Insights On Downstream Manufacturing
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Why Flexible, Tailored CDMO Support Is A Non-Negotiable In Sterile Fill-Finish
4/13/2026
Modern injectable programs require adaptable manufacturing strategies. Learn how flexibility, technical depth, and collaboration reduce complexity, manage change, and protect long‑term supply.
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Optimize Time, Space and Cost With Inline Buffer Formulation And System
4/7/2026
Discover how integrating inline buffer formulation with chromatography reduces buffer waste by 50% and delivers a 710% ROI, transforming downstream efficiency and sustainability.
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Evaluation Of TFF Operating Control Strategies And Scalability
4/2/2026
Gain insight into a comparison of TMP and permeate control strategies for viral vector TFF, highlighting impacts on flux, processing time, impurity removal, and scale-up predictability across development.
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The Effect Of Conventional Cooling Versus Controlled Ice Nucleation On Primary Drying Time
4/1/2026
See how controlled ice nucleation shortens lyophilization cycles, supports higher drying temperatures, and reduces complexity for amorphous and mixed formulations without sacrificing quality.
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Performing Virus Clearance Studies With Retroviral-Like Particles: Updated Guidance
3/26/2026
Updated regulatory standards now support using non-infectious retroviral-like particles for viral clearance. This shift reduces costs and accelerates timelines for biomanufacturers.
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A Gentler Workflow: Fc-fusion Protein Purification With Mixed-Mode And Anion Exchange Chromatography
3/26/2026
Gain insights into comparative performance, workflow flexibility, and practical considerations for implementing a new weak anion exchange hydrophobic resin and a strong anion exchange resin.
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WuXiHigh 2.0 Delivers A 180 mg/mL Formula
3/26/2026
This case study shows how smart formulation and integrated development achieved a stable 180 mg/mL biologic for subcutaneous delivery, for teams tackling concentration issues.
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Tool Enzymes For Antibody-Drug Conjugate Development And Manufacturing
3/26/2026
See how modern tool enzymes enable cleaner, more consistent ADC conjugation, sharper analytics, and a smoother path from research to clinical development — practical guidance for manufacturing.
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Ensure Successful Viral Clearance
3/26/2026
A decade of viral clearance data comparing established and emerging operations, highlighting LRV performance, key process risks, and practical insights to strengthen downstream safety.
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AST Origins: Pioneering RTU Flexibility With Robotic Fill-Finish Systems
3/25/2026
Modernize sterile manufacturing with robotic fill-finish systems. Achieve multi-format flexibility and risk reduction to meet the rigorous demands of personalized medicine and small-batch production.