Navigating Audits, AI Act and MDR: Expert Insights from a Notified Body and Industry
This exclusive webinar provided attendees with insights into critical regulatory topics shaping the future of medical device software and CE-marking.
Check out the Summary of the Webinar: 10 Tips from a Notified Body on MDR, AI Act, Audits and Software tool Validation.
The webinar covered the following topics:
✅ Key considerations & timelines for a CE Conformity Assessment
✅ Best practices for implementing an eQMS
✅ Audit scenarios – what to expect and how to prepare
✅ The latest on the AI Act and its impact on MDR.
