AMDR Submits Comments to FDA’s Reprocessing of Reusable Medical Devices Docket
On September 26, 2011, AMDR submitted comments to FDA’s docket seeking input on the reprocessing of reusable medical devices: In AMDR’s August 1, 2011 comments, we highlighted that FDA’s experience in regulating the reprocessors of SUDs applies to its
ProtectOurSavings.com Blog: Know Your Rights
Originally Posted September 21, 2011 by AMDR President, Dan Vukelich Hospital purchasing personnel are familiar with a variety of tactics that some original equipment manufacturers (OEMs) employ in an effort to maximize sales of their
Press Release: Reprocessing Industry Overwhelmingly Supported by U.S. News & World Report’s 2011-12 Honor Roll Hospitals
Washington, DC - Every year, U.S. News & World Report releases their annual list of the Best hospitals across the country, by specialty, including the highly coveted “Honor Roll” list that distinguishes the best of
AMDR Co-Sponsors Alliance for a Stronger FDA Ad in Capitol Hill Papers
Along with numerous other organizations in the health and food sectors, AMDR is proud to have co-signed the Alliance for a Stronger FDA's advertisement which ran in several Capitol Hill papers September 6, 2011. Noting that the
AMDR President to Present at 2nd Healthcare Development Conference
AMDR President Daniel J. Vukelich will present at the 2nd Healthcare Development Conference in Chicago October 26. Presenting, "Reprocessed Medical Devices: A Sustainable Solution," at 4 PM on Wednesday the 26th, Vukelich will highlight
Meeting Announcement: 2011 AAMI/FDA Medical Device Reprocessing Summit
Mark Your Calendar! Don’t miss this timely event to address challenges recently highlighted by the U.S. Food and Drug Administration (FDA) on the reprocessing of reusable medical devices. Building from the FDA’s public meeting