Maxime Bacrot is an experienced professional in Global Regulatory Affairs with a focus on Immunology and expertise in biological and blood-derived medicinal products. Holding the position of Senior Manager at CSL since January 2024, Maxime has extensive experience in new Marketing Authorization processes, including direct interactions with Health Authorities and thorough preparation of full EU module submissions. Prior to this role, Maxime served as Manager in Global Regulatory Affairs Europe at CSL from February 2018 to December 2023, participating in Pre-MAA Centralized Procedure activities and managing stakeholder communications. Additionally, Maxime held roles at Pierre Fabre as Regulatory Affairs Manager and Project Manager, focusing on OTC products. Educational credentials include a Doctorate in Pharmacy, a Master’s in Biochimie et Biotechnologie, and a Master’s in Regulatory Environment of Health Enterprises, all from esteemed French universities.
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