The MDR, in application in Europe since May 2021, is one of the strictest and most complex regulatory systems for medical devices in the world. For that reason you can not start early enough to become EUDAMED ready. From attribute analysis to testing services and data transfer: in this webinar we will show you how to cope with this major challenge efficiently and without any risk.
Take 2 minutes to find the optimal solution for the registration of your medical devices.
You want to register your medical devices in a national UDI database like EUDAMED or GUDID (FDA) or share them with business partners worldwide, but d...