All medical device manufacturers who want their documentation, labeling or quality processes to remain compliant need to understand the language and translation requirements and implications of the new EU MDR. The overwhelming majority of medical device manufacturers will not be compliant by the May 26, 2020 enforcement deadline. In this webcast, 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 remain compliant. 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.

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

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