Getting ready for the EU MDR

In this series of posts, we review the key changes introduced by the upcoming EU Medical Devices Regulation:

  1. Timelines for manufacturers, 14 March 2018
  2. Classification of medical devices, 27 March 2018
  3. Brexit and the medical devices industry: coping with uncertainty, 21 June 2018
  4. Obligations for economic operators, 28 June 2018
  5. New obligations for Notified Bodies, 13 July 2018
  6. Medical devices industry calls for more time to implement EU Medical Devices Regulation, 7 August 2018
  7. Requirements for identification and traceability of medical devices, 20 August 2018
  8. New guidance documents available for manufacturers, 31 August 2018