The FDA UDI Regulation establishes a single device identification system that is consistent, unambiguous, standardized, and globally harmonized. All manufacturers of medical devices will be required to comply with the new UDI methodology. The annual UDI Conference is the ONLY event dedicated to guidance and training for those impacted by the UDI Regulation.
The UDI Conference is specifically structured for implantable, life-supporting, and life-sustaining devices and Class II medical devices facing imminent compliance dates, as well as hospitals moving towards incorporating UDI data into existing systems.
Learn how device manufacturers, distributors, and hospitals will be able to facilitate the following with a UDI system:
The UDI Conference attracts medical device manufacturers, distributors, GPO’s, and hospital systems that are impacted by the regulation.