Get ready for the new EU Medical Device Regulation!
The new Medical Device Regulation (MDR) which becomes fully applicable on May 26, 2021 is initiated to improve patient safety, to increase transparency and traceability but also to bring EU legislation in line with technical advances and create a fair market access for manufacturers.
In the second session in our MDR seminar series, Dr Tina Amini walks you through the details of the MDR requirements when it comes to QMS and the necessary steps to ensure compliance with MDR requirements.
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