What’s New with Reprocessing Validations for Reusable Medical Devices?
There have been many great strides surrounding the guidance for reprocessing (cleaning, disinfection, and/or sterilization) validations for...
There have been many great strides surrounding the guidance for reprocessing (cleaning, disinfection, and/or sterilization) validations for...
In this podcast from Nelson Labs, business leaders who recently returned from the AAMI standards week meetings...
Standards for reprocessing have become a top priority for regulatory bodies worldwide. The active work around reusable...
The newly revised AAMI ST91:2021 standard provides comprehensive guidelines for the processing of flexible and semi-rigid endoscopes...
Over the past decade, regulatory agencies have increasingly tightened requirements regarding reprocessing validations for reusable medical devices....
Ensuring that reusable medical devices can be properly cleaned, disinfected, and sterilized is crucial for patient safety...
For the past decade, AAMI TIR30 has served as a key guidance document for the cleaning validations...
The cleaning, disinfection, and sterilization of medical devices are critical processes that ensure patient safety and device...
The advancement of reusable medical devices has significantly transformed the medical device industry, bringing about changes in...
Join hosts Jason Pope and Lise Vanderkelen in this informative webinar that will delve into the essential...