Join us to Decode CER’s Impact on Medical Devices and Master the Art of Choosing Effective PMCF Strategies.
Starting with an introduction to Clinical Evaluation Report (CER) our experts will guide you through its implications on medical device development, deployment, and post-market surveillance.
The second part of our webinar will focus on unraveling the intricacies of Post-Market Clinical Follow-up (PMCF) strategies. We provide clear, actionable guidance on how to choose the most effective methods for comprehensive data collection over the entire lifetime of a medical device.
Whether you’re new to the field or a expert professional looking to keep abreast of the latest trends and regulatory requirements, our discussion promises to enhance your understanding and arm you with strategies for success. Don’t miss this opportunity to stay ahead in the evolving landscape of medical device regulation and technology.
✅ Discover how to select the optimal Post-Market Clinical Follow-up (PMCF) strategies for comprehensive lifetime data collection.
✅ Gain insights into the best methods for data collection and implementation to ensure regulatory compliance.
✅ Learn how to leverage PMCF strategies to improve device performance and enhance patient outcomes.
Date/Time: July 28 Time 4pm CET