Event Date: 09/11/2020 - 13/11/2020
The HPRA will hold a series of information sessions on medical devices and IVDs from Monday 9 November to Friday 13 November 2020. These sessions will take place from 11 am to 12 pm each day and 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 agenda is now available to download.
To attend the webinars, please register using this link.
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.
There is no fee to attend.