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FDA Conference Focuses on UDI Rule


The U.S. Food and Drug Administration (FDA) will hold a conference to help medical device manufacturers comply with the Unique Device Identification (UDI) rule, which goes into effect in 2010.

The conference will take place in Orlando, FL, from October 20-21. The conference will give manufacturers an update on the current status of the rule, grasp the fundamentals of an automated identification system, and create a plan for implementation.

The FDA UDI rule was created to establish a single device identification system that is consistent, unambiguous, and standardized.

For more information about the conference, visit http://www.udiconference.com.