This one day workshop is designed for healthcare medical device manufacturers and individuals with front-line responsibility for FDA Unique Device Identification (UDI) and Global Unique Device Identification Database (GUDID). This workshop will focus on the use and implementation of the GS1 Standards including Global Trade Item Number® (GTIN®) and the Global Data Synchronization Network™ (GDSN®) as a method to identify medical devices with a UDI number and bar code and to load the GUDID with device information.
Why attend?
To gain a deep understating of the UDI Rule from Issuing Agency experts. The user will leave the workshop being able to effectively describe what the UDI Rule means and how to use the GS1 Standards for both regulatory and commercial needs of their company. The user will be provided with a directional path forward in relation to the use of GS1 Standards in their UDI work.