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Adopting current best practices is critical to helping mitigate risks like production delays and compliance penalties in manufacturing. Learn about effective strategies that can streamline your analytical method transfer process.
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Traditional compendial safety and impurity tests can take days or weeks to process. Learn how rapid molecular methods like qPCR for mycoplasma, sterility, and lentiviral quantification are key to accelerating product release and timely treatment delivery.
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Rapid qPCR testing provides a sensitive, accurate, and streamlined alternative to 28-day culture methods for mycoplasma and sterility testing in cell therapy manufacturing. This rapid turnaround supports greater workflow efficiency and improved risk mitigation.
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Achieving regulatory compliance for biotherapeutics requires streamlined analysis. Learn how automated, integrated software can simplify complex data from residual DNA and contaminant assays, providing actionable results while ensuring data traceability and compliance.
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