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Discover how rapid microbiological methods can reduce your turnaround time in cell therapy manufacturing while remaining compliant with evolving regulatory expectations. This webinar will provide actionable insights on the importance of contamination control strategies and how to implement rapid QC methods that address the unique needs of cell therapy. It will further highlight the challenges that manufacturers face in microbial QC.
The speaker will discuss approaches for strengthening contamination control and tailoring QC approaches to improve product release timelines. Supporting data on rapid sterility testing will demonstrate how optimizing incubation conditions and supplementing culture media can significantly enhance detection timelines.
By the end of this session, attendees will be able to evaluate the potential of rapid methods for their own workflows, align their QC strategies with regulatory trends, and consider solutions that accelerate operational efficiency to contribute to better patient & market access.
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