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A True One-Stop Target to Market CRDMO

WuXi Biologics uniquely offers a comprehensive single-source array of services from concept to commercialization across the entire monoclonal antibody discovery, development and manufacturing continuum. We can provide integrated technology platforms from target evaluation and identification to final preclinical candidate (PCC) selection (Target to Lead), then onto preclinical development starting from gene synthesis (to initiative cell line development) of the final PCC to IND filing (DNA to IND) as well as cohesive and highly efficient late stage development program through to BLA/MAA submission (IND to BLA). The following list illustrates the primary high-quality services utilized in our integrated mAb technology platform or that could be conducted as an independent standalone service.

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  • Research Material Generation
  • Target Evaluation and Identificatoin
  • MAb Discovery (Antibody Generation & Screening)
    • Hybridoma
    • Phage Display
    • VHH Library
    • Single B Cell Cloning
  • Developability Assessment
  • Lead Optimization
  • In vitro Characterization
  • In vivo Characterization
  • R&D Scale Protein Generation
  • Cell Line Development
  • GMP Cell Banking and Characterization
  • Upstream Cell Culture Development
  • Downstream Purification Development
  • Analytical Development
  • Formulation Development
  • Drug Product Development
  • Pilot Manufacturing
  • Viral Clearance Validation
  • GMP Manufacturing (Drug Substance)
  • GMP Manufacturing / Fill (Drug Product)
  • QC Release and Stability Testing
  • IND Filing / Regulatory Support
  • Technical Transfer
  • Cell Line Development / Optimizatoin
  • GMP Cell Banking and Characterization
  • Upstream Cell Culture Development/Optimization
  • Downstream Purification Development/Optimization
  • Process Characterizatoin and Validation
  • Analytical Development and Validatoin
  • Final Formulation Optimizatoin and Lock
  • Drug Product Development and Process Lock
  • Performance Process Qualification (PPQ) Runs
  • Viral Clearance Validation
  • GMP Manufacturing (Drug Substance)
  • GMP Manufacturing / Fill (Drug Product)
  • QC Release and Stability Testing
  • BLA Submission / Regulatory Support

Our industry experts and highly trained scientific teams have conducted over 450 different integrated mAb client projects throughout early discovery to market launch in our facilities around the globe. We have amassed an unparalleled experience-base amongst CRDMOs thus providing you greater assurance for right-the-first-time project execution.  Let’s get started.

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Let’s discuss your project needs.
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