- Services
- EU Regulatory
- Life Sciences
Life Sciences
Our Life Sciences practice combines EU and national regulatory expertise with an understanding of the scientific and commercial issues underpinning our clients’ products and strategies.
Our services
Our team advises major pharmaceutical manufacturers on various regulatory matters relating to the placing of the market of pharmaceutical ingredients under the EU legal framework for human medicines.
We advise manufacturers and retailers of medical devices on the Medical Device Regulation and In Vitro Diagnostic Medical Device Regulation, including scope assessment, monitoring of implementation measures and anticipation of and assistance with compliance of client products and procedures.
Our combined expertise in chemicals, life sciences and food enables us to successfully assist clients with a variety of regulatory issues concerning the identity of so-called ‘borderline products’ at the intersection of distinct pieces of EU legislation, and the correct identification of the regulatory regime under which they belong in order to avoid double or inaccurate regulation of products.
This includes the interplay between medicinal products, medical devices, biocides, cosmetics, detergents, food and food additives.
See full team
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Partner, Chemicals, Products and ESG
Gerard McElwee
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Partner, EU Regulatory, Competition and Trade
Claudio Mereu
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Partner, Chemicals, Products and ESG
Peter Sellar
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Counsel, competition and EU regulatory
Maud Grunchard
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Counsel, EU Regulatory
Natalie Konings
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Associate, EU Regulatory
Aodhan McGourty
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Associate, EU regulatory
Maria-Magdalena Markova
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Associate, EU Regulatory
Chloé Parra
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Brussels, Belgium
- +32 2 742 70 08
- Email Chloé
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Associate
Elise Van Gerven