Sterilization by Filtration: Validating Filtration for an Aseptic Process
This presentation explores the validation of sterilization by filtration as a critical step in aseptic pharmaceutical processing....
This presentation explores the validation of sterilization by filtration as a critical step in aseptic pharmaceutical processing....
This discussion swims through topics related to disinfection validations of non-critical devices. Including selecting the appropriate level...
As global regulatory pressures tighten and supply chain challenges increase, medical device manufacturers are increasingly considering changes...
Since the installation of the first irradiators for the sterilization of single-use healthcare products in the 1960’s,...
One of the many advancements in the medical device industry has been the advent of reusable robotic...
This webinar examines how rapid sterility testing technologies enhance efficiency, reduce time-to-results, and improve overall product safety...
The presence of 3D printed single-use devices that require processing (cleaning and disinfection or sterilization) at the...
This whitepaper focuses on the importance of disinfectant validations based on real-world conditions to maintain cGMP compliance...
VH2O2 sterilization may leave hydrogen peroxide residuals on the device materials after the sterilization process whose toxicological...
VH2O2 has been a common sterilization option for reusable devices for many years. Interest has increased for...