Articles
Cost, Quality and Outcomes (CQO) Movement, Data Standards, Materials Management Information System (MMIS), Regulations and Regulatory Advocacy, Suppliers, Leadership
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
By AHRMM
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).
Capital Equipment, Products and Services Contracting, Suppliers, Procurement
Furnishing, Installation of Furniture, Equipment RFP
By WellSpan Health, AHRMM
Sample furnishing, installation of furniture, and equipment sample request for proposal.
Capital Equipment, Distribution, Regulations and Regulatory Advocacy, Procurement
IRS Issues Final Rule Implementing Medical Device Excise Tax
An announcement of the Final Rule issued by the IRS.
Capital Equipment, Products and Services Contracting, Cost Management, Financial Management, Reprocessing Medical Devices, Leadership
Navigating the Economic Storm: A Prescriptive Approach for Healthcare Supply Chain Professionals
By AHRMM
In this page, AHRMM recommends these 3 proactive activities in the event of economic downturn.
Change Management, Clinical Resource Management (CRM), Legislation and Legislative Advocacy, Regulations and Regulatory Advocacy, Performance Metrics
Recent Guidance on Meaningful Use of EHRs Makes Compliance More Difficult
Recent Guidance on Meaningful Use of EHRs Makes Compliance More Difficult.
Asset Management, Capital Equipment, Products and Services Contracting, Purchased Services, Strategic Sourcing, Strategic Planning
Generic Reference Lab RFP
By AHRMM
A sample of generic reference lab request for proposal.
Pharmacy, Suppliers, Logistics
IV Strategies for Disruptions - How to Guide
By AHRMM
How-to guide to managing IV disruptions.
Benchmarking, Products and Services Contracting, Distribution, Financial Management, Lean/Six Sigma, Strategic Planning
Global Unique Device Identification Database (GUDID) Draft Guidance for Industry
By Center for Devices and Radiological Health, Informatics Staff, U.S. Department of Health and Human Services Food and Drug Administration, AHRMM
This page provides information about submitting data to the database for device Labelers, entities responsible for providing the data to the GUDID.
Data Standards, Financial Management, Materials Management Information System (MMIS), Regulations and Regulatory Advocacy, Medical Device Technology
Guidance on Humidity Levels in the Operating Room
By AHRMM
New Guidance on Humidity Levels in the Operating Room