The Official Comment of AHRMM to the United States Department of Health and Human Services Food and Drug Administration (FDA) regarding Unique Device Identification for Medical Devices Docket No. FDA-2011-N-0090
AHRMM comments to the FDA regarding an amendment to the UDI proposed rule to address the UDI implementation time frame required by the 2012 Food and Drug Administration Safety and Innovation Act (FDASIA).
Related Resources
Webcast
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.
Webcast
In part one, we explore the reasons why the FDA created the (UOU) Unit of Use.
Supply Chain Strategies & Solutions Article
By: Mike Berger
Supply Chain Strategies & Solutions Article
From a supply chain perspective, the use of UDIs will help with the visibility of supplies throughout the continuum of care.
Supply Chain Strategies & Solutions Article
By: Richard Bagley
Supply Chain Strategies & Solutions Article
Millennials will continue to remain significant to the growth of healthcare in years to come.