Overview

Marc provides cutting edge strategic and regulatory advice to life sciences clients and represents them in litigation.

Marc is the Co-Head of our International Life Sciences and Healthcare group and head of our Regulatory, Public and Administrative Law Group in Brussels

Specialising in life sciences, he provides both contentious and non-contentious strategic advice to Belgian and international pharmaceutical, biotech and medical devices companies as well as national and European industry associations facing complex regulatory frameworks. Marc's areas of expertise cover issues relating to life-cycle management, clinical trials and data, data exclusivity, marketing, price and reimbursement authorisations, e-health together with distribution and advertising issues. He advises numerous biotech companies on a wide range of issues regarding Advanced Therapy Medicinal Products as well as the legal and bioethical issues relating to research and/or the use of human cells and tissues.

His expertise also covers a full range of public procurement and related litigation, environmental law, REACH, RoHS, WEES and other Belgian and EU regulatory compliance issues. He advises companies, public bodies and industry associations on related matters.

Marc holds a law degree from the Vrije Universiteit Brussel (VUB) where he  worked for four years as a research assistant, and a degree in public and administrative law from the University of Brussels (ULB). Before joining us, Marc was an expert adviser to  the Vice-Prime Minister of Belgium for three years.

Marc regularly publishes and speaks on life sciences regulatory topics and provides an introduction to Biotech Law at the VUB. He is also member of the Board of the Belgian Biotech sector organisation BIO.BE.

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