More Than a CDMO

The End-to-End Support of Your Portfolio

lab safety

Pre-Clinical

Partner with us for cell line and strain development, manufacturability assessments, cell banking and toxicology material generation. Let us guide your path to IND/IMPD submission.

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Clinical Phase I, II

Partner with us to develop your initial clinical process for cGMP drug substance and drug product manufacturing.

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Clinical Phase III

Partner with us to optimize, scale and characterize your process to meet anticipated therapeutic demands.

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Commercialization

Partner with us for process validation and process performance qualification. Leverage our CMC and regulatory services for your BLA/MAA submission and experience our reliability.

Setting New Standards in
Tomorrow’s Medicines

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Billion USD Invested

in recent years

Spotlight

HILLERØD, DENMARK, November 5, 2024 – FUJIFILM Diosynth Biotechnologies, a world-leading contract development and manufacturing organization (CDMO) for biologics, vaccines, advanced therapies, and oncolytic viruses, proudly announces that the first phase of its expansion at the Hillerød site is ready to bring the new production capacity into operation.  
HOLLY SPRINGS, N.C., November 4, 2024, FUJIFILM Diosynth Biotechnologies, a world leading CDMO, today announced that TG Therapeutics, Inc. (NASDAQ: TGTX) has committed to a multi-year manufacturing supply agreement for BRIUMVI® (ublitiximab-xiiy), its U.S. FDA-approved therapeutic for relapsing forms of multiple sclerosis (RMS). 
August 20, 2024 – FUJIFILM Diosynth Biotechnologies, a world leading contract development and manufacturing organization (CDMO) for biologics, vaccines, advanced therapies, and oncolytic viruses, today hosted a celebration for the opening of its microbial fermentation manufacturing facility in Billingham.

In the News

Business Update

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April 16, 2024 – FUJIFILM Diosynth Biotechnologies today announced the decision to globally restructure its Small Scale Business Unit, that may…