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Our virotherapy manufacturing services incorporate:

  • Skilled technical transfer capabilities
  • GMP manufacturing of drug substance and drug product
  • State-of-the-art facility including relevant GMP manufacturing licenses (sterile and non-sterile products)
  • Capacity typical for Phase I/II clinical trials with ability to expand as required
  • Highly trained and qualified personnel backed by experienced management team
  • Qualified Person (QP) based on-site
  • Focus on disposable production systems minimizing cross-contamination and operator risks
  • Aseptic processing validation (for non-filterable viruses)
  • Short turnaround times
  • Comprehensive and clear documentation

Why don’t you come and visit us to view our GMP manufacturing facility? We’d love to discuss your project on-site.