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
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.