Event Date: 09/11/2020 – 13/11/2020
The Health Products Regulatory Authority (HPRA) will hold a series of information sessions on medical devices and IVDs from Monday 9 November 2020 to Friday 13 November. These sessions will be made available via webinar.
The webinar series will 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.
The full schedule of webinars can be viewed here.
While the webinars are free, you must book in advance on HPRA website
Aim of the Webinars
The key objective is 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.
All webinars are free