In cell therapy production, rapid sterility testing plays a critical role in helping to ensure the quality and safety of the final product. Given the fast-paced nature of this production process and the limited shelf life of cell therapy products, it is imperative to detect and prevent any further contamination as early as possible in the workflow, such as testing raw materials or in-processing samples. By implementing rapid sterility testing, potential sources of contamination can be uncovered and addressed promptly, helping to reduce the risk of product loss and unexpected production delays and outcomes. This not only enhances the overall efficiency of the workflow, but also helps to maintain the integrity and efficacy of the cell therapy product.
The Applied Biosystems SteriSEQ Rapid Sterility testing system is an integrated, real-time PCR (qPCR) solution for rapid sterility testing of cell therapy products. The SteriSEQ Rapid Sterility Testing workflow provides a simple, easy-to-implement approach to contaminant detection, with a functionally confirmed, commercially available qPCR assay kit and industry-leading, real-time PCR instruments with dedicated analytical software to help enable regulatory compliance.
Key system features:
Central to the SteriSEQ Rapid Sterility Testing System is its robust, multiplexing qPCR assay. Leveraging the high performance of trusted TaqMan chemistry, the SteriSEQ Assay can detect more than 16,000 bacterial species plus 2,600 species of fungi* and can detect contamination in raw materials and in-processing samples in cell densities up to 1e6 cells.
Key assay features:
*Based on in-silico testing
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