Chantal Benz

Chantal Benz is a Senior Regulatory Affairs Manager at Geistlich Pharma AG, overseeing the EU/EFTA region for Class III medical devices, focusing on a regenerative product portfolio with animal origins. Responsibilities include leading MDR certifications, supporting Notified Body audits, and acting as a process champion in Lean Management. Previous roles include Regulatory Affairs Manager at Zircon Medical, Director of Regulatory Affairs and Quality at Institut Straumann AG, and various positions in regulatory and quality management across multiple organizations. With extensive expertise in medical device regulations, Chantal has been involved in GSPR handling, standard applicability, and the development of labeling and technical documentation. Chantal holds multiple certifications in quality management and regulatory affairs and has a Bachelor's degree in Molecular Life Sciences with a focus on Chemistry.