I am proud to see that the Eurofins network of laboratories has maintained its solid organic growth track record in Q1 2024, ahead of our objectives. Eurofins teams continue to focus on further implementing programmes related to digitalisation, productivity improvement, pricing and cross-selling initiatives and the ramp up of start-up activities. Despite a challenging geopolitical and macro environment in parts of the world, Eurofins management remains confident in achieving our objectives for the year.”
Eurofins will hold a conference call with analysts and investors today at 15:00 CEST to discuss the results and the performance of Eurofins, as well as its outlook, and will be followed by a questions and answers (Q&A) session.
Table 1: Organic Growth7 Calculation and Revenue Reconciliation
In €m except otherwise stated | |
Q1 2023 reported revenues | 1,574 |
+ 2023 acquisitions - revenue part not consolidated in Q1 2023 at Q1 2023 FX | 27 |
- Q1 2023 revenues of discontinued activities / disposals8 | -16** |
= Q1 2023 pro-forma revenues (at Q1 2023 FX rates) | 1,586 |
+ Q1 2024 FX impact on Q1 2023 pro-forma revenues | -16 |
= Q1 2023 pro-forma revenues (at Q1 2024 FX rates) (a) | 1,570 |
Q1 2024 organic scope* revenues (at Q1 2024 FX rates) (b) | 1,647 |
Q1 2024 organic growth rate (b/a-1) | 4.9%*** |
Q1 2024 acquisitions - revenue part consolidated in Q1 2024 at Q1 2024 FX | 6 |
Q1 2024 revenues of discontinued activities / disposals8 | 0 |
Q1 2024 reported revenues | 1,653 |
* Organic scope consists of all companies that were part of the Group as at 01/01/2024. This corresponds to the 2023 pro-forma scope
** Impacted by discontinuation of the OmniGraf dual-biomarker rejection panel following revised billing guidance by MolDX in the U.S. effective 1 April 2023
*** Impacted by decline in COVID-19 related clinical testing and reagent revenues and not adjusted for public working days (nearly one less day in Q1 2024)
Table 2: Breakdown of Revenue by Operating Segment
€m | Q1 2024 | As % of total | Q1 2023 | As % of total | Y-o-Y variation % | Organic growth7 in the Core Business* | Organic growth7 in the Core Business* adjusted for public working days |
Europe | 850 | 51.4% | 797 | 50.6% | 6.6% | 4.1% | 6.1% |
North America | 628 | 38.0% | 607 | 38.5% | 3.5%** | 7.2% | 7.2% |
Rest of the World | 175 | 10.6% | 170 | 10.8% | 2.5% | 6.9% | 8.8% |
Total | 1,653 | 100% | 1,574 | 100% | 5.0% | 5.5% | 6.8% |
* Excluding COVID-19 related clinical testing and reagent revenues
** Impacted by discontinuation of the OmniGraf dual-biomarker rejection panel following revised billing guidance by MolDX in the U.S. effective 1 April 2023
In Q1 2024, Life (consisting of Food and Feed Testing, Agro Testing and Environment Testing) represented about 40% of Eurofins’ revenues while BioPharma (consisting of BioPharma Services, Agrosciences, Genomics and Forensic Services) represented about 30%, Diagnostic Services and Products (consisting of Clinical Diagnostics Testing and In Vitro Diagnostics (IVD) Solutions) represented about 20% and Consumer and Technology Products Testing (consisting of Consumer Product Testing and Advanced Material Sciences) represented about 10%.
1 Adjusted results – reflect the ongoing performance of the mature10 and recurring activities excluding separately disclosed items2.
2 Separately disclosed items – include one-off costs from integration and reorganisation, discontinued operations, other non-recurring income and costs, temporary losses and other costs related to network expansion, start-ups and new acquisitions undergoing significant restructuring, share-based payment charge4, impairment of goodwill, amortisation of acquired intangible assets and negative goodwill, gains/losses on disposal of businesses and transaction costs related to acquisitions as well as income from reversal of such costs and from unused amounts due for business acquisitions, net finance costs related to borrowing and investing excess cash and one-off financial effects (net of finance income), net finance costs related to hybrid capital and the related tax effects.
