Sterile Processing

In 2011, there were two events at the Food and Drug Administration (FDA) headquarters where the key issues of medical device reprocessing were raised and discussed. The first event was put on by FDA staff, with an assist from the Association for the Advancement of Medical Instrumentation (AAMI). During this two-day meeting in June, a parade of industry experts presented their research and experience to describe the key challenges facing the healthcare industry when it comes to effective device reprocessing.