Literature / Brochures
Mammalian Cell Culture Manufacturing
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New State-of-the-art Manufacturing Facility ready for GMP production
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All Single-Use technology – fully disposable upstream and downstream
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Facility designed to accommodate further expansion and equipment needs
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More Literature / Brochures by Chiron Recombinant Proteins
More Content From Chiron Recombinant Proteins
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It is important to ensure process elements like scalability, sourcing raw materials, and GMP adherence are considered during process development.
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A CDMO helps organizations predict and mediate technical transfer risks for a successful project start.
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In these exceptional circumstances, what we do matters more than ever.
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Process development is a crucial stage in biopharmaceutical manufacturing.
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Successful and rapid analytical method development plays a key role in ensuring the development of robust processes to produce high-quality products.
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The new facility, equipment, and automation systems ensure reliable production of antigens for blood supply safety and patient health.