Anne Charpentier, PhD

As a Director at Voisin Consulting Life Sciences (VCLS), Anne works in close collaboration with life science companies to provide strategic input and regulatory writing services to support MAA submissions and lifecycle management activities of innovative drugs and biologics.

She brings to the position more than 20 years of experience, from working in the Pharmaceutical Industry and in a Contract Research Organization (CRO), where she gained an in-depth knowledge of various therapeutic areas and product types (e.g. oncology, neurology, ophthalmology, narcotics, generics and OTC products).

Anne started her career as a Regulatory Affairs Project Coordinator at Sanofi where she was responsible for coordinating the labelling activity between the supply chain and affiliates in non-EU countries.

She then worked as Regulatory Affairs Area Coordinator at Ethypharm, where she was in charge of Marketing Authorization Applications (national, MRP and DCP), license maintenance activities, and liaison with regulatory agencies on behalf of clients located in the EU.

Anne was subsequently employed by a CRO (IQVIA), providing regulatory consultancy services. There, she was responsible for compiling and filing initial EU Marketing Authorization Applications and conducting Life Cycle Management activities, as well as performing compliance review on EU dossiers. She was also responsible for defining strategy and coordinating the registration of Clinical Trial Applications, working closely with the French regulatory agency, the ANSM.

Prior to joining VCLS, Anne worked as Regulatory Affairs Senior Manager at Medis, where she led a team of 3 regulatory affairs specialists. The role involved working in close collaboration with cross-functional internal teams and French clients, and acting as a key liaison person for all regulatory activities. She was responsible for building the registration plan and ensuring the launch of products at patent expiry date for generics products, preparing and submitting Marketing Authorization Applications, and in the writing and review of the responses to regulatory agency’s questions to facilitate the granting of a product license.

Anne graduated in 2000 with a Pharm. D. from the University of Caen, France, and in 2001 with a M.Sc. in Health Law from the University of Sceaux, Paris, France.

In addition to French, her mother tongue, Anne speaks English, and has basic knowledge of Spanish and Greek.

Anne is based in our Boulogne office in France.