Medical Device Regulatory Framework (MDR & IVDR)

The presentation focuses on key definitions and scope of MDR/IVDR, the classification of medical devices and the validity of certificates. Enrich your knowledge around the “”Medical Devices as a Software”” topic and economic operator obligations under the MDR/IVDR and understand concepts such as UDI, EUDAMED and notified bodies.

Target audience: Economic operators from the entire supply chain (from manufacturer to distributor) and, in particular, researchers, executives of medical technology products, startups, and IT companies active in the field of medical applications regardless of department and specialization.