MDR 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 over two decades. So, if you’re planning to sell your devices in Europe in 2021, you need to understand the MDR translation requirements to ensure your organization complies with the regulation and the local legislation of each member state.

Learn everything you need to know about the MDR translation requirements in this webinar presentation produced in partnership with RAPS. Our highly sought after speakers, Mindy McCann and Bob Russell, provide valuable insights about how the current language requirements will change with the upcoming enforcement date. They also outline essential information and detail important process considerations for device manufacturers across the EU, explaining everything you need to do to ensure your multilingual documentation, labeling and quality processes remain compliant under the new regulation. Download the webinar today!

For more information about Morningside’s language solutions for medical device companies, click here.