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.

Contact us to discuss your Process Development needs or to request a proposal.