Tuesday 3 December 2019
11:00 AM to 11:45 AM
Unique Device Identification is already a requirement of the US FDA, the NHS in England and of the EU Medical Device Regulations.
These requirements are already being met by most medical device manufacturers using GS1 standards. And some manufacturers are already including these UDIs in Field Safety Notifications (FSNs) and subsequently MHRA Medical Device Alerts.
This is vital to improve the speed and accuracy of product recalls by healthcare providers.
Join the MHRA and GS1 UK on this webinar to find out how making a few simple additions to your notifications can improve patient safety. You'll wonder why you haven't done it sooner.
This webinar is available for individuals from both NHS trusts and suppliers, that have responsibility for (or are involved in) field safety notifications.
From this webinar, you will gain:
And you'll have the opportunity to ask questions, to help you get the most out of the training.