Navigating Audits, AI Act and MDR: Expert Insights from a Notified Body and Industry
Join us for an exclusive webinar where we dive into critical regulatory topics shaping the future of medical device software and CE-marking.
This session brings together expert insights, including perspectives from Notified Body – BSI, to help you navigate compliance with confidence.
We will cover:
✅ 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
✅ Live Q&A – Ask the experts your burning questions.
- May 22
- 4PM CET
