Maud Target

Maud Target is an experienced regulatory affairs professional with a comprehensive background in pharmaceutical and vaccine regulatory processes. Currently serving as a Senior Regulatory Affairs Officer at Laboratoire Aguettant since May 2022, Maud has previously held roles such as Regulatory Product Manager at Sanofi Pasteur and Regulatory Project Manager at Substipharm, where responsibilities included the preparation and submission of various regulatory documents, regulatory support for European clients, and lifecycle management. With extensive experience in both European and international regulatory environments, Maud has demonstrated expertise in managing marketing authorization applications, responding to health authorities, and developing regulatory strategies across multiple regions. Maud holds a Master's Degree in Pharmaceutical Engineering with a focus on Translational Pharmacology and has diverse experience in clinical research and technical writing.