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).
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AHRMM is offering a repository for leading and proven supply chain practices, case studies, and toolkits that are developed from a
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AHRMM is offering a repository for leading and proven supply chain practices, case studies, and toolkits that are developed from a
Toolkits/Methodology
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