Medical device reprocessing, and the scientific validation of reprocessing instructions, are critical
steps to ensuring devices are safe and effective for patient use. The pandemic caused by severe
acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus responsible for COVID-19,
as well as past infection outbreaks, have prompted increased concern over disinfection and
sterilization of reusable medical devices.
Whitepaper
WHITEPAPER
Disinfection Validation: How to Classify and Validate Your Medical Device Disinfection Process
January 20, 2021 | By: Alpa Patel, Wendy Mach and Jeralyn Franson
Complete the following information to access the whitepaper