Are you ready for UDI? Unique Device Identification for medical devices
We respect your privacy, by submitting this form you agree to having your details passed onto the sponsor who may promote similar products and services related to your area of interest. For further information on how we process and monitor your personal data click here.
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
Have Your Say
Rate this feature and give us your feedback in the comments section below