European Union Medical Device Regulation – EU MDR
This online course provides comprehensive instruction on the EU MDR. It covers every aspect of the regulation and identifies key topics and changes, including the economic operators and new roles associated with EU MDR, standard requirements that must be met by all manufacturers regardless of class, and the pre and postmarket requirements of conformity assessment.
By the end of this course you should be able to:
- Recognize the regulatory background in Europe
- Identify the roles associated with the EU MDR
- Discuss the manufacturing requirements of the EU MDR
- Explain how to comply with pre and post market requirements for conformity assessments.
For more information Visit University Website.
Certification / Credits
By completing/passing this course, you will attain the certificate Medical Device Certificate
About NSF International
NSF Health Sciences partners with life science companies, big and small, to provide highly customized end-to-end services throughout the product lifecycle. From early development to commercial manufacture and distribution, our expert services will assist you to: Ensure regulatory compliance Implement...
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