Sterilization Control

Your autoclave passes the cycle. But is the sterilization actually validated? This article explains what's inside a biological indicator, why one specific organism is used as the global standard for steam sterilization, what your validation file needs to document, and what auditors check for.

Class 1 chemical indicators don't prove sterilization happened. They only confirm the pack went through a cycle. Learn the difference between CI classes 1 through 6, which class your autoclave programme actually needs, and what auditors look for in your sterilization control records. Includes a free CI sample kit offer for food manufacturers and labs in Singapore.

Not all biological indicators work the same way. Learn the 5 BI formats for steam sterilization — and which one your lab actually needs.

Most facilities log temperature, pressure, and cycle time but do you know? It's not a sterilization control programme. The problem Physical parameters confirm the cycle ran but not that sterilization was achieved Dense or improperly loaded chambers can fail to sterilise even when readings look correct Only a biological indicator placed at the hardest-to-reach load point gives direct organism kill evidence Three gaps auditors find No BI programme — organism kill never confirme