Process Development for cGMP Manufacturing Company, Cytovance Biologics
 
 

Process Development

Cytovance® Biologics can develop processes de novo or can transfer-in existing processes to be optimized or scaled-up to meet regulatory or economic requirements. We take time to ensure that we fully understand every client's short- and long-term technical and business needs and develop processes accordingly. We strive to deliver processes that are:

    • Cost effective
    • Robust
    • Scaleable
    • Validatable
    • Compliant
    • Transferable

Cytovance provides a full complement of process development and analytical development services critical to a complete and successful manufacturing project, including:

    • Cell Culture Development with bench scale non-cGMP production
    • Recovery and Purification Development
    • Analytical Development and Validation
    • Cell Line Development
    • Final Product Fill/Finish Development
    • Process Troubleshooting
    • Technology Transfer

Our process development labs and equipment are state-of-the-art and our staff has worked as a team for several years. We have special expertise in recombinant proteins with complex glycosylation requirements, a critical component of many therapeutic products. Cytovance's team has experience in the development and production of numerous products now introduced into the worldwide market.