European Union in Vitro Diagnostic Device Regulation – EU IVDR
This online course provides comprehensive instruction on the EU IVDR. It covers all aspects of the regulation and identifies key topics and changes, including the economic operators and new roles associated with EU IVDR, standard requirements that must be met by all IVD manufacturers, and pre and postmarket requirements of conformity assessment.
By the end of this course you should be able to:
- Recognize the major changes for the EU in the new IVD Regulation
- Identify key roles associated with the EU IVDR
- Discuss the requirements of the IVD Regulation for key actors
- Explain how to comply with pre and post market requirements for conformity assessment
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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