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One-stop CDMO services for VLP products

WuXi Biologics offers dedicated VLP R&D labs and microbial fermentation GMP production facilities for the development of VLP products. Our services span from initial virus construction through to IND filing and beyond. Explore our extensive array of integrated CMC development services and clinical manufacturing capacities for VLP production, scalable up to 300 L.

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  • VLP Engineering and Construction
  • Strain Development, Banking and Characterization
  • VLP Bank Generation (GMP) and Characterization
  • Reference Standard Generation and Characterization
  • Fermentation Process Development / VLP Harvest
  • Purification Process Development
  • Analytical Development
  • Drug Product Development
  • Pilot Manufacturing
  • GMP Manufacturing (Bulk Substance)
  • GMP Manufacturing / Fill (Final Product)
  • QC Release and Stability Testing
  • IND Filing / Regulatory Support
  • Technical Transfer
  • Strain Development / Optimization
  • GMP Cell Banking and Characterization
  • Fermentation Process Optimization / Characterization
  • VLP Harvest Development / Optimization
  • Purification Process Optimization / Characterization
  • Process Characterizatoin and Validation
  • Analytical Development and Validation
  • Drug Product Development and Process Lock
  • Performance Process Qualification (PPQ) Runs
  • GMP Manufacturing (Bulk Substance)
  • GMP Manufacturing / Fill (Final Product)
  • QC Release and Stability Testing
  • BLA Submission / Regulatory Support

Collaborating closely with you, our industry experts and skilled scientific teams craft an optimal and efficient project plan for your product and process needs. Leveraging our high-quality systems, robust development platforms, and advanced technology, we ensure precise project execution from the outset.

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Let’s discuss your project needs.
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