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Home » UDI Could Enhance Adverse Event Reporting, Device Tracking, Experts Say
UDI Could Enhance Adverse Event Reporting, Device Tracking, Experts Say
April 5, 2007
Development of unique device identification (UDI), similar to the bar codes on drugs and biological products, could vastly improve the U.S. Food and Drug Administration’s (FDA) ability to respond to adverse events and track recalls, Jeff Crowley, the FDA’s senior adviser for patient safety, said.
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