What is EU MDR? | European Medical Device Regulation

Posted by Compliance Quest
5
Apr 7, 2021
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The EU MDR is the European Union Medical Device Regulation 2017/745 released in 2017 by the European Parliament and the Council of the European Union. The intent of the EU MDR regulations is to ensure a high standard of safety and quality for medical devices as well as standardizing data and technological advances through an EU database (EUDAMED).
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