Live Webinar: UDI Compliance in the Real World

by Craig Hodgson, on March 31, 2016

Barcode labeling for UDI ComplianceWhere are you with the FDA’s UDI regulations? With more UDI deadlines fast approaching in the U.S. (as well as new regulations in the works in Europe and elsewhere), medical device manufacturers may need to reevaluate their approach—especially with their barcode labeling—to find a strategy that adapts more easily to regulatory requirements.

During an upcoming webinar on Tuesday, April 5, 2016 at 11:00 AM EDT, GHX and Loftware will share some of the missteps companies have taken in their effort to comply with UDI, and ways you can take an enterprise-wide approach to keep up with evolving requirements.

Karen Conway, CMRP, Executive Director, Industry Relations for GHX, will provide the latest update on UDI compliance including the international impact. Michael Gillespie, Executive Director, North Americas Consulting for GHX, will provide insight into the UDI readiness of your peers, including real-world use cases where compliance was met but at a cost to efficiency and long-term scalability.

To learn more about what you need to do to help ensure short- and long-term UDI compliance, register for next week’s webinar today.

Register for the Webinar

 

 

Topics:Medical DevicesRegulatoryLabeling

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