Marie Stutzmann

Senior Associate

Marie Stutzmann is a biomedical engineer with a specialization in regulatory affairs for medical devices. She has over 5 years of experience working in different medical device companies. She has been in charge of the redaction of clinical and biological evaluation reports, and also worked as a toxicological regulatory expert at a major French medical device company. In this role, she provided support during the design and development of various medical devices, including the evaluation of the impact of change on biological safety, redaction of toxicological risk assessments, and biological evaluation reports. At Medidee, Marie provides clients with strategic and assessment support related to the biological safety of medical devices, as well as any other request related to biocompatibility and biological requirements, covering the full product life cycle. Marie speaks fluently French and English, with extensive knowledge of German.