- Introduction to UDI requirements
- Device Classifications
- Overview of GUDID key concepts (Review of GUDID Modules)
- The UDI Record
- UDI on Labels, Labeling and Packaging
- Submission and 21 CFR 11 requirements
This webinar on Unique Device Identifier (UDI) requirements will discuss the new rules implemented by FDA. Attendees will get an overview of the new requirement and how to implement.
Dev, MS,CSP, is an international Risk Management and Quality Assurance consultant for Healthcare,medical device, and aerospace industry for over 25 years. He applies evidence base safety techniques from a variety of industries to healthcare. He is a trainer, author of the books Safer Hospital Care, Assurance Technologies Principles and Practices, and Design for Reliability.
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