To develop effective and well tolerated therapies, KindredBio ensures the quality of our products. The FDA regulates the manufacturing of both human and veterinary pharmaceuticals. KindredBio develops and manufacturers our products in compliance with Current Good Manufacturing (cGMP) requirements, including at our biologics manufacturing facility in Burlingame, CA and our planned second facility in Elwood, KS. When we require outside manufacturing, KindredBio ensures the external Contract Manufacturing Organizations (CMOs) follow cGMP standards.
At KindredBio, development and manufacturing teams work together seamlessly. Our facilities meticulously transfer the molecules from the development to the manufacturing stage. The teams ensure that all steps and processes are performed in line with our quality standards, allowing us to produce dependable, species-specific veterinary biologics and pharmaceuticals.