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Successful medical device UDI submissions for large portfolios


Successful medical device UDI submissions for large portfolios

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The size of your product portfolio can determine the complexity of your GUDID submission process.

Accuracy and UDI Validation

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As the first deadline for compliance with the U.S. Food and Drug Administration final rule on Unique Device Identification (UDI) swiftly approaches, medical device manufacturers are learning just how vital it is that their UDI data submissions are accurate.