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How to meet Unique Device Identification (UDI) requirements

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The term UDI is used increasingly in healthcare, so understanding what it means and how to meet the regulatory requirements for identification and physical marking of products.

This webinar will provide insight to what UDI means, how to achieve unique device/product identification with GS1 standards and how this can be used not only for international regulatory compliance (US FDA etc.) but also to meet the needs of local industry. Included also are considerations related to your product packaging and options with regards to data carriers (linear and 2D barcodes).


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