Reprocessing Validations Flexible Endoscopes and AAMI ST91
The newly revised AAMI ST91:2021 standard provides comprehensive guidelines for the processing of flexible and semi-rigid endoscopes...
The newly revised AAMI ST91:2021 standard provides comprehensive guidelines for the processing of flexible and semi-rigid endoscopes...
Virucidal efficacy testing is essential for determining the effectiveness of disinfectants or antiseptic products against viruses. This...
In 2018, TC194, the ISO committee responsible for biocompatibility, released a new version of the 10993-1 standard....
In this insightful webinar, originally presented at Pharmapack Europe 2022, S. Ross Tsakas, Pharmaceutical Segment Leader at...
Ethylene Oxide (EO) sterilization technology is crucial for enabling critical medical products and devices to safely reach...
The release of ISO 10993-1 in 2018 marked a significant shift in the biocompatibility evaluation of medical...
All hand sanitizers, whether used by consumers or healthcare professionals, are considered over-the-counter (OTC) drugs regulated by...
When developing a disinfectant or sanitizer (herein referred to as disinfectant) for use on environmental surfaces, the...
Ethylene Oxide (EO) sterilization is one of the most complex sterilization methods commonly used, with numerous approaches...
Over the past decade, regulatory agencies have increasingly tightened requirements regarding reprocessing validations for reusable medical devices....