Resources / WEBINAR

EU MDR Prep: Translation Requirements That Will Make or Break Your Devices In Europe

The upcoming EU Medical Device Regulation (MDR) is the most sweeping change to the EU medical device landscape in two decades; make sure your organization is prepared!

In this webcast hosted by RAPS, you’ll hear from leading medical device regulatory experts who will provide insights about how the current language requirements will change with the upcoming enforcement date. They will outline essential information and considerations for device manufacturers across the EU and explain everything you need to do to ensure your documentation, labeling and quality processes remain compliant under the new regulations.