Implementation of MDR 2017/745 in Belgium

In this half-day training, we will zoom in on processes and legislative guidance documents implementing the MDR 2017/745 in Belgium. 

The course consists of 3 parts, covering translational aspects, submissions, and reporting of clinical investigations in Belgium: You will learn how submission for approval of clinical investigations works and finally, you will learn how reporting of your investigation (safety reports and study reports) works in Belgium.

For more information: click here.