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AHRMM Comment Letter to FDA Regarding the Draft Guidance for Industry on the Global Unique Device Identification Database (GUDID)November 21, 2013 | Content Areas: Leadership | Tags: Asset Management, Data Standards, UDI | Formats: Comment/Letter/Statement
Comment letter to FDA regarding the draft guidance for industry on the Global Unique Device Identification Database.
November 20, 2012 | Content Areas: Support Services | Tags: Sustainability | Formats: Comment/Letter/Statement
An overview and samples of resources available on the Sustainability Roadmap for Hospitals website.
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-0090November 01, 2012 | Content Areas: Leadership | Tags: CQO, Data Standards, MMIS, Regulatory, Suppliers | Formats: Comment/Letter/Statement
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
May 07, 2012 | Content Areas: Procurement | Tags: Capital Equipment, Distribution, Regulatory | Formats: Comment/Letter/Statement
AHRMM, AHA, FAH, CHA, and HSCA comment letter recommending that the IRS should implement the device tax in a manner that recognizes the 'shared responsibility' commitment from a broad group of key healthcare stakeholders, including medical device companies, to bring forward long-needed national health reform through passage of the Patient Protection and Affordable Care Act ('ACA').
June 14, 2011 | Content Areas: Strategic Planning | Tags: Capital Equipment, Clinical Resource Management, Contracting, Cost Management, Physician Preference | Formats: Comment/Letter/Statement
Leading practice statement on supply chain integration.