Unique Device Identification (UDI): Regulation & Compliance 101

Your label is your product. As the FDA begins enforcing Unique Device Identification (UDI) labeling requirements, it is crucial for medical device manufacturers, distributors, and end users to be current with regulations to ensure compliance. This session will provide valuable insights and best practices for meeting UDI labeling requirements, covering topics such as the importance of proper UDI marking verification, effective labeling strategies, and the significance of traceability in ensuring patient safety. By attending this webinar, participants will gain the knowledge and tools necessary to navigate the UDI mandate successfully, optimize their labeling processes, and ensure compliance with FDA regulations.