European Union Medical Device Regulation – EU MDR

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.

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 helpful for all medical device professionals, management and executive personnel looking to expand their knowledge of the EU MDR.

By completing/passing this EU MDR course, you will attain the Medical Device Certificate.