The hidden stings of the Medical Device Regulation (MDR) – Annex VII - eLearning

The Medical Devices Regulation (MDR) is the legislation detailing the requirements that manufacturers must meet to place medical devices on the market in the European Union.

Learn some key requirements about Annex VII of the MDR and gain a better understanding of why notified bodies may be seen to behave differently and in a much more detailed way than what organisations may have previously experienced.

 

How will I benefit?

This course will help you:

  • Appreciate the requirements of Annex VII from the MDR
  • Gain a better understanding of some key Notified Body requirements within the MDR