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Contract Manufacturing GMP Fill Finish
Integrity Biosolution
Contract Manufacturing

Why Clients Benefit From Our Contract Manufacturing Services

We aspire to become your first choice for contract manufacturing of preclinical and Phase 1 and 2 products. We are committed to superior quality which is embedded into all aspects of our operation. We offer the rapid delivery of product conforming to FDA standards. Our highly qualified and experienced professionals provide a pleasant working environment for our clients.

Integrity Biosolution, an FDA registered company, provides dedicated contract manufacturing services for the aseptic filling of parenteral products entering Phase 1 & 2 clinical studies. Our 2000 sq. ft. clean room suite located in Camarillo, California, was constructed by a national leader, Clean Rooms West, Inc. and validated by Pharmaceutical Services Corporation. Lot sizes range from 100 to 10,000 vials with vial sizes ranging from 2 to 10mL. Lyophilization processing for batch sizes up to 3,000 units is also available. Our GMP testing service facility, automated vial labeling and 100% vial inspection allow us to be your primary source for final drug product manufacturing.

A unique source with Contract Manufacturing Integrated Services:

  • Formulation Development
  • Stability Studies
  • Testing
  • GMP Fill and Finish


 
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