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New Whitepaper by BSI and Eclevar on EU MDR – Download Now!

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.