Integrity Bio, Inc performs contract cGMP manufacturing services including aseptic filling of parenteral products for stability, preclinical, and clinical studies.
Our state of the art manufacturing facility located in Camarillo, California is adjacent to our Research and Development Laboratories and houses our Quality Control Laboratories, Stability Laboratory, and Clean Room Manufacturing Suites with Lyophilization processing capability.
Operating within a cGMP environment under centralized Quality Assurance Systems managed by our experienced and dedicated Quality Assurance Department. We aspire to become your first choice for contract manufacturing and are committed to our legacy clients to provide superior quality which is embedded into all aspects of our culture, philosophies, and operations.
We offer the rapid delivery of products conforming to FDA and EU standards. Our highly qualified and experienced professionals provide a pleasant working experience and environment for all of our clients.