Jay Crowley, Senior Advisor for Patient Safety in FDA’s Center for Devices and Radiological Health, hosts a webcast on the FDA’s Unique Device Identification System proposed regulation. The webcast describes how the anticipate the UDI system is going to work, how the UDI system will affect device manufacturers, and the products that are exempt from UDI labeling.
Medical device manufacturers will want to view the webcast to keep abreast of what is happening with the FDA-mandated identification system.
If you want to download a PDF file of the slides from the webcast, go to the FDA site here.
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