Material Detail

EU-MDR

EU-MDR

EU MDR (The European Union Medical Device Regulation) is a regulatory framework that applies to all European medical device manufacturers to establish high quality and safety standards for medical devices production.

refer:   ...

Show More

Quality

  • User Rating
  • Comments
  • Learning Exercises
  • Bookmark Collections
  • Course ePortfolios
  • Accessibility Info

More about this material

Comments

Log in to participate in the discussions or sign up if you are not already a MERLOT member.