Insights On Polish & Viral Filtration

  1. Virus Retention Performance Under Diverse Processing Conditions 11/14/2025

    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.

  2. Cell Culture Media Mixing In A Benchtop Single-Use Mixer 11/13/2025

    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.

  3. Quality Control In IVT RNA Workflow 11/12/2025

    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.

  4. An Innovative Solution For Continuous Low pH Flow-Through Virus Inactivation 11/5/2025

    Continuous biomanufacturing is reshaping how active pharmaceutical ingredients are produced. Learn how modular, automated virus inactivation solutions are helping manufacturers improve efficiency.

  5. An Efficient End-To-End AAV8 Platform Process 11/5/2025

    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.

  6. Tools For Efficient And Reliable Gene Therapy Manufacturing 11/5/2025

    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.

  7. Overcoming Scale-Up Challenges In Viral Vector TFF 10/29/2025

    Discover how a tailored TFF solution delivers a scalable, high-yield process that integrates smoothly with existing infrastructure and maintains regulatory compliance.

  8. Achieve Higher Targeted Concentrations 9/30/2025

    Single-pass TFF streamlines downstream processing by reducing footprint, shear exposure, and hold-up volumes. Learn how this approach is advancing efficiency across therapeutic and vaccine production.

  9. Performance Of The DIANT sp2TFF System Across Different Flow Regimes 9/18/2025

    A dual-stage TFF system has been proven to reliably perform buffer exchange and concentration under both high- and low-flow conditions, demonstrating its versatility and low-pressure stability.

  10. Measure And Control In-Line Protein Concentration 8/5/2025

    Streamline protein and antibody purification with an automated TFF system featuring real-time, in-line concentration measurement for enhanced accuracy, reliability, and cGMP compliance.