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US FDA on track with UDI draft regulation

This article was originally published in SRA

Executive Summary

A draft US Food and Drug Administration regulation governing the use of unique device identifiers (UDIs) on medical products is on schedule to be published by the middle of 2010, according to one of the main architects of the project. The final regulation would come into force around a year later, Jay Crowley, senior advisor for patient safety at the FDA’s Center for Devices and Radiological Health, said in an interview with RAJ Devices.

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