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Engineer by training, graduate of the University of Technology of Compiègne, specializing in Biomechanics & Biomaterials, Mathieu Quintin has been working for 20 years in the field of medical devices, with a particular focus on class III devices (invasive devices and implants, especially for the central circulatory system).

He has acquired a varied and complementary experience through positions held at manufacturers (Aesculap BBraun, EuroSurgical), in hospital structures (Research and Innovation Department of the Assistance Publique Hôpitaux de Paris), in clinical CROs (MedPass International) and at the GMED, the only French notified body for medical devices.

These experiences have allowed him to develop a transversal expertise in the fields of regulatory affairs, clinical affairs and quality assurance, as well as a precise understanding of the functioning of the various players in the sector.

He is now Director of Regulatory Affairs at Caranx Medical.