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UID:6a843b141a09f@www.leap-up.com
DTSTAMP:20260818T125932Z
DTSTART:20261111T090000
DTEND:20261111T140000
SUMMARY:Training for medical device representatives
DESCRIPTION:Training course/workshop on: Medical Device Adviser (§83 MPDG)\nContents:\n\nEU legal framework for medical devices and in vitro diagnostic medical devices\nMedical Devices Regulation (MDR) and In Vitro Diagnostics Regulation\nMedical Devices Implementation Act (MPDG)\nMedical Devices Operator Regulation (MPBetreibV)\nHow does a product become a medical device/in vitro diagnostic?\nMedical device consultant (MPDG)\nCooperation with the PRRC (MDR and IVDR)\nMarket surveillance/post-market surveillance (MDR and IVDR)\n\nShort biographies of the speakers:\nCornelius Weber is a qualified healthcare and nursing professional and has successfully completed a bachelor’s degree in medical technology. He is currently undertaking a distance-learning degree in Regulatory Affairs at Lübeck University of Applied Sciences. At the same time\, he supports the regulatory team at leap:up as a working student.
LOCATION:BIO CITY Leipzig\, Deutscher Platz 5\, 04103 Leipzig
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