INSIGHTS ON POLISH & VIRAL FILTRATION
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Virus Retention Performance Under Diverse Processing Conditions
Virus filtration is robust across a wide range of process parameters, including high protein concentration and flow decay. Discover how retention relies on size exclusion to simplify risk assessment.
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Cell Culture Media Mixing In A Benchtop Single-Use Mixer
Explore how efficient powder-liquid mixing and sterile filtration preserve media integrity and support reproducibility in biopharmaceutical workflows, with promising scalability for larger-volume applications.
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Quality Control In IVT RNA Workflow
Accurate sizing and purity checks are essential in IVT RNA workflows. Explore how automated electrophoresis improves QC efficiency and ensures RNA integrity for downstream applications.
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An Innovative Solution For Continuous Low pH Flow-Through Virus Inactivation
Continuous biomanufacturing is reshaping how active pharmaceutical ingredients are produced. Learn how modular, automated virus inactivation solutions are helping manufacturers improve efficiency.
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An Efficient End-To-End AAV8 Platform Process
Explore a scalable AAV production platform that improves full capsid yield and dramatically reduces host cell impurities, offering a practical solution to common manufacturing challenges.
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Tools For Efficient And Reliable Gene Therapy Manufacturing
Discover scalable strategies for overcoming AAV purification challenges, from low yield and impurity removal to serotype variability, as well as how advanced tools can streamline manufacturing.
POLISH & VIRAL FILTRATION WEBINARS
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Biopharma Supply, Reimagined: Blarney, A Climate-Neutral Facility For Best-In-Class Filters
Explore how a new, climate-neutral manufacturing facility strengthens biopharma supply chains. Understand the benefits of its advanced filtration technologies and commitment to environmental sustainability.
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Sterile Filtration: Filter Sizing For Process Optimization11/11/2025
Correctly sizing sterilizing-grade filters is crucial for optimizing sterile filtration processes. Learn how Pmax and Vmax methodologies impact efficiency, cost, and filter performance, including the role of pre-filters.
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Scale Up: Supporting Easy Scalability All The Way To Manufacturing11/11/2025
Achieve seamless purification scale-up from development to manufacturing using integrated chromatography and TFF systems. Optimize workflows, ensure batch consistency, and accelerate time to market.
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Optimize DNA Clearance In High-Salt, GMP-Grade Purification Processes10/28/2025
Explore how salt-active endonucleases overcome DNA clearance challenges in viral vector purification by digesting down to 3–5 nucleotides and performing reliably in high-salt conditions.
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Overcoming Downstream Challenges In Next-Generation Antibody Development10/8/2025
Unlock expert strategies for navigating the complex downstream purification and process challenges inherent in developing next-generation antibodies. Design for scalability from the start.