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CMRP Inventory and Distribution Management Course
This product is also available as a bundle. View BundleJune 08, 2018 | Content Areas: Logistics | Tags: CMRP, Distribution, Inventory Management, MMIS, Shipping and Receiving | Formats: eLearning Course | CPE Credit: 1
Prepare for the revised CMRP examination with the new CMRP eLearning course. This module covers the inventory and distribution management portion of the exam.
May 14, 2018 | Content Areas: Logistics | Tags: Cost Management, Distribution, Inventory Management, Procure to Pay | Formats: Webcast
In this AHRMM webcast, Karen Morlan, administrative director of supply chain operations at Vanderbilt University Medical Center (VUMC), explains the process of PAR optimization to reduce supply chain and nursing staff time, how to maximize the value of a purchase order, and effective strategies to eliminate the need to stock pile. This webcast is also available as an AHRMM podcast.
February 25, 2018 | Content Areas: Logistics | Tags: Data Standards, Regulatory, Suppliers, UDI | Formats: Report/Study
The goal of this document is to provide a guide for supply chain partners to begin a dialogue to ensure that medical devices comply with FDA’s Unique Device Identification (UDI) requirements as well as meet the FDA’s goal of enhancing patient safety. Low Unit of Measure (LUM) programs are complex and the steps outlined in this best practices document are a critical first step. We expect this to be an ongoing process as additional opportunities for stakeholder collaboration continue to arise.
Stewart Layhe, Supply Chain Program Manager at Denver Health, compares the benefits and downsides of perpetual and periodic automatic replenishment (PAR) system inventory methods. This Webcast is also available as an AHRMM Podcast.
September 20, 2017 | Content Areas: Logistics | Tags: Data Standards, Regulatory, Suppliers, UDI | Formats: Report/Study
In this report, Catalog Number Work Group provides the value for inclusion of Catalog Number in Global Unique Device Identification Database (GUDID).
August 31, 2017 | Content Areas: Logistics | Tags: Data Standards, Regulatory, Suppliers, UDI | Formats: Report/Study
A report from the Clinically Relevant Size Work Group, which was convened to examine the utility of device size data in the FDA GUDID system, provide a framework to facilitate correction of existing device size data in the GUDID, and standardize the accurate capture of device size data for new entries into the GUDID.
May 24, 2017 | Content Areas: Logistics | Tags: Data Standards, Regulatory, Suppliers, UDI | Formats: Webcast
In this 3-part webcast series, you will learn about the FDA Unique Device Identification (UDI) “Unit of Use” (UOU). In part one, we will explore the reasons why the FDA created the UOU. We will clarify the differences between the planned use of data standards in healthcare versus their use in other industries. We will explain the difference between UOU and the lowest packaging level, and potential issues in the use of this new identifier. Finally, we will discuss several suggested best practices for UOU. Download talking points and PowerPoint presentation from part one webcast: The FDA Unit of Use (UOU) Explained.