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The transaction aims to enhance operational excellence, unlock additional growth opportunities, and further strengthen Samsung Biologics' position as a leading global multi-modality CDMO.
By: Charlie Sternberg
New capabilities give biologics sponsors more flexibility in upstream process development.
Ready-to-use kit supports faster, more reliable protein production in early-stage biologics research.
Deal expands biologics production support for global biosimilar programs.
The designation supports commercial manufacturing for a potential blockbuster autoimmune therapy.
By: Patrick Lavery
Agreement gives Teva exclusive commercialization rights to proposed ocrelizumab biosimilar in key global markets.
Nona’s BBB technology, combined with Lonza’s biologics and bioconjugation capabilities, aims to enable development for central nervous system therapies.
By: Kristin Brooks
Establishes 20,000-Liter U.S. biologics drug substance manufacturing platform and signs CDMO service agreement.
Industry leaders from Samsung Biologics and Fujifilm Biotechnologies discuss how regional manufacturing, dual sourcing and networked CDMO capacity are reshaping pharma supply chains.
All three facilities are located in Wuxi, China, and combine to provide end-to-end CRDMO services.
New GMP facility strengthens integrated protein therapeutic development and manufacturing capabilities.
J.TRAIN is designed to enable biopharma companies to increase capacity and manufacture biologics at reduced costs and improved productivity.
There is still trial and error, but AI is now demonstrably impacting CDMOs across the entire value chain.
Biosafety testing facility earns fourth EMA GMP certificate with zero critical findings.
The freezing and thawing platform is designed for maximizing process consistency and product quality for high-value biologics.
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