Bio-Expo Live Upstream Bioprocessing

  1. Simplifying Custom Media From Development To GMP With An End-To-End Approach 11/6/2026

    Custom media manufacturing across US and European sites, paired with rapid prototyping of proprietary formulations as a scale-down model, shapes how teams move cell culture processes toward GMP production.

  2. Between The Samples: Seeing Cell Culture As It Happens 11/3/2026

    Periodic sampling can miss transient metabolic shifts in cell expansion. Time-resolved glucose and lactate profiles help define candidate process parameters, and those parameters then inform decisions about automated culture operations.

  3. Rev Up AAV Production: Optimized Transfection Solutions To Start Strong 11/3/2026

    Transfection sets the ceiling for usable AAV at harvest. Optimizing the reagent system and complex stability raises titer and percent full capsids across serotypes, cell lines, and bioreactor scales.

  4. The Hidden Variables Shaping Bioprocess Reproducibility 11/3/2026

    Discover how advanced benchtop bioreactors and automated control strategies eliminate hidden process variables to ensure consistent bioprocess reproducibility.

  5. Functional Gaps In Structural Biology: Evolving EPR For Modern Biology Labs 11/3/2026

    A compact, automated pulsed EPR design now moves distance-based functional readouts of biomacromolecules into the wet lab, without expert operators or cryogen refills.

  6. Control With A Plus: A New Tool To Improve Your Bioprocess Runs 11/3/2026

    Reproducibility becomes more consequential as a process scales from development to manufacturing. Replicate-CHO runs test how consistently one controller maintains process parameters, growth, metabolism, and antibody yield.

  7. Large-Scale Lentivirus Manufacturing With A Transfection Complex Stabilizer 7/6/2026

    De-risk large-scale lentivirus manufacturing by mastering transfection complex stability. Find out how to control particle aggregation, reduce fluid volumes to 2%, and minimize expensive GMP costs.

  8. Trusted Performance With A Plus: Seamless Transfer From R&D To Commercial 7/5/2026

    Bridge the gap between early R&D and commercial biomanufacturing. Learn how scalable control architectures, automated gassing strategies, and digital validation protocols streamline tech transfers.

  9. Optimize Every Step In Your Biopharma Site 7/5/2026

    Bridge the gap between validation and cleanroom execution. Learn how proactive site surveys, residue management, and robust CAPA programs resolve compliance deficiencies and ensure audit readiness.

  10. Streamline Fluid Disconnections And Reduce Tear-Down Complexity 7/5/2026

    Accelerate process turnover and fortify fluid line sterility without complex tools. Gain insight into how modern, metal-free connector geometries mitigate spillage and preserve cell viability.