The quality of our biologics and pharmaceuticals is just as important as their development. KindredBio will manufacture products under the appropriate regulatory frameworks such as Title 9 and Title 21 of the Code of Federal Regulations for products being licensed through the USDA and FDA respectively. KindredBio manufacturing sites in Burlingame, CA and Elwood, KS follow Current Good Manufacturing Practices (cGMP).
KindredBio acquired, retrofitted, and commissioned an additional manufacturing facility in Elwood, Kansas. We are uniquely positioned to meet the manufacturing needs of our promising pipeline with combined facilities reaching 180,000 square feet of full-spectrum production, from infancy to commercialization, including labeling and packaging end-to-end processes. KindredBio Clinical and Commercial Manufacturing can support the production of a broad range of biologics and pharmaceuticals. This is done through the use of single-use bioreactor (SUB) up to 2,000L in size and the use of automated vial filling, labeling, and cartoning equipment providing flexibility throughout the process.
In addition to the Kansas facility, KindredBio commissioned its own dedicated cGMP biologics manufacturing facility in close proximity to our development labs in Burlingame, California. The facility utilizes state-of-the-art single-use technology and has the capacity to meet the requirements for the small scale clinical and commercial KindredBio biologics supply.
KindredBio is one of the few biopharmaceutical manufacturers that can capitalize on its production capacity and maintain a steady revenue stream while ensuring all fulfillment needs are met.
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