On-Demand Webinars

  1. When A Logbook Project Becomes A Digital Movement 12/11/2025

    A leading pharma company accelerated execution and compliance in GMP operations. See how modular apps replaced manual processes, setting a new foundation for continuous innovation.

  2. Seal The Deal: Mastering Vent Integration In Medical Devices 12/9/2025

    Learn how precise vent placement and microfiltration design optimize performance in life science devices. See practical troubleshooting strategies and a real-world case study.

  3. Lessons From FDA 483s And Warning Letters: Cleanroom Compliance 12/8/2025

    Learn critical lessons from FDA 483 observations and Warning Letters to proactively address common GMP cleanroom compliance failures and build an inspection-ready facility.

  4. Eliminate Risk From Your Viral Vector Tech Transfers 12/5/2025

    Explore strategies to simplify viral vector tech transfers, reduce risk, and maintain quality under tight timelines, as well as a case study that demonstrates how to streamline this critical process.

  5. Navigating Innovation And Challenges In CGT Bioprocessing 12/4/2025

    This expert panel breaks down the practical realities of today’s supply chain while forecasting how emerging technologies will redefine quality standards.

  6. Navigating Regulatory Expectations For Injectable Packaging 12/4/2025

    Explore insights on extractables, focusing on how they relate to the revised EU GMP Annex 1, new and evolved expectations under USP <382>, and the use of VHP decontamination in aseptic environments.

  7. Unlock Productivity In mAb Production: Upstream And Downstream Intensification 12/3/2025

    Boost your mAb manufacturing efficiency by mastering upstream and downstream intensification strategies. Learn how to minimize cost and time while increasing overall productivity.

  8. Critical Path For Gene Therapy: AAV Analytical Lifecycle Considerations 12/2/2025

    Explore considerations for phase-appropriate AAV characterization and release activities from pre-clinical to late-phase products. Review validation challenges and paths for maturation of analytics.

  9. Model-Driven Genetic Design And Bioprocess Optimization Across Modalities 12/2/2025

    Traditional biomanufacturing relies too heavily on trial and error. By integrating AI and mechanistic models into early design, developers can overcome productivity limits and accelerate timelines for complex therapeutic modalities.

  10. Raising The Bar In Gene Therapy 12/1/2025

    Learn how a science-driven and digitally structured approach reduced onboarding timelines for gene therapy from 12 months to just 3, setting a new benchmark in technology transfers.