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Beyond Compliance and the FDA Unique Device Identification Rule - How to Achieve Global Standardization

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Managing healthcare information against a backdrop of increasingly complex compliance regulations is far from easy. Savvy organizations are turning to the global standard GS1 to comply with the US Food and Drug Administration (FDA) Unique Device Identification (UDI) Rule.

This brief resource explores what the FDA UDI Rule is, why it was created, and how GS1 standards can be used to achieve compliance. Read on now to learn more.

Vendor:
LANSA
Posted:
20 Feb 2014
Published:
20 Feb 2014
Format:
PDF
Length:
2 Page(s)
Type:
White Paper
Language:
English

This resource is no longer available.