Event Date: 09/05/2022 09:30 - 09/05/2022 13:00
The HPRA will hold a webinar on the In Vitro Diagnostic Medical Devices Regulation (IVDR), covering key topics and providing practical information regarding the application of the IVDR.
The webinar will provide insights into key areas such as national and European implementation of the regulations, post-market surveillance, vigilance and registration requirements, as well as HPRA inspections and performance studies. The final agenda for the webinar will be published on this webpage in the coming days.
The webinar will take place as a virtual event using the Microsoft Teams platform.
Time and date
9.30 am - 1.00 pm, Monday 9 May
Location
The webinar will be hosted virtually using Microsoft Teams.
Who should attend?
IVDR economic operators such as device manufacturers, distributors, importers, authorised representatives, contract research organisations conducting performance studies and persons responsible for regulatory compliance.
Agenda
For information on the presentations included in the webinar, download the agenda.
Registration
To attend, please register in advance by completing our online registration form.
Fee details
The webinar is free to attend and there are no associated fees.