BSI expert talks about the transition to the EU Medical Device Regulations
The new EU Medical Device Regulations will bring major changes to the industry, affecting everyone, manufacturers, notified bodies, competent authorities and the EU Commission.
Understanding and planning your transition to the new regulations is key to ensuring compliance for your medical devices.
Kevin Madden, BSI Medical Device Product Specialist, shares his expertise at Medical Technology Ireland to cover:
- Where are we now?
- Who is responsible?
- What are the key changes?
- The transition period
- Next steps
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.
