Our Biological Indicators (BI) service provides critical tools and expertise for validating sterilization processes and ensuring microbial lethality. BIs are standardized preparations of resistant microorganisms used to challenge sterilization cycles—offering direct evidence of process efficacy and compliance with global standards such as ISO, USP, FDA, and EU GMP. Our team can help you with all your biological indicator needs, whether its selection, qualification, usage interpretation or troubleshooting unexpected results.
Our Chemical Indicators (CI) service provides essential tools and expertise for monitoring sterilization processes. Chemical indicators offer visual confirmation that sterilization parameters—such as temperature, time, and exposure to sterilant—have been met. They are a critical component of routine monitoring, load release decisions, and equipment qualification across various sterilization methods. Our team can help you with selection, qualification, usage interpretation or troubleshooting unexpected results.
Our Sterilizer Cycle Validation Support service ensures that sterilization processes consistently achieve the required microbial lethality and product safety standards. We provide expert guidance and technical support for the validation of steam, dry heat, ethylene oxide (EtO), and hydrogen peroxide vapor sterilization cycles—helping organizations meet regulatory expectations and maintain aseptic integrity.
Our Sterilizer Cycle Failure Investigation service provides rapid, expert analysis of sterilization process deviations to identify root causes, assess risk, and restore validated conditions. Whether the failure involves steam, dry heat, EtO, or hydrogen peroxide vapor sterilization, we help organizations respond decisively to protect product integrity, patient safety, and regulatory compliance.
Our VHP Decontamination Support service provides expert guidance for the safe, effective use of vaporized hydrogen peroxide in critical environments. Whether you're preparing for cleanroom qualification, responding to contamination events, or maintaining aseptic conditions, we help ensure your VHP cycles meet microbial reduction targets and regulatory standards.
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