3 EBITDA – Earnings before interest, taxes, depreciation and amortisation, share-based payment charge and acquisition-related expenses4, net and gain and loss on disposal of subsidiaries, net.
4 Share-based payment charge and acquisition-related expenses, net – Share-based payment charge, impairment of goodwill, amortisation of acquired intangible assets, negative goodwill, and transaction costs related to acquisitions as well as income from reversal of such costs and from unused amounts due for business acquisitions.
5 Net capex – Purchase, capitalisation of intangible assets, purchase of property, plant and equipment less capex trade payables change of the period and proceeds from disposals of such assets.
6 Free Cash Flow to the Firm (FCFF) – Net cash provided by operating activities, less Net capex5.
7 Organic growth for a given period (Q1, Q2, Q3, Half Year, Nine Months or Full Year) – non-IFRS measure calculating the growth in revenues during that period between 2 successive years for the same scope of businesses using the same exchange rates (of year Y) but excluding discontinued operations.
For the purpose of organic growth calculation for year Y, the relevant scope used is the scope of businesses that have been consolidated in the Group's income statement of the previous financial year (Y-1). Revenue contribution from companies acquired in the course of Y-1 but not consolidated for the full year are adjusted as if they had been consolidated as of 1st January Y-1. All revenues from businesses acquired since 1st January Y are excluded from the calculation. Also, all revenues from discontinued activities / disposals in both the previous financial year (Y-1) and year Y are excluded from the calculation.
8 Discontinued activities / disposals: discontinued operations are a component of the Group’s Core Business or product lines that have been disposed of, or liquidated; or a specific business unit or a branch of a business unit that has been shut down or terminated, and is reported separately from continued operations. For more information, please refer to Note 2.26 of the Consolidated Financial Statements for the year ended 31 December 2023.
9 FCFF before investment in owned sites: FCFF6 less Net capex spent on purchase of land, buildings and investments to purchase, build or modernise owned sites/buildings (excludes laboratory equipment and IT).
10 Mature scope: excludes start-ups and acquisitions in significant restructuring. A business will generally be considered mature when: i) The Group’s systems, structure and processes have been deployed; ii) It has been audited, accredited and qualified and used by the relevant regulatory bodies and the targeted client base; iii) It no longer requires above-average annual capital expenditures, exceptional restructuring or abnormally large costs with respect to current revenues for deploying new Group IT systems. The list of entities classified as mature is reviewed at the beginning of each year and is relevant for the whole year.
For more information, please visit www.eurofins.com or contact:
Investor Relations
Eurofins Scientific SE
Phone: +32 2 766 1620
E-mail: ir@sc.eurofinseu.com
Eurofins is Testing for Life. The Eurofins Scientific S.E. network of independent companies believes that it is a global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
With ca. 62,000 staff across a decentralised and entrepreneurial network of more than 900 laboratories in over 1,000 companies in 62 countries, Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of a wide range of products, as well as providing innovative clinical diagnostic testing services and in-vitro diagnostic products.
Eurofins companies’ broad range of services are important for the health and safety of people and our planet. The ongoing investment to become fully digital and maintain the best network of state-of-the-art laboratories and equipment supports our objective to provide our customers with high-quality services, innovative solutions and accurate results in the best possible turnaround time (TAT). Eurofins companies are well positioned to support clients’ increasingly stringent quality and safety standards and the increasing demands of regulatory authorities as well as the evolving requirements of healthcare practitioners around the world.
The Eurofins network has grown very strongly since its inception and its strategy is to continue expanding its technology portfolio and its geographic reach. Through R&D and acquisitions, its companies draw on the latest developments in the field of biotechnology and analytical chemistry to offer their clients unique analytical solutions.
Shares in Eurofins Scientific S.E. are listed on the Euronext Paris Stock Exchange (ISIN FR0014000MR3, Reuters EUFI.PA, Bloomberg ERF FP).