The first Unique Device Identification (UDI) compliance deadline for medical devices is two months away. Medical device manufacturers still have many questions about compliance. This webinar will provide answers to the most common UDI and Global UDI Database (GUDID) questions.
Questions will be answered by Jay Crowley, Vice President of UDI Solutions and Services at USDM Life Sciences. Jay developed the framework and authored key requirements for the FDA’s UDI system. He was Senior Advisor for Patient Safety in the Food and Drug Administration’s Center for Devices and Radiological Health.
The discussion will include:
- Overview of UDI compliance deadlines (class III,II,I)
- Answers to top UDI compliance questions
- Q & A session: answers to your UDI questions