Grégoire Paquet

Associate, Hogan Lovells International LLP

Grégoire Paquet is an associate in the Life Sciences Practice of Hogan Lovells’ Brussels office. A Belgian-qualified lawyer, he assists clients across a wide range of regulatory, legal and procedural matters for pharmaceuticals, biotechnologies, medical devices, and other health-related regulated products in the EU.

He assists companies in the entire lifecycle of products, from early development and design stages, to marketing, and post-marketing issues. His practice also covers a broad array of regulatory questions in EU and Belgian law.

Grégoire has been involved in litigation mandates before the Court of Justice of the European Union, where he leverages his background in EU Law to provide insightful and pragmatic input.

Prior to joining Hogan Lovells, Grégoire was a Pro Bono Lawyer in another international law firm in Brussels.

Contributed to

1

Falsified medicines

Practice notes

This Practice Note explores the changes introduced to the regulation of medicinal products in the EU by the Falsified Medicines Directive to combat the increase in the incidence of falsified medicinal products. First, the Practice Note considers what is meant by the term ‘falsified medicinal product’, before looking at the measures introduced by the Falsified Medicines Directive: greater control of active substances, obligations for actors in the supply chain, the introduction of safety features on the packaging of medicinal products and the common logo for websites selling medicinal products. This Practice Note also provides an overview of the UK regime for falsified medicines.

Life Sciences