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Optimizing Supply Chain using UHF-RFID Technology

Webcast
Lana Makhanik and Peter Fiorentino discuss discus why Beth Israel Deaconess Medical Center is breathing easier after they overhauled their inventory management system using Ultra high frequency (UH

Optimizing Supply Chain using UHF-RFID Technology

Webcast
This video reviews the benefits of RFID implementation, and the successes and lessons learned from a local medical center.

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).

UDI Forum 2024 | October 29-31

Get critical feedback and guidance from experts who have successfully implemented the UDI and discover the direct benefits the UDI can provide to your supply chain, to your workflows, and to the safety of your patients.

FDA advises against using plastic syringes made in China

U.S. health care organizations should immediately transition away from using certain unauthorized plastic syringes made in China by Jiangsu Caina Medical Co. and Jiangsu Shenli Medical Production Co., and should only use other plastic syringes made in China until they can transition to alternatives, the Food and Drug Administration announced.

FDA approves combo test for flu, COVID-19; alerts providers to medical device risks 

The Food and Drug Administration recently granted emergency use authorization for the first over-the-counter home antigen test to detect both flu and COVID-19.

Medical Products of Human Origin, UDI and ICCBBA: Supply Chain’s Role

Webcast
Supply chain is in the unique position, working with so many different disciplines within the hospital, that it is natural that they initiate conversations on the proper management of these product

Medical Products of Human Origin, UDI and ICCBBA: Supply Chain’s Role

Podcasts
AHRMM Podcast on how supply chain should be interdepartmentally conversing to determine the handling of human-origin medical products and their UDIs.

AHRMM Awareness Brief: Draft Guidance for UDI Convenience Kits

Issue Brief
This Awareness Brief provides a quick reference to the Draft G

AHRMM Comment Letter to FDA Regarding the Draft Guidance for Industry on the Global Unique Device Identification Database (GUDID)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