Marco Morpurgo

Marco de Morpurgo deals with all the regulatory aspects concerning the Life Sciences sector. With extensive and significant international experience in the sector, he regularly advises clients on multi-jurisdictional projects of European and global reach.

Qualified in various legal systems in Europe and in the United States, in the last 12 years he has practiced in Brussels, London, Paris and Rome.

He advises established and emerging companies operating in the pharmaceutical, biotechnology and medical device sectors in the European Union, as well as service operators in the sector interested in internalising their activities.

Marco helps clients navigate the complex and articulated regulatory framework that governs the sector by offering strategic and compliance consultancy activities in multiple areas - R&D, product classifications and any authorizations, regulatory incentives, market access, promotion and advertising, as well as the specific ethical principles that concern this industrial sector.

In his role as Co-Chair of the firm's Life Sciences practice globally, Marco leads and coordinates a legal team of more than 300 attorneys who assist clients operating in over 40 jurisdictions worldwide, providing them with innovative solutions.

He is a member of the editorial board of the European Health & Pharmaceutical Law Review, teaches Life Sciences Law at the HEC in Paris.