Master Ingénierie de la santé – Affaires techniques et réglementation du dispositif médical (M2) at Université Claude Bernard Lyon 1

The field of medical devices is becoming increasingly complex and heavily regulated, requiring experts trained in the latest European and international regulatory frameworks. As this sector continues to grow rapidly, the aim of this programme is to train qualified specialists in medical device regulatory affairs, proficient in both European and global contexts.

Faculty: Polytech Lyon  |  Duration: 4 semesters (2 years)  |  Study mode: full-time; work-study (alternance) route; taught in French  |  Location: Villeurbanne, Auvergne-Rhône-Alpes, France

What you will study

Master the technical and regulatory aspects of medical devices in a broad sense Apply a quality management approach within a hospital technical platform Be capable of implementing the market launch of a new medical device in accordance with the new European regulation Understand and contribute to the management of a medical device company

Career pathways

Technical manager in a company or in a public or private healthcare institution, responsible for the accreditation of medical devices or for the implementation of a quality management system linked to technical platforms. Applications engineer specialising in medical device regulatory affairs.

Official programme page