Medical device manufacturers face new challenges when trying to access the European market. Reason for this is the recent publication of the new Medical Device Regulation (MDR). The MDR will have a significant impact on clinical, preclinical and biocompatibility performance as well as other technical requirements.Listen to our presentation on „Implications of the new Medical Device Regulation (MDR) from a product testing and certification perspective“
at the COMPAMED Suppliers Forum.
Find out more about the new regulation and listen our presentation at the COMPAMED Suppliers Forum on Tuesday, November 15, 2016 at 2:15pm in Hall 8b, Booth G40.
Need more detailed information? Then sign up for your personal appointment at our booth E03 in hall 10 at MEDICA to receive a 45min 1-on-1 conversation with our specialists. We'll even get you a free entry ticket code to enter the show and provide you with exclusive access to a "Market Access Q&A" webinar after MEDICA.
Our team of experts is happy to answer any questions on topics such as CE Marking, the EU Medical Device Regulation, Global Market Access and testing of medical devices.
We are looking forward to meeting you!
Exhibitor Data Sheet