Sterile Processing

In October 2011, more than 275 participants convened at the Food and Drug Administration (FDA) headquarters in Silver Spring, Md., for a multidisciplinary Medical Device Reprocessing Summit sponsored by the FDA in collaboration with the Association for the Advancement of Medical Instrumentation (AAMI). The fall 2011 summit built on an FDA public workshop on reprocessing in summer 2011. For all participants, the summit proved to be an opportunity for a renewed emphasis on performing all the necessary steps in reprocessing reusable medical devices to ensure clean and disinfected or sterilized devicesnot just in the universe of regulations, standards, and best practices, but also in the harried clinical environments and diverse sterile processing centers that are ground zero for reprocessing.