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: