Event Date: 09/11/2020 - 13/11/2020
The HPRA held a series of information sessions on medical devices and IVDs from Monday 9 November to Friday 13 November 2020. These sessions took place from 11 am to 12 pm each day and were made available via webinar.
The webinar series aimed to provide insight into some of the practical application of the Medical Device Regulation (MDR) and the In vitro Diagnostics Regulation (IVDR) requirements in the areas of economic operator obligations, remote inspections, EUDAMED and registration, clinical data and IVDs.
Webinar Recordings
The webinar recordings and the presentation slides are now available to view.
Agenda
The agenda is now available to download.
Aim of the Webinars
The key objective was to provide an overview of some of the practical considerations for implementation of the MDR and the IVDR.
Who Should Attend
Medical device and IVD economic operators, including manufacturers and distributors.
Fee Details
There is no fee to attend.