Getting ready for the EU MDR
In this series of posts, we review the key changes introduced by the upcoming EU Medical Devices Regulation:
- Timelines for manufacturers, 14 March 2018
- Classification of medical devices, 27 March 2018
- Brexit and the medical devices industry: coping with uncertainty, 21 June 2018
- Obligations for economic operators, 28 June 2018
- New obligations for Notified Bodies, 13 July 2018
- Medical devices industry calls for more time to implement EU Medical Devices Regulation, 7 August 2018
- Requirements for identification and traceability of medical devices, 20 August 2018
- New guidance documents available for manufacturers, 31 August 2018