Hélène Rault is a seasoned Regulatory Affairs senior expert with extensive experience in clinical project leadership and regulatory compliance. Previously, Hélène coordinated international phase II and III clinical trials at Servier, contributing to regulatory documents and patient engagement strategies. Currently serving as a Principal Regulatory Affairs Technical Advisor at Medpace, Hélène focuses on medical devices and in vitro diagnostics, ensuring compliance with European guidelines. Hélène holds a Doctor of Pharmacy degree from the Faculté de Pharmacie de Lille and a Master's degree in Life and Health Sciences from Université Droit et Santé Lille II.
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