2017 UDI Conference
June 7, 2017 - Baltimore MD US
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.
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