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.