About sterilization validation

Our company also conducts sterilization validation services, various bacterial tests, and residual gas analysis.

At Steritech Co., Ltd., we conduct sterilization validation services. We perform pre-conditioning to adjust temperature and humidity to ensure that products are in a state that is easy to sterilize, and we also remove air from the products by applying vacuum and introducing EOG, among various other processes. Please feel free to contact us when you need our services. 【Examples of Sterilization Processes】 ■ Pre-conditioning ■ Vacuum ■ Humidification ■ EOG Introduction ■ Action Time ■ Air Replacement *For more details, please refer to the PDF materials or feel free to contact us.

basic information

【Business Details】 ■Partial Cycle: Confirm that the resistance of product-attached bacteria is less than the internal PCD resistance. ■Cycle Development - Confirm changes in the lethality rate of internal PCD by altering sterilization conditions (temperature, pressure, EOG exposure time). - Confirm that the resistance of internal PCD is less than that of external PCD. ■Half Cycle: Confirm the EOG exposure time at which the lethality rate of internal PCD is 100% and some external PCD survive. ■Full Cycle: Confirm that there are no issues with the product even under excessive temperature, humidity, pressure, and exposure time. ■Daily Sterilization Conditions: - The sterilization action time is set to double the time determined in the half cycle, with the temperature, humidity, and action pressure of the half cycle as the lower limits. - The temperature, humidity, and action pressure of the full cycle serve as the upper limits. *For more details, please refer to the PDF document or feel free to contact us.