Protein Formulation and Process Development along with GMP Fill Finish Services from a Single Experienced Source

Contract Manufacturing Services

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 is located in Camarillo, California in close proximity to our Research and Development Laboratories and houses our Quality Control Laboratories, Stability Laboratory, and Clean Room Manufacturing Suites with Lyophilization manufacturing 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 fill a variety of formats including vials, syringes (prefilled), cartridges, bottles, and our container closure system Lyotip.

We offer the rapid delivery of products conforming to California FDA, US FDA, and EU standards. Our highly qualified and experienced professionals provide a pleasant working experience and environment for all of our clients.