Search results for "Cytiva" in Articles / App Notes
Article
Basics in Process Development for Biotherapeutics
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Definitions, activities, and things to consider when developing an upstream or downstream bioprocess.
Article
High-Quality Chromatography System Meets Predesigned DeltaV for Integrated Manufacturing
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Nearly 50% of the warning letters issued by the FDA cite 21 CFR data integrity violations. Implementing a distributed control system for facility-wide control of …
Article
Manage HCPs and Enhance Your Route to Market
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Host cell protein (HCP) management is critical to biologics development—and getting it wrong could delay your development cycle. Learn how the right HCP strategy can enhance…
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Getting Your Investigational Drug Regulatory Ready
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Navigating regulatory requirements can be overwhelming. This article outlines basic strategies for efficient regulatory review and drug approval.
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HyClone Characterized FBS – Origin Equivalence Study
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Fetal bovine serum (FBS) is still used in many cell culture applications, including viral vector production. FBS from a single origin may be limited, so qualifying FBS from …
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Process Development Quiz: How Well Do You Know Your Essentials?
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Planning for IND
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Learn how to navigate regulatory requirements as you progress through clinical trials to commercialization.
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Making Your Bioprocesses More Efficient
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Bioprocess intensification lets you maximize productivity while minimizing one or more key variables of your current biomanufacturing proces…
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Recent Development in Fibro Technology
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Fibro technology enables rapid cycling chromatography to accelerate research and process development, as well as increased productivity in large-scale manufacturing. T…
Article
Purifying Tagged Proteins: Learn the Basics
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What is tagged protein purification? When and why should you use it? Learn the basics in our quick guide to tagged protein purification.