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

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.

Compliance (Systems Operations) | Compliance Best Practices | Compliance Software | Data Governance | Data Management | FDA | FDA Compliance | Health Care Compliance | Health Care Industry | Information Governance | Information Management | Regulations | Regulatory Compliance | Standards

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