Podcast: MDR Deadline Countdown | Episode 002: Sufficient Clinical Data

Gert W. Bos, PhD, Fraps
Wiebe Postma, PhD Sr. Clinical Consultant, clinical evaluation, investigation & CRO
Giovanni Di Rienzo

Welcome to our first series: MDR Deadline Countdown,  where we want to guide you as much as possible in your journey towards the MDR. Our host Gert Bos will invite new guest-speakers every episode and discuss topics regarding the MDR. During our second episode, we will talk about sufficient clinical data with a specific focus on legacy products.

Our first guest-speaker is Qserve's  CRO Lead Wiebe Postma. Before Qserve, he obtained his Ph.D. in molecular biology and worked at a large orthopedic manufacturer. 

Also joining us is Qserve’s EU MDR Lead, Giovanni Di Rienzo. Before joining Qserve, he worked at two Major Notified Bodies TÜV Sud and BSI, as well as in the medical device industry.

Want to save our podcast for later? Go to our Spotify channel: Qserve Talks and save our episode!

Do you have any further questions? Feel free to contact us at marketing@qservegroup.com and perhaps we will answer your question in one of our vlogs or podcasts!


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