Sterilization cycle development
Biological indicator service and support
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Sterilization Cycle Development & Validation

Find the right solution for your product sterilization
Draw on Mesa’s expertise to meet your regulatory requirements and overcome your unique sterilization challenges. Our team works alongside yours to identify the most effective solutions—supporting sterilization cycle development, biological indicators qualification and validation, and routine monitoring. These services help pharmaceutical manufacturers select the most appropriate Biological Indicators to develop and validate robust sterilization cycles.
Expertise
Our experts in product and bioburden resistance analysis help you develop the right sterilization cycles and routine monitoring procedures. We also manufacture custom biological indicators designed to your specifications.
Support
Mesa’s cross-functional service supports your entire process, from bioburden evaluation and product D-value assessment, to sterilization cycle development and routine monitoring.
Compliance
Our laboratory is ISO-certified and FDA-registered for compliance in direct product inoculation and testing all types of products, including controlled substances.