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
AMDR White Paper: The Business Case for Reprocessing (2011)
In the United States, where reprocessing has been regulated . . . https://amdr.org/wp-content/uploads/2011/04/Business-Case-for-Reprocessing-for-web-1.pdf
Becker's ASC Review: 10 Important Steps for Sterile Processing in a Surgery Center
By Rachel Fields, Becker's Operating Room Clinical Quality and Infection Control August 25, 2011 Ruth P. Shumaker, RN, BSN, CNOR, a healthcare management consultant who focuses on both ambulatory surgery centers and hospital settings, discusses
Federal Register Notice: Medical Device User Fee Rates for Fiscal Year 2012
DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA-2011-N-0542] Medical Device User Fee Rates for Fiscal Year 2012 AGENCY: Food and Drug Administration, HHS. ACTION: Notice. ----------------------------------------------------------------------- SUMMARY: The Food and
Becker's ASC Review: Single-Use Device Reprocessor Addresses 10 Misconceptions of the Industry
By Leigh Page, Becker's ASC Review August 3, 2011 Lars Thording, PhD, senior director of marketing and public affairs at Stryker Sustainability Solutions, formerly Ascent, responds to 10 misconceptions about third-party reprocessing of single-use devices.