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The FDA UDI Rule will establish a single device identification system that is consistent, unambiguous, standardized, and globally harmonized. All manufacturers of medical devices will be required to comply with the new UDI methodology. Attend the Conference to: receive an update from the FDA on current status of the UDI Rule;  grasp the fundamentals of an automated identification system; understand the why's, how's & the “"what's in it for me"; create your plan for implementation; get a jump-start in advance of the UDI Rule for a smooth transition; learn how to guide your organization through the UDI Rule. Go to www.udiconference.com/ for more info.

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