Product Sterility - Cleanroom testing is required for medical devices, pharmaceuticals, preparations, tissue materials and other materials that claim to be sterile or free of living microorganisms.
This test is performed according to the recommendations in USP General Section 71, ANSI / AAMI / ISO 11737-2, EP 2.6.1, JP and 21 CFR 610.12. All tests are performed in the most advanced ISO Class 5 cleanroom to optimize the aseptic transfer of samples to the test environment. Sterility tests should be validated by performing a Method Compliance (Bacteriostasis / Fungistasis (B / F), Sterility and MPN Method Compliance) test.
Product Sterility - The clean room test evaluates samples for sterility by placing them in growth medium, incubating for at least 14 days, and then checking for evidence of microbial contamination.
Samples can be tested using direct transfer or membrane filtration and using soybean casein digestion broth (soy) or liquid thioglycollate (thio) medium.
USP Method: Samples tested by direct transfer are aseptically immersed in the test medium. Samples tested by membrane filtration (liquids, filterable solids, soluble ointments [oils], and sterile-path devices only) are passed through a 0.45 µm filter, and the filter is immersed in the test medium. A soybean casein broth (soy) medium is used for aerobic and fungal growth at incubation temperatures of 20–25°C. A liquid thioglycolate (thio) medium is used for anaerobic growth at an incubation temperature of 30–35°C. Sample size is determined by both batch size and individual vessel fill volumes.
AAMI Method: Samples tested via direct transfer are aseptically immersed in the test medium. Soybeans are used for aerobic and fungal growth at incubation temperatures of 28–32°C. Sample size depends on lot size, method used, and bioload levels.
After a 14-day incubation, samples are evaluated for the presence of turbidity and / or growth. Media transfer and / or approval test can be done. Error investigation is done when necessary. The recovered organisms are identified and compared with the recovered organisms on monitors performed by the Test Analyst during applicable testing sessions. On the day of the test, it is determined whether there is any abnormality during the sterilization of the sample, during sample processing and / or transportation.
EUROLAB, with its highly expert team and internationally accredited laboratories, Product Sterility Clean Room Test It performs all test, analysis, measurement, evaluation and report generation services completely and reliably.
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