Medical Device Disinfection for Reprocessing Products for US and EU

Date: 
06/01/2017 (All day)
Duration: 
15-minutes
This webinar is designed for engineers, quality assurance personnel, microbiologists, and marketers of reusable medical device manufacturers to deepen their knowledge about disinfection validation methods for reprocessed devices. Specifically, attendees will better understand disinfection validation standards and practices in the United States and Europe: US FDA Guidance from 2015, AAMI TIR12, AAMI TIR30, ISO15883, among others. Validation techniques and information regarding chemical, thermal, and A0 disinfection testing will be explained.