Once your order is processed, you will receive a system-generated email and the purchased course(s) will be assigned to your learning plan in the GS1 US Learning Management System (LMS).
The U.S. FDA UDI Rule* sets up a unique device identification system for medical devices. This course is tailored for medical device labelers—such as manufacturers, repackagers, and reprocessors—or anyone involved in implementing UDI. It provides a foundational understanding of specific GS1 Standards that can be used to meet requirements for product identification, product labeling, and submitting information to the U.S. FDA database.