Are you ready for UDI? Unique Device Identification for medical devices
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The 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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