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Viral Vector Process Development: From Gene To Product
Process development plays a critical role in viral vector manufacturing as it establishes and optimizes suitable cell culture and purification methods, and develops analytical assays for product quality confirmation. A robust process can yield higher potency, increased productivity, reduced impurity profile, and lower costs. Choosing the right contract development and manufacturing organization (CDMO) partner with a skilled team is crucial for successful product development in the rapidly evolving field. Matica Bio offers comprehensive support from development to GMP production, accelerating drug development with high-quality services that include cell line development, platform adaptation, media optimization, culture characterization, closed system transition, scaling, cryopreservation, and dose delivery mechanism development.