During this 45-minutes webinar, Lise Vanderkelen will take you on a journey to address some of the key aspects of what is required for disinfection validation studies. This is the second step in the processing cycle of reusable devices and the second installment of our three-part webinar series on cleaning, disinfection and sterilization validations of reusable devices.
After watching this session, you should have gained a deeper understanding of:
- Why a validation of the disinfection procedure is crucial to demonstrate the effectiveness of the disinfection.
- The differences between the 3 levels of disinfection.
- The 4 steps that you need to include to have a successful validation (device, contamination, disinfection, evaluation)
- The role of the cytotoxicity test in a disinfection validation.