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Medical Device Clinical Evidence Event

Welcome to our Medical Device Clinical Evidence Event

Clinical evidence for CE marking of medical devices and IVD devices according to new MDR and IVDR – Requirements and possibilities!

Join PCG Clinical Services and QAdvis at this very special half-day Medical Device seminar followed by a lunch mingle in Medicon Village on March 23rd. The seminar will outline the new Medical Device Regulations (MDR 2017/745) and in-vitroDiagnostic Regulations (IVDR 2017/746) that will come into effect over the next two to four years. PCG and QAdvis will on the basis of these new regulations present strategies and possibilities to navigate through these requirements. It involves clinical evaluation and clinical performance evaluation regulations as well as clinical investigation techniques involving products both before and after CE-marking.

QAdvis is a long time trusted provider of medical device regulatory services and PCG Clinical Services is a full-service CRO committed to improving clinical investigations through our scientific expertise, progressive technology and more effective ways of working.

Presentations and Q&A are verbally held in Swedish. View our agenda and register before seats run out!


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