Welcome to AHRMM's Knowledge Center. Find all the resources you’re looking for by applying filters for precise and efficient search functionality.
10 results returned
March 15, 2017 | Formats: Comment/Letter/Statement
On March 6, 2017 House Republican leaders unveiled a legislative package to repeal and replace parts of the Affordable Care Act (ACA). The House Ways & Means and Energy & Commerce Committees, on March 9, completed their work with no amendments to the bills, collectively known as the American Health Care Act. This advocacy alert from AHRMM and the American Hospital Association is asking the field to reinforce our message that coverage must be maintained for the millions of people who could lose it if this legislation becomes law. Please contact your representative and urge him or her not to support the bill when it comes to the House floor for a vote. The bill will be marked up by the House Budget Committee on Thursday, March 16, and the full House could likely vote as early next week.
AHRMM Comment Letter to FDA Regarding the Draft Guidance for Industry on the Global Unique Device Identification Database (GUDID)November 21, 2013 | Content Areas: Leadership | Tags: Asset Management, Data Standards,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Comment letter to FDA regarding the draft guidance for industry on the Global Unique Device Identification Database.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').