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Navigating the Economic Storm: A Prescriptive Approach for Healthcare Supply Chain Professionals

Magazine & Journal Articles
In this page, AHRMM recommends these 3 proactive activities in the event of economic downturn.

AHRMM Statement on Comparative Effectiveness

Letter/Comment
AHRMM supports the concept and use of Comparative Effectiveness Research (CER) to provide evidence-based data to help inform purchasing decisions.
Public

AHA Letter on EPA's Proposed Standards for the Use of Ethylene Oxide

AHA comments on the Environmental Protection Agency’s (EPA) proposed standards for the use of ethylene oxide (EtO) to sterilize medical devices.

Ethylene Oxide Device Sterilization and the Alternatives

On-Demand Educational Webinars
In light of the closure of some facilities that use gas ethylene oxide (EtO) to sterilize medical devices prior to their distribution and use, the FDA is looking at the future availability of medical devices and the possibility of medical device shortages. This webinar highlights potential alternatives to EtO, their advantages and disadvantages, and how to determine what kind of sterilization is best for your organization.

Reprocessing Single Use Devices (SUD) RFP

Request for Proposals (RFP)
Please see a sample of a Reprocessing Single Use Devices (SUD), RFP below - you will find this short document and the Reprocessing Narrative Evaulation example covers all the basics, and you

Improving & Managing the Sterilization Process Through the Use of Surgical Instrument Management Software & Lean

White Papers
The surgical instrument management software (SIM) implementation began in October of 2003 and a Lean initiative to redesign processes began in October 2005.

Developing a Socially Responsible Closed Loop Supply Chain

White Papers
The initial purpose for developing a socially responsible, closed loop supply chain was to enhance our environmentally sustainable practices by purchasing more responsible and locally sourced pro

Ethylene Oxide Device Sterilization and the Alternatives

In light of closures and potential closures of certain facilities that use gas ethylene oxide (EtO) to sterilize medical devices prior to their distribution and use, the FDA is concerned about the