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An Important Look at the Proposed Unique Device Identification Regulation

Overview: The webinar will explain FDA’s proposed regulation on the Unique Device Identification System. UDI will require most device manufacturers to apply a unique code to their devices and submit data to FDA’s Global Unique Device Identification Database. The webinar will also describe the uses of UDI to improve healthcare.

Speaker: Jay Crowley, Senior Advisor for Patient Safety, FDA’s Center for Devices and Radiological Health

Cost: Complimentary – AHRMM Members; $99 per recording – AHRMM Non-members

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This webinar was recorded on December 13, 2011.

Biography
Jay Crowley is Senior Advisor for Patient Safety, in FDA’s Center for Devices and Radiological Health. He is interested in developing and implementing new methods and techniques for identifying and resolving problems with the use of medical devices. Crowley has held variety of positions over his 20+ years at FDA. Currently, Crowley has primary responsibility for implementing the Unique Device Identification System requirements of the 2007 FDA Amendments Act. He holds a master’s degree in risk analysis and a bachelor’s degree in mechanical engineering.