The first deadline for the FDA’s Unique Device Identification (UDI) rule has come and gone (September 24, viagra sale 2014). In the past few weeks there have been a number of articles/blogs published with tips for medical device manufacturers on UDI compliance
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. One that I found most interesting was a Fierce Medical Devices interview with Jay Crowley, best viagra former Sr. Adviser for Patient Safety with the FDA’s Center for Devices and Radiological Health (CDRH). Crowley has been referred to as “Mr. UDI” for his central role in developing the UDI system. The article can be found here: