ANSI/AAMI provides guidance on quality assurance monitoring in medical device reprocessing. Our workshop will take a deep dive into what the standards describes as a quality management system (QMS) and how to get started in your department. Covering topics from equipment testing to cleaning verification, this discussion will review various elements of quality management, who is responsible and how to get started or improve what’s already in place.

Using interactive resources, you’ll identify proactive and reactive quality measures and their role in medical device reprocessing.

By the end you’ll take home an outline containing requirement references, a space for stakeholders and working group recommendations and other next steps to design a compliant and comprehensive quality management system.