Marie-Eve Charrois

Marie-Eve brings over 20 years of experience in the biopharmaceutical industry, mainly in vaccine development and commercial production. She has served in many roles of increasing responsibility in Regulatory Affairs and Quality. In her most recent position as Site Conformance Manager at GSK Vaccine, she was responsible for supporting the Quebec site in the regulatory strategies for post-approval changes, review, and approval of regulatory submissions. preparation for GMP inspections and their associated Quality Systems. She has spent 18 years at Medicago (a biotech company focused on vaccine development). the five last years as Director of Regulatory Affairs. She played a key role in the preparation of the regulatory dossier to support several Phase 1, 2, and 3 clinical trials conducted in Canada, The USA. Europe, South Africa. and Australia. She has actively participated in formal and technical meetings with regulatory authorities (FDA, Health Canada BRDD, and EMEA) in the context of the vaccine development but also in the context of regulatory interactions associated with the maintenance of licensed vaccines. Marie-Eve owns a Master of Arts from Laval University in Quebec.