FDA on track with UDI draft regulation
This article was originally published in Clinica
The US FDA draft 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 its main architects. Jay Crowley, senior advisor for patient safety at the FDA’s Center for Devices and Radiological Health, has said that the final regulation would come into force around a year later.
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