IMDRF 2023

Christophe Driesmans is graduated as a engineer at KUL Leuven in 2011 and joined the Federal Agency for Medicines and Health Products in 2014 as a medical device evaluator. He is currently leading the vigilance team on medical devices. Christophe represents the Belgian competent authority in various Medical Device Coordination Group subgroups including the one on post market surveillance and vigilance.

Christophe is an expert among the European competent authorities on vigilance and has been involved in many workgroups to improve the vigilance reporting. He is also advising in the development of the European Database on Medical Devices vigilance module.