Accelerate Analysis Of Titer, Process Impurities, And Process Contaminants
Accurate titer measurement and impurity analysis are critical to the success of AAV and LV vector process development and manufacturing. Yet traditional methods can be time-consuming and inconsistent. This webinar explores how automated immunoassay platforms are transforming these workflows—offering faster, more reproducible results with less manual effort. Through real-world case studies, the panel will demonstrate how automation can streamline titer and impurity testing across the development and manufacturing continuum, including analysis of host cell proteins, endonucleases, and resin ligand contaminants. Whether you're optimizing upstream processes or scaling for production, you'll gain practical insights into improving efficiency and data quality.
See how automation can elevate your viral vector workflows.
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