Clinical evidence for CE marking of medical devices and IVD devices according to new MDR and IVDR

Join PCG Clinical Services and QAdvis for a half-day Medical Device seminar!

The seminar will outline the new Medical Device Regulations (MDR 2017/745) and in-vitro Diagnostic Regulations (IVDR 2017/746) that will come in effect over the next two to four years. PCG and QAdvis will present strategies and opportunities to navigate through these new requirements. The seminar will explore clinical evaluation and clinical performance evaluation regulations as well as clinical investigation techniques for both before and after CE-marking.

Read more and register here!

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