Diane de Michelena

Diane De Michelena is an experienced professional in regulatory affairs with a focus on rare diseases and international registration processes. Currently serving as an R&D EU Regulatory Affairs Project Manager at Laboratoires Théa since September 2024, Diane previously held positions such as Regulatory Affairs Manager at Advicenne, where responsibilities included managing the EMA centralized procedure and registrations in the Middle East. Notable past roles include Regulatory Affairs Project Manager at Unither Pharmaceuticals, where Diane worked on the European Decentralized Procedure, and International Regulatory Affairs Manager for the Onco project at Pierre Fabre Group, handling registrations in Brazil and Mexico. Diane's expertise extends to consulting for companies like Sobi and Sanofi in various regional projects, complemented by a Doctor of Pharmacy degree from Université d'Auvergne, focused on vaccination and public policy in Latin America.