GS1 UDI Training and Advice

Implementation Training and Advice for Unique Device Identification (UDI) for Medical Device Manufacturers and Distributors 

  • Do you require advice and staff training in preparation for compliance with US FDA or EU MDR UDI requirements?
  • Do you understand how to correctly implement GS1 identification numbers on your production lines?
  • Are you aware of the specifications for creating and printing barcode labels?

GS1 experts are on hand to provide you with help needed. We offer both private, company specific tailored courses on your site or optionally you can choose to participate in one of our online webinars to learn about implementing GS1 identification standards such as GTINs and barcodes.

Speak to our Healthcare Sector Experts Siobhain Duggan and Tim Daly or register your interest in UDI Training here.



How to implement Unique Device Identification (UDI) Webinar

The FDA has released the Unique Device Identification (UDI) Rule for medical devices and the E.U. is proposing a similar regulation for medical device marking and barcode labelling within Europe. Both regulations will impact the medical device and life sciences industry in Ireland. This introductory, free-of-charge webinar is designed to introduce manufacturers to the topic and explain the initial steps that need to be taken to prepare for compliance.

GS1 UDI Training and Advice

Advice and training from GS1 experts on implementing GS1 identification standards such as GTINs and barcodes for compliance with UDI requirements.