European Union Adopts final Medical Device Regulation: AMDR urges European Member States to “opt in” to CE marking paradigm for SUD reprocessing
Last week marks a milestone for medical device makers, including commercial SUD reprocessors in Europe. After nearly five years of negotiations, the European Union finally passed a comprehensive new EU wide Medical Device Regulation (MDR).
AMDR Position on the European Council’s Partial General Approach to a Proposed Medical Device Regulation
Proposal for a Regulation of the European Parliament and of the Council of the on Medical Devices and Amending Directive 2001/83/EC On behalf of its member companies, the Association of Medical Device Reprocessors (AMDR),
ReMaTec News Turns Spotlight on Reprocessing
ReMaTec News taps into the world of “single-use” device (SUD) reprocessing and in doing so brings news from the FDA-regulated industry of third-party medical device reprocessing to its global readership. The Magazine, which focuses on
Reprocessing: From FDA Regulation to Best Practice
AMDR is honored to be included in the April issue of DOTmed’s HealthCare Business news. AMDR is celebrating its 20th year and the article, written by Dan Vukelich (AMDR’s President and CEO), explores the path
Hospitals Save Millions With Sustainability Programs
Healthcare Finance has come out with a new article that profiles hospitals and how they can save millions of dollars with sustainability programs. Citing advocacy group Practice Greenhealth, the article points out that hospitals are