Are you ready for UDI? Unique Device Identification for medical devices
Add bookmarkThe United States Food and Drug Administration (FDA), the European Commission and other regulators have made safety and integrity of the global Healthcare supply chain a strategic priority by proposing legislation for Unique Device Identification (UDI).
UDI is expected to improve patient safety and Healthcare business processes. A single, global system of standards is fundamental to enable an efficient and effective implementation of UDI by all Healthcare stakeholders worldwide.
By GS1 Healthcare
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