MDR/IVDR - Economic operator obligations, Eudamed and national registration requirements

This webinar was part of a HPRA Medical Devices webinars series held in November 2020 to provide information about the Medical Device Regulation (MDR) and the In Vitro Diagnostics Regulation (IVDR).
This webinar presentation covers two topics.
2:33 Andrew Dullea provides a practical overview of economic operator obligations and responsibilities within the supply chain under the MDR. This presentation will focus on Articles 13 and 14 of the MDR.
27:15 Andrea Hanson provides an update on Eudamed’s development and national registration requirements.