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.
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