Our sterility testing methods will evaluate your compounded sterile products for the presence of viable bacteria. USP 71 is our roadmap for analysis. Your products are tested within a class 1,000 cleanroom environment. Our methods utilize two different microbiological media, along with two different incubational temperatures to provide a wide spectrum analysis. Incubational periods are 14 days. Preliminary data is available upon request after 72 hours.

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