Elevate your clinical evidence to Rank 4 in hierarchy for EU MDR compliance

This webinar hosted by Cetas Healthcare, brought together experts from multiple domains of the EU MDR to provide practical insights on clinical data.

In case you were unable to attend the webinar, we want to make sure you still have access to the valuable insights that were shared during the live session. Therefore, we are happy to share the recording link or answer any questions you may have on PMCF Surveys in a free 30-minute session with one of our speakers.

Objectives

1. Gain an understanding of the clinical evaluation process in the post-market phase of the device
2. Learn how to define and plan appropriate strategies to meet requirements under the EU MDR
3. Hear our experts’ experiences to date from multiple manufacturers
4. Know more about the challenges other manufacturers may face and possible solutions
5. Get an insight into the tips, tricks, and pitfalls of PMS and PMCF under the EU MDR
6. Solve hypothetical case studies and benefit from an extended Q&A session

Check out this video snippet from the live webinar, and if you want to hear more, simply connect with us.

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Speakers

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Objectives

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Speakers

Sumit Mehta

Rachel Derksen

Prem Pandey

Raghavan Ramachandran Nurani

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