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.
In this complimentary on-demand webinar, expert speakers delve into proven strategies and practical solutions to help you navigate these challenges. Learn how to optimize your PMCF process, enhance data quality, and ensure regulatory compliance.
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.
Watch the webinar on-demand below, or download the slide deck.
This webinar is co-hosted with Purdie Pascoe and BSI.