Max graduated from the University of Vermont’s School of Business Administration with a concentration in Marketing and Chemistry. Max enjoys playing live music, cooking with style and launching products for a better world.
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FDA's proposed regulation to set up Unique Device Identifiers scheduled for a seven-year phase-in to minimize burdens on regulated businesses.
Labels for many medical devices will need to contain "unique device identifiers" (UDIs) to help aid with corrections and recalls and to help thwart counterfeiters. The UDI willd be featured in in both plain text format and readable tech form (automatic identification and data capture, "AIDC").
The U.S. Food and Drug Administration issued a proposed regulation to set up the UDI system in early July, and the public has a chance to comment on the proposal until Nov. 7 of this year.
For more information: Healthcare Packaging
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