Sterilization is an essential step in the process of producing sterile medical devices. To guarantee sterility, the process of sterilization must be validated. Because there is no direct way to measure sterility, the techniques applied to validate the sterilization process are based on statistical principles. Steam sterilization is the most frequently applied sterilization method worldwide and can be validated either by indicators (chemical or biological) or physical measurements. The steam sterilization conditions are described in the literature. Starting from these conditions, criteria for the validation of steam sterilization are derived and can be described in terms of physical parameters. Physical validation of steam sterilization appe...
Background: Steam sterilisation conditions are not unambiguously quantified in the literature and st...
SYNOPSIS A test piece is described for monitoring the performance of low-temperature steam-with-form...
In practice it is claimed that load characteristics influence a surface steam sterilization process....
Sterilization is an essential step in the process of producing sterile medical devices. To guarantee...
his article provides an update of the validation of moist heat sterilization. It brings together pra...
The purpose of this paper is to provide an overview of the process validation and control validation...
ABSTRACT The process of sterilization in the asepsis pharmaceutical ensures the materials used in th...
Standards require a daily steam penetration test before starting production with a steam sterilizer....
The master’s thesis deals with finding, measurement and evaluation of suitable physical parameters f...
With the growing number of surgical instruments with cavities, e.g. narrow channels, it is important...
The most commonly applied method to sterilize re-usable medical devices in hospitals is steam steril...
Pressure steam sterilization is a commonly used clinical sterilization method, and its sterilization...
The aim of the research was to find an optimal process for a manually operated jacketed steam steril...
A AMI’s newest recommended practice, Compre-hensive guide to steam sterilization and sterilityassura...
Background: Steam sterilisation conditions are not unambiguously quantified in the literature and st...
SYNOPSIS A test piece is described for monitoring the performance of low-temperature steam-with-form...
In practice it is claimed that load characteristics influence a surface steam sterilization process....
Sterilization is an essential step in the process of producing sterile medical devices. To guarantee...
his article provides an update of the validation of moist heat sterilization. It brings together pra...
The purpose of this paper is to provide an overview of the process validation and control validation...
ABSTRACT The process of sterilization in the asepsis pharmaceutical ensures the materials used in th...
Standards require a daily steam penetration test before starting production with a steam sterilizer....
The master’s thesis deals with finding, measurement and evaluation of suitable physical parameters f...
With the growing number of surgical instruments with cavities, e.g. narrow channels, it is important...
The most commonly applied method to sterilize re-usable medical devices in hospitals is steam steril...
Pressure steam sterilization is a commonly used clinical sterilization method, and its sterilization...
The aim of the research was to find an optimal process for a manually operated jacketed steam steril...
A AMI’s newest recommended practice, Compre-hensive guide to steam sterilization and sterilityassura...
Background: Steam sterilisation conditions are not unambiguously quantified in the literature and st...
SYNOPSIS A test piece is described for monitoring the performance of low-temperature steam-with-form...
In practice it is claimed that load characteristics influence a surface steam sterilization process....