Geistlich Pharma
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.
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Geistlich Pharma
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Geistlich Pharma AG develops, produces and distributes medical devices and drugs (anti-infectives, vitamins) for regenerative medicine at the Wolhusen and Root sites in central Switzerland. The Swiss company forms part of the Geistlich group which has been in family hands since 1851. Geistlich Pharma and its three business units Geistlich Biomaterials, Geistlich Surgery and Geistlich Medical have ten subsidiaries and global distribution. Some 500 employees work for the company around the world. The company is a world leader in regenerative dentistry through its business unit Geistlich Biomaterials. The ownership structure enables the company to plan long-term and to consistently develop innovative products. Geistlich Pharma AG continuously invests in developing its research and technology and relies on its qualified and specialized employees. Currently Geistlich Pharma is - the global market leader in regenerative dentistry - the leader in biological bone and cartilage regeneration - supplies drugs and medical devices in selected application areas