Clinical manufacturing

Our aseptic liquid formulation and filling facility is cGMP validated. We utilize segregated Class 100 aseptic filling suites, controlled manufacturing and processing areas, and on-site QC Chemistry and Microbiology labs.

Key Capabilities Include:

• Vials
• Prefilled syringes
• Lyophilization
• Blow/Fill/Seal
• Recombinant protein manufacturing

Key benefits:

• Proven record of success in tech transfer and scale-up
• FDA & EMEA approved facility
• Seamless alignment with our upstream formulation, analytical and process development capabilities
• Highly flexible suite of capabilities
  • Automated, semi-automated and hand filling
• Significant lyophilization capacity

For capabilities that meet your needs, and outcomes that exceed your expectations, call Catalent today. For more information, please fill out our contact us form or call a member of our sales staff at +1 866.720.3148.