Welcome to an open lecture to learn how to get Medical or In vitro diagnostic medical device innovation to the European Medtech market.
The lecture introduces the MDR and IVDR regulations governing medical devices and in vitro diagnostic medical devices, covering their key requirements, CE marking, and the conditions for market access.
Content is designed for researchers and startups, offers a practical introduction to regulatory requirements and helps participants incorporate regulatory considerations into the product development process from the earliest stages.
Students are also very welcome.
Organiser
IVDR Notified Body SGS Fimko Oy in collaboration with MET faculty