Knowledge Center

This page provides information about submitting data to the database for device Labelers, entities responsible for providing the data to the GUDID.

How-to guide to managing IV disruptions. Download Tool

The Food and Drug Administration (FDA) UDI system is being phased in over several years. The first sunrise date (certain Class III devices) occurred 09/24/14. Recognizing UDI implementation will take time, healthcare supply chain and risk management professionals should be aware of already-implemented changes in the FDA’s adverse event reporting methodology. One of the changes required immediately is the use of the UDI in adverse event reporting.

AHRMM Education and Professional DevelopmentI want to obtain or renew the Certified Materials & Resource Professional (CMRP) credential. Refer to AHRMM's CMRP Certification page for more information and helpful resources on CMRP.

Have questions on education, certification, conference, the CQO Movement and more? Check out some of AHRMM's frequently asked questions to help you…

  Price: Member: FREE  |  Non-Member: $99.00 CEC Hours: 1

The page provides information about the AHRMM Board, Committee and Fellow Frequently Asked Questions.

Join us at AHRMM24 Conference & Exhibition, September 22-25 in Columbus, Ohio for the leading event for health care supply chain.

Continuing Professional Education (CPE) Contact Hours are offered through various educational events and eLearning courses for CMRP certification

AHRMM Career Center offers a variety of resources, including career counseling, job search assistance, resume and cover letter review, and networking opportunities.

AHRMM Publications such as Supply Chain Strategies & Solutions, provide up-to-date information on the latest health care supply chain news.