Learn from our experts as they share PMCF successes and failures they've seen so far.

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RQM+ Live! is an interactive live show featuring expert panelists discussing timely topics, challenges, and solutions in the medical device and diagnostics industries. The panelists also answer your questions live! Every episode is added to our podcast, too.

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RQM+_Live_41_Recorded

Your post-market surveillance (PMS) system complying to the EU MDR was put into place in May 2021. How is it going? Now months later, there are an abundance of issues and questions!

This panel discussion provides a unique opportunity to learn from the experiences of seasoned experts as they share PMCF successes and failures they’ve seen across the industry so far. While there have been and will continue to be plenty of implementation challenges, our esteemed panel has worked through comprehensive solutions and is anxious to share.

Discussion will include:

  • Best practices for optimizing PMCF as it relates to the EU MDR implementation
  • Typical NB findings and variations in interpretation
  • Strategies to overcome audit findings and gaps in your evidence

 The panel will include:

  • Amie Smirthwaite, BEng, PhD - Global Vice President, Intelligence & Innovation
  • Nancy J. Morrison, RAC - Executive Director, Regulatory & Quality Consulting Services
  • Jonathan Gimbel, PhD - Executive Director, Technical Leadership, Clinical & Post-Market Practice
  • Celeste Ann Maksim, PhD - Chief of Staff, Clinical & Post-Market Practice
  • Andreas Tarnaris, M.D. MD (Res) FRCS (NeuroSur) - Medical Director

"With partners like you I feel even more confident. I’m very appreciative of how you are presenting both short and long term solutions and speaking your ‘regulatory philosophy’ out loud."

Director, Clinical Compliance, Multinational Medical Device Manufacturer