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 2017 UDI Conference will focus on UDI adoption and implementation as well as data quality and data management.
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.