This practical workshop closes the information gap on the effects of MDR on the approval process of medical devices and accompanies you step-by-step and through practical examples through the entire process of medical device approval.

This practical workshop closes the information gap on the effects of MDR on the approval process of medical devices and accompanies you step-by-step and through practical examples through the entire process of medical device approval.

With the EU MDR, manufacturers must continuously collect clinical data on the performance and safety of their medical devices even after they have been placed on the market. But how do you master PMCF studies in the context of clinical follow-up? In our second informal "MedTech Connect" exchange, it's all about the PMCF phase, which is immensely important in post-market surveillance. Learn what PMCF should ideally look like, under what conditions manufacturers need to conduct PMCF studies, and how they can make these types of studies a success by following simple ground rules. Together with the GKM Society for Therapy Research we offer you an exciting impulse lecture as well as a space to bring your experiences and problems and to exchange ideas.