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Recent Guidance on Meaningful Use of EHRs Makes Compliance More Difficult

Letter/Comment
Recent Guidance on Meaningful Use of EHRs Makes Compliance More Difficult.

AHRMM Comment Letter to FDA Regarding the Draft Guidance for Industry on the Global Unique Device Identification Database (GUDID)

Letter/Comment
On November 21, 2013, AHRMM submitted electronically

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

Letter/Comment
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 A

Global Unique Device Identification Database (GUDID) Draft Guidance for Industry

Letter/Comment
This page provides information about submitting data to the database for device Labelers, entities responsible for providing the data to the GUDID.

AHRMM Statement on Comparative Effectiveness

Letter/Comment
AHRMM supports the concept and use of Comparative Effectiveness Research (CER) to provide evidence-based data to help inform purchasing decisions.