European Union Medical Device Regulation (EU MDR) (2 hours)
5
What you'll gain from this course
Learn anytime on any device
Interactive modules and knowledge checks
Certificate available upon completion
This two-hour self-paced course provides comprehensive instruction on the European Union Medical Device Regulation. It covers every aspect of the regulation and identifies key topics and changes, including economic operators and new roles associated with the EU MDR, standard requirements that must be met by all manufacturers regardless of class, and the pre- and post-market requirements of conformity assessment.
Key learning objectives:
By the end of this course, you will 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
NSF’s EU MDR training is
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