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Webinar: UDIs in Field Safety Notifications and MHRA Medical Device Alerts

Tuesday 3 December 2019

11:00 AM to 11:45 AM

United Kingdom

Member price: Free

Non-Member price: Free


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.

MHRA logo                     GS1 UK logo

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.

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Who should attend?

This webinar is available for individuals from both NHS trusts and suppliers, that have responsibility for (or are involved in) field safety notifications.

Learning outcomes

From this webinar, you will gain:

  • An overview of UDI and the EU MDR
  • Understanding of the manufacturer recommendations
  • Understanding of provider recommendations
  • Useful resources that you'll be able to refer for guidance

And you'll have the opportunity to ask questions, to help you get the most out of the training.

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