On the 24th of April 2020, Regulation 2021/561 was adopted and published, delaying the MDR by 1 year to May 26th 2021;
But what did this mean for Medical Device manufacturers?
Our FREE Webinar was to find out and hear about the MDR DELAY EXPLAINED – we covered the impact on:
- Notified Bodies
- Technical Documentation
- EUDAMED & UDI (Unique Device Identification)
- Vigilance & Post Marketing Surveillance
- Person Responsible for Regulatory Compliance (PRRC), Economic Operators and Liability
- Competent Authorities & Sanctions
- And more….
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