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Biologics process development is an active undertaking that seeks continuous improvement along the entire length of the drug development timeline.
Released By Scorpius BioManufacturing
Clinical manufacturing of cGMP-compliant mammalian cell culture processes is a complex and resource-intensive effort that presents several challenges.
The biologics CDMO selected for a given product or program is critical to an innovator’s ability to deliver a drug product safely, on time, and on budget.
The value biologics CDMOs provide their innovator customers has changed radically in recent years, presenting new questions that must be answered.
While crafting a RFP to capture the information innovators need to select a CDMO partner has always been critical; it has grown increasingly complicated.
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