Creating a Strategic Foundation of Quality Data
Siemens Healthineers takes UDI implementation to next level for its digital transformation
Using compliance with the U.S. Food and Drug Administration (FDA) Unique Device Identification (UDI) Rule as the spark, Siemens Healthineers ignited systemic data governance, data quality, and data collaboration programs and processes that promise a future continuum of value.*
Interested in learning more about data quality?
Check out our other resources to help you share and synchronize trusted data
- Best Practice Guide for Sharing Vital Attributes in Healthcare
- Creating the Case for Trusted Data PDF (573 KB)
- Getting Started with the GS1 Global Data Synchronization Network (GDSN) PDF (1.36 MB)
- QuickStart Guide for implementing the GS1 Global Data Synchronization Network (GDSN) in Healthcare PDF (419 KB)
*For information about the rule, see the U.S. FDA Unique Device Identification System
Disclaimer: GS1 US is the local GS1 Member Organization that supports implementation of the GS1 System in the United States. GS1 US employees are not representatives or agents of the U.S. FDA, and the content herein has not been reviewed, approved, or authorized by the U.S. FDA.
GS1 is a U.S. FDA-Accredited Issuing Agency for UDI, and GS1 Standards are authorized for use in implementing the requirements of the U.S. FDA UDI Rule.