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Get practical, data-driven guidance on how to configure internal and external PCDs for ISO 11135–compliant EO sterilization. This white paper explains how to calculate D-values, understand why complete kill occurs at 8 SLR, and align your PCD setup to improve validation accuracy, reduce cycle time, and strengthen sterility assurance.
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Lowering EO use doesn’t have to compromise sterility assurance. This e-book shows how sterilization professionals can reduce EO concentration safely and compliantly by using calibrated PCDs, tighter cycle control, and ISO 11135–aligned validation. Learn how leading teams are cutting emissions, improving consistency, and accelerating release while maintaining patient and operator safety.
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PCDs play a critical role in EO sterilization by offering a standardized, reproducible way to evaluate sterilization performance. Explore how they support process development, validation, and monitoring with reliable, reproducible performance.
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Sterilization validation, like steam, VH₂O₂, and EO, is a critical step in ensuring product safety and regulatory compliance across life sciences and healthcare environments. Read more about best practices to avoid common pitfalls and optimize your validation strategy effectively.
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Biological indicators are widely recognized as the most reliable method for validating sterilization processes in pharmaceutical and medical device manufacturing. Discover why biological indicators are the gold standard for sterilization validation, as well as how choosing the right one ensures safety, compliance, and product integrity.
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