Collecting Clinical Data through Post-Market Clinical Follow-up (PMCF) activities is an essential component in monitoring the safety and performance profile of your Medical Device under the EU MDR. However, gathering reliable post-market clinical data is complex and presents medical device manufacturers with unique challenges.
Whether you're new to PMCF or looking to refine your approach, this webinar is designed to provide actionable insights to help you achieve success in your PMCF activities. Don’t miss this opportunity to stay ahead of the curve and ensure your medical devices meet the highest standards of safety and performance.
Download the PPT here, or watch the webinar on-demand.
This webinar is co-hosted with Purdie Pascoe and BSI.