ABOUT US
With a rich heritage dating back hundreds of years, Cytiva brings a wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery.
We supply the tools and support our customers need to work better, faster, and safer, leading to the delivery of transformative medicines to patients. Our combined portfolio includes well-recognized names such as Allegro™, Supor™, iCELLis™, and Kleenpak™, in addition to ÄKTA™, Amersham™, Biacore™, FlexFactory™, HyClone™, MabSelect™, Sefia™, Whatman™, and Xcellerex™. Visit cytiva.com to learn more.
VIDEOS
WEBINARS
BROCHURES AND DATASHEETS
- Advanced Automation System For Flexible Aseptic Filling
- Closed Robotic Isolator For Reduced Risk And Flexibility In Vial Filling
- Bioreactors Designed For Cell Growth And Expansion
- Antibody Production: Scale-Up Menu
- Allegro MVP Single-Use System
- A Ready-To-Use, Single-Use Liquid Chromatography System
- Mechanistic Chromatography Modeling To Accelerate Process Development
- Selecting An Affinity Chromatography Resin For Your Antibody
- Resin Offering High Productivity And Robust Processes
- Access cGMP Biomanufacturing Capacity Faster
APPLICATION NOTES
- Evaluating Antibody Fragment Purification Using VH3 Resin
- Mild pH Protein A Purification Step With A Mild Elution Resin
- Controlling mAb Aggregates In Chromatography Process Development
- Enhanced Flow Kit Performance With Leak And PUPSIT Testing
- Automated PUPSIT For Drug Product Applications
- Optimized Product Recovery Using The Drug Product Filtration System
- Balancing Protein A Resin Cost, Performance, And Productivity
- Optimizing TFF And SPTFF For High-Concentration mAb Formulations
- Selecting A Platform Filter For High Concentration mAbs
- Production Of A Highly Concentrated Monoclonal Antibody
CONTACT INFORMATION
Cytiva
100 Results Way
Marlborough, MA 08855-1327
UNITED STATES
Phone: 800-526-3593
FEATURED ARTICLES
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mAb aggregation can arise from molecular properties, process conditions, and equipment‑driven stress. Learn where aggregation risk increases across downstream processing and formulation.
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Managing PUPSIT‑related risks is a critical part of contamination control. Learn how bacterial retention studies, wetting fluids, and downstream practices influence sterility assurance.
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When standard water‑based integrity testing falls short, product‑wet approaches can offer a more representative alternative. Learn how risk‑based strategies are used to establish reliable test limits.
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Breakthrough therapies are reshaping medicine, but manufacturing complexity is holding them back. Discover how rethinking production and delivery could expand reach and improve patient experience.
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Explore how real-time kinetic analysis reveals how conjugation, linker chemistry, and drug loading influence antibody–antigen interactions, while enabling sensitive detection of anti-drug antibodies.
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The FDA is rethinking CMC oversight for cell and gene therapies, prioritizing science‑based justification over rigid validation models. Learn how this lifecycle‑focused approach could reduce burden.
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Examine six practical habits that help labs protect equipment performance, prevent avoidable downtime, and strengthen daily workflows, from routine cleaning to IT partnership and scheduled service.
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Strengthen your biomanufacturing reliability with five essential habits focused on preventive care, skilled operators, smart spare‑parts planning, proactive maintenance, and expert support.
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Biopharma innovation is accelerating, but workforce shortages threaten progress. See how strengthening collaboration is essential to developing the skills needed for emerging therapies.
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Breakthroughs thrive when biopharma teams work across silos, yet collaboration remains surprisingly difficult. Explore the barriers and why they persist. What will it take to move beyond them?