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

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…
Investment to create an additional 680 highly-skilled local jobs by 2031; Adding large-scale production capacity to robust global network through state-of-the-art manufacturing hubs in the United States and Europe
HILLERØD, Denmark, March 25, 2024 – FUJIFILM Diosynth Biotechnologies, a world-leading contract development and manufacturing organization for biologics, vaccines, advanced…