The healthcare landscape is rapidly evolving, and as it has, the demand for improved patient safety and transparency in medical device usage has become paramount.
In response, global health authorities have established unique device identification (UDI) regulations to provide a standardized approach to how medical devices are identified across healthcare systems worldwide.
This whitepaper examines:
The significance of UDI regulations
Progress in global adoption led by the U.S. Food and Drug Administration
How issuing agencies are supporting medical device manufacturers in complying with these critical standards
Global Unique Device Identification Considerations for Medical Device Manufacturers
1.21 MB
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