Marco de Morpurgo focuses on government regulation of the Life Sciences industry. He helps companies doing business in the EU navigate the complex regulatory structures governing the sector, counseling such clients on regulatory strategies and compliance matters.

His practice covers the regulation of pharmaceuticals, biotechnologies, medical devices, and other health-related regulated products in the EU. He provides strategic advice on a broad range of regulatory issues, including clinical trials, product approvals, market access, promotion and advertising, post-market obligations, as well as on industry-specific ethical and behavioral rules. Most of Marco's work is multi-jurisdictional and he has broad experience assisting clients manage regulatory divergence within the EU and globally.

He regularly speaks and writes on Life Sciences topics. He is a member of the Editorial Board of the European Pharmaceutical Law Review and teaches Life Sciences Law at HEC Paris.