UDI and Providers: What You Need to Do

By AHRMM

Get the basics on what healthcare supply chain and manufacturers, together with clinical and IT departments, must do to implement the Unique Device Identifier and adverse event reporting, and the subsequent effects that will trickle-down to individual patients and the global health population.

Related Resources

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A UDI Capture Work Group Case Study at the Baptist Health.
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In part one, we explore the reasons why the FDA created the (UOU) Unit of Use.
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In the third part of the the FDA Unique Device Identification (UDI) “Unit of Use” (UOU) webcast series, we cover several potential use cases for th
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In part two of the FDA Unique Device Identification (UDI) Unit of Use (UOU) webcast series, we cover the FDA definition of the term, Unit of Use.
Case Studies
WORK GROUP TITLE: UDI Capture Work Group CASE STUDY PARTICIPANTS: