Search Results
The default setting for search results displays All Content. If you prefer to see recent content only, please adjust the date filter.
Filter your results:
Types
Topics
76 Results Found
UDI Impacts on Recall Management Work Group Report
The UDI Impacts on Recall Management Work Group, a part of AHRMM's Learning UDI Community (LUC), has released their recommended practices reports that analyzes the barriers and highlights the benefits to patient safety and key stakeholder groups when utilizing the UDI throughout the recall process. Work group members identified recommended practices for each of these groups underscoring mutual areas for improvement in the safety and efficacy of the recall process.
In addition to the two Impact Reports, there is also a comprehensive Regulatory Resource Guide and a Supporting Information document with detailed reports, resource links, surveys and summary presentations that the work group members created, as well as a Recall Time & Cost Collection Tool.
Connected Care: Challenges and Opportunities to Improve Workflow and Enable Better Patient Care
The proliferation of new bedside medical devices and other system and technologies, including EHRs, smartphones, secure texting apps and more, has added new demands on nurses in the hospital. That demand has only intensified since the onset of the COVID-19 pandemic.
Multiple Device Identifier Work Group Report
Guides/Reports
This downloadable report reviews the recommended practices related to the allocation of multiple unique device indicators (UDI-DI).
In Partnership with AHRMM, Institute for Supply Management® Expands Portfolio of Economic Reports with Launch of Hospital PMI™
CHICAGO, July 23, 2020 — In partnership with the Association for Health Care Resource & Materials Management (AHRMM) of the American Hospital Association, Institute for Supply Management (ISM)
Nebraska Medicine Targets Earlier Diabetic Retinopathy Detection with AI
Nebraska Medicine, based in Omaha, Nebraska, however, has begun testing an AI tool in two of its primary care clinics to detect diabetic retinopathy in patients — a condition that can lead to blindness.
The Critical Link Between Cost, Quality, and Outcomes (CQO) and Unique Device Identification (UDI) White Paper
White Papers
In an effort to capture broader insights on UDI adoption from across the health care field, AHRMM, with participation by the FDA, held LUC Data Quality Workshops during four conferences in 201
7 Innovative Devices from CES 2024 Could Reshape Patient Self-Care
The recent CES 2024 show (formerly the Consumer Electronics Show) produced a number of health care-related, attention-getting devices. Some are not commercially available yet, but these products have the potential to help patients take greater control of their health.
GAO recommends FDA, CISA update medical device security documentation based on AHA input
The Government Accountability Office Dec. 21 recommended the Food and Drug Administration and Cybersecurity and Infrastructure and Security Agency update a 5-year-old agreement regarding medical device security.
Report offers ways to address cybersecurity challenges posed by legacy medical devices
The Food and Drug Administration on Nov. 16 announced a new report from government contractor MITRE, Next Steps Toward Managing Legacy Medical Device Cybersecurity Risks.
LUC Resources and Deliverables
Toolkits/Methodology
AHRMM’s Learning UDI Community (LUC) is a health care collaborative effort, in collaboration with the U.S.