We’re thrilled to announce that Eclevar has collaborated with BSI to publish a comprehensive whitepaper: “EU MDR – Post Market Clinical Follow-Up: Gaining Real-world Evidence Challenges and Solutions”.
🔍 In this whitepaper, you’ll find detailed insights on:
- Definitions of PMCF activities under MDR
- Setting up and maintaining a Post-Market Surveillance (PMS) System
- Understanding the requirements and guidance from the latest regulations
💡 Why download our whitepaper?
- Gain a thorough understanding of PMCF activities
- Learn how to enhance your PMS system effectively
- Discover strategies to perform better, reduce risk, and foster excellence in your organization
Don’t miss out on this valuable resource! Click the link below to download and start leveraging real-world evidence for your medical devices.
