Webinar: Quality Systems and the MDR Implementation
Topic : Regulation Type : Video
The second in ABHI's series of webinars to introduce the new Medical Devices Regulation. This webinar was developed and presented by Mike Murphy, Mike is QA Director at Coopervision, and a member of the ABHI MDR Implementation WG and Technical Policy Group.
The webinar covers
- Background & Timing of Changes: MDR and ISO 13485
- MDR vs. MDD – Document Comparison
- MDR: Quality Management Systems (QMS) Requirements
- Economic Operators
- ISO 13485:2016 – Key Focal Points and Detailed Analysis of Changes
- Implications & Next Steps