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Providing expert, world-class CRDMO services for mRNA and related products

WuXi Biologics provides extensive top-tier CMC development capabilities and GMP manufacturing capacity tailored for mRNA therapeutics and vaccines. From initial plasmid DNA manufacturing to GMP production of drug product (DP), our expert team offers high quality end-to-end services. Our GMP facilities include a microbial-based manufacturing unit for plasmid DNA production, alongside multiple vessels for mRNA transcription. Furthermore, we provide state-of-the-art mRNA-LNP production systems, robust downstream / purification platforms and robotic aseptic filling systems for DP manufacturing. Grounded in our exceptional in-house CMC development and manufacturing expertise, executional excellence, and world-class quality system, our mRNA service platform ensures unparalleled support for your projects.

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  • Research Materials Generation
  • Plasmid DNA engineering and cloning
  • Plasmid Process Development and Production
  • RNA / mRNA in vitro Transcription Process Development
  • Purification Process Development
  • Analytical Development
  • Formulation Development
  • Drug Product Development
  • Pilot Manufacturing
  • GMP Manufacturing (Drug Substance)
  • GMP Manufacturing / Fill (Drug Product)
  • QC Release and Stability Testing
  • IND Filing / Regulatory Support
  • Technical Transfer
  • RNA / mRNA in vitro Transcription Process Development / Optimization
  • Purification Process Optimization / Characterization
  • Process Characterizatoin and Validation
  • Analytical Development and Validation
  • Final Formulation Optimization and Lock
  • Drug Product Development and Process Lock
  • Performance Process Qualification (PPQ) Runs
  • GMP Manufacturing (Drug Substance)
  • GMP Manufacturing / Fill (Drug Product)
  • QC Release and Stability Testing
  • BLA Submission / Regulatory Support

We have established highly-efficient processes and technology platforms to expedite your path to IND filing and beyond. In addition, our established global quality system, quality control and operational systems meet or exceed worldwide regulatory standards from the U.S. FDA, EMA, NMPA and other major regulatory agencies. Our commitment to quality is ingrained in our company culture and our employees. Let us help you bring your next biologic into clinic tials for the benefit of patients worldwide.

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Let’s discuss your project needs.
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