Dear innovator,
Dear researcher,
Are you involved in the development of a medical technologies? Then you don`t want to miss this info session!
What? This info session will give you some insights in the regulatory landscape and procedures that are linked to medical device development, from a notified body’s perspective. It will provide you some guidelines on how to incorporate these regulatory requirements into your research roadmap, also from an early proof of concept phase onwards. You will get the opportunity to ask plenty of questions. The content of the info session is developed in collaboration with HIRUZ (UZ Gent) and a UGent IOF innovation officer.
For Whom? Anyone who wants to know more about the impact of medical device regulation on research developments
When? Thursday December 12th 10h00-12h00
Where? Campus Ardoyen (technologiepark Zwijnaarde), IGent tower, Auditorium 1 (first floor).
Registration? The event is free but registration is mandatory. Register here!