Insights On Downstream Manufacturing

  1. 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.

  2. ADC Purification Without Compromise 9/16/2025

    Explore how advanced filtration technology is helping streamline ADC manufacturing, reduce operator risk, and improve batch consistency through automation, remote operation, and real-time DAR monitoring.

  3. Delivering Excellence In Every Sterile Injectable 9/4/2025

    Learn how partnering with a trusted CMO to navigate the complexities of sterile injectable manufacturing can ensure your life-changing therapies reach patients safely, efficiently, and at the highest quality.

  4. Navigating The Complexities Of Pre-Filled Syringe Manufacturing 9/4/2025

    Drawing on our extensive expertise in sterile injectables (SI), here, we highlight practical strategies and proven solutions designed to help navigate challenges and support the reliable, scalable production of high-quality PFS therapies for patients worldwide.

  5. Modular Systems Explained 9/3/2025

    Modular bioprocessing systems offer fast, flexible manufacturing. They require reliable connectors to facilitate, protect, and manage fluid flow from the beginning of the process to final fill-finish.

  6. The Case For Modernizing Small-Volume Aseptic Processing 9/2/2025

    Tube welding and biosafety cabinets present significant costs and risks for small-volume aseptic processing. Modern single-use aseptic connectors offer a more efficient alternative.

  7. A Tool For Rapid Quantification Of Nanoparticles 9/1/2025

    Traditional nanoparticle analysis creates process bottlenecks. Learn about an interferometric light microscopy method that provides accurate physical titer and size distribution from raw samples in under a minute.

  8. Conquering Challenges In Viral Vector Production 8/27/2025

    Scaling gene therapy demands precision and actionable data. Discover how integrated technologies like ultracentrifugation and mass spectrometry enhance AAV yield, purity, and characterization.

  9. Development Of RP Methods For The Analysis Of Synthetic Peptides 8/26/2025

    Explore the expanding role of synthetic peptides in drug development and learn how advanced RP chromatography methods are vital for impurity profiling to ensure safety and efficacy.

  10. Development Of Scalable Purification For Biotherapeutic Peptides 8/26/2025

    Discover key strategies for reversed-phase isolation of biotherapeutic peptides, as well as learn about method development, scale-up techniques, and RP/MS analysis to enhance purification workflows.