Training

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 in preparation for compliance with US FDA UDI requirements.