If you are planning to bring a MedTech product to the European market, you have to tackle a regulatory hurdle: the Medical Device Regulation – MDR.

In this workshop, you will learn the why, what, how and when of MDR procedure. Two experts in the field, Willibrord Driessen, independent medical device compliance advisory, and Alex Laan, head of IVD Notified Body will take you through the challenges and opportunities of this traject. We will include the additional challenges with products combining medtech and IVDR, pharmaceutical and/or digital innovations and the effect on your regulatory pathway.

This workshop is organized for all current TTT participants and for other spinoffs from Dutch Knowledge Institutes interested in the topic. We request a short motivation in your application form.

Speakers