BSI expert talks about the changes to the EU MDR and IVDR and the future of the medical device industry
Medical Device manufacturers are facing a number of challenges as a result of the new regulations.
One of the biggest challenges being the sheer workload required to implement the MDR and IVDR and transition from the MDD and IVDD to MDR and IVDR, so understanding the regulations has never been so important.
Watch Kevin Madden, BSI Medical Device Product Specialist, speak about:
- The biggest challenges facing medical device manufacturers in implementing the new MDR and IVDR
- How the new regulations will change the future of the medical device industry
- Other challenges and opportunities that the future medical device industry faces
The Compliance Navigator blog is issued for information only. It does not constitute an official or agreed position of BSI Standards Ltd or of the BSI Notified Body. The views expressed are entirely those of the authors.
