Advanced Medical Device Regulation Masterclass | Paid Event

This course give you an overall and complete overview about the requirements of the Global Medical Device Regulation. We will discuss the basics about risk classification systems, about the requirements for conformity assessment procedures, about clinical evaluations and trials and about regulatory challenges. The course is very interactive: In Break-Out Groups we will review many examples covering borderline classification products and reports for the market surveillance. Overall you will broaden your experiences in a workshop by exchange with colleagues all over the world.

Host or Publisher GLC Europe