We are a world leader in cGMP* Contract Development and Manufacturing supporting our partners in the development and production of their biologics, vaccines and gene therapies.

Our commitment is to help deliver our customers’ therapies to their patients, whether they are in clinical development or are commercially approved. We do this through the application of good science, our knowledge of the clinical process and our quality driven approach. With over twenty five years of experience we have become a trusted partner to a wide range of pharmaceutical companies in the industry.

Road to clinical success

Our development philosophy is driven by designing processes that have phase appropriate product controls. Quality is at the heart of everything we do, driving the development and the successful production of our partner’s therapies from beginning to end.

Working with an experienced contract development and manufacturing partner is the key to bringing new products to market with increased efficiency and speed. We offer our customers highly flexible clinical and commercial cGMP facilities for the production of recombinant proteins, vaccines, onoclonal antibodies, among other large molecules, viral products and medical countermeasures expressed in a wide array of microbial, mammalian, and host/virus systems.

With you every step of the way

As your partner, we help expedite this process by bringing our years of experience, range of capabilities across our network, and our expression platform technologies for microbial expression, by bringing our years of experience and range of capabilities across our network. We offer services from cell line development using our proprietary pAVEway™ microbial and Apollo™ X cell line systems to process development, analytical development, clinical and FDA-approved commercial manufacturing.

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FUJIFILM Diosynth Biotechnologies, U.S.A., Inc.

*Current Good Manufacturing Process