An information day on medical devices and in vitro diagnostic medical devices will be hosted by the Health Products Regulatory Authority (HPRA) on the 23rd May 2018 in the The Galmont Hotel Galway (formerly Radisson Blu Hotel). The objective of the day will be to provide an overview of the implications and interpretation (to the extent possible) of the new EU device regulations for manufacturers and other economic operators.
You can now download the draft Agenda. A final agenda will be made available closer to the event.
Registering for the event is now open. Please use the below links to register for this event.
If you have any queries in relation to the event please contact us by email at email@example.com
HPRA Industry Survey now published
As the negotiations for the UK to leave the European Union continue, the HPRA is asking economic operators to share their views on the potential impact of Brexit on the Medtech sector in Ireland and particularly on the supply chain.
A priority for the HPRA, working with all stakeholders, is to ensure the availability and continued uninterrupted supply of critical use medical devices and in vitro diagnostic medical devices in Ireland.
To complete this short survey please visit the below link.
*The deadline for responses is 8 May 2018