Training for medical device representatives

Training course/workshop on: Medical Device Adviser (§83 MPDG)

Contents:

• EU legal framework for medical devices and in vitro diagnostic medical devices
• Medical Devices Regulation (MDR) and In Vitro Diagnostics Regulation
• Medical Devices Implementation Act (MPDG)
• Medical Devices Operator Regulation (MPBetreibV)
• How does a product become a medical device/in vitro diagnostic?
• Medical device consultant (MPDG)
• Cooperation with the PRRC (MDR and IVDR)
• Market surveillance/post-market surveillance (MDR and IVDR)

Short biographies of the speakers:

Cornelius 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.