Clément CHAUMONT

Clément Chaumont, PhD, is a Senior Regulatory Affairs Specialist with extensive experience in regulatory operations for medical devices. They held roles at Clariance Spine as both a Regulatory Affairs Engineer and Leader, contributing to CE marking and FDA submissions, and have supported compliance with EU MDR requirements. Clément has also worked as a Regulatory Affairs Associate at Cochlear and has a strong academic background, including a PhD in Chemistry from Université de Strasbourg, where they also obtained multiple degrees with honors in relevant fields.