Downloads

31. 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.

32. Extrusion-Based ASD Scale-Up: Ensuring Performance Through Process Understanding 9/30/2025
33. Automated Immunoassay For AAV Capsid Titer Measurement 9/30/2025

    Explore how automated immunoassays outperform ELISA in AAV quantitation—offering better sensitivity, precision, and matrix interference management to help you identify the best media for high viral titers.

34. Accelerate Analysis Of Titer, Process Impurities, And Process Contaminants 9/30/2025

    Learn how automated immunoassay platforms can accelerate titer and impurity analysis in AAV and LV vector workflows—reducing hands-on time while improving consistency from development through manufacturing.

35. Used Kikusui 36 Station Pharmaceutical Tablet Press: AQUARIUS G-J 9/30/2025

    Used Kikusui tablet in tablet press, model Aquarius G-J/DC, 36 station, keyed upper punch guides, B tooled, 100 kN pre-compression, 100 kN main compression, 16mm max tablet diameter, 18mm max depth of fill, rated up to 259,200 tablets/hour, with DC module for core feeder, 4-15mm core depth adjustment, with integrated primary and secondary powder feed hoppers, and core feed hopper, project# 1-6302, built 2009.

36. Rethinking MES In Pharma: Faster Reviews, Better Data, Less Risk 9/30/2025

    Discover how composable MES helps pharma teams scale faster, enforce SOPs, and maintain data integrity—while empowering frontline teams to build workflows that fit their operations.

37. Streamline Defect And Nonconformance Management 9/30/2025

    Track and manage defects and non-conformances – such as SOP deviations or missing data – from identification to resolution.

38. Accelerate Batch Releases With Right-First-Time Execution 9/30/2025

    Enforce standardized workflows while collecting data in real time, giving you the visibility you need to prevent deviations, review exceptions, and release batches faster.

39. Utilizing Flow Cytometry For Humoral Immunogenicity Testing: Cell & Gene Therapy 9/29/2025

    Discover strategies to overcome immunogenicity challenges in cell and gene therapies, with a focus on harnessing flow cytometry to enhance ADA and NAb assay development, strengthen validation, and ensure regulatory readiness.

40. Optimizing Aseptic Processing With Isolator Technology 9/29/2025

    Discover how pharmaceutical isolators optimize operations, achieve higher sterility assurance, and meet stringent regulatory requirements. Learn about design principles, validation, and VHP cycles.