LSC Webinars CELL All

  1. Evolving Gene Editing For Rare Disease Drug Development 10/9/2025

    Explore how scalable gene editing platforms are advancing therapies for ultra-orphan conditions, with insights into manufacturing models, regulatory strategies, and clinical approaches.

  2. Cell Bank And Scale Up Strategies For MSC And Exosome Manufacturing 10/9/2025

    Discover how effective cell banking and scale-up strategies can reduce risk and cost in advanced therapy manufacturing. Learn practical ways to meet increasing cell and exosome quantity needs.

  3. Compliance To Confidence: Annex 1 For Small-Batch, High-Value Production 10/3/2025

    Get strategies for meeting the updated GMP Annex 1 in small-batch aseptic filling. Learn about contamination control, quality management, and equipment design for high-value liquid and powder products.

  4. Supply Resiliency For Bioprocessing Amid Global Volatility 10/2/2025

    Build bioprocessing resiliency with strategic supply chain management. Learn to meet quality, compliance, and time-to-market demands amid global volatility with effective sourcing.

  5. Achieving Flexibility In T Cell Manufacturing - Adaptation Of Standardized Processes 10/2/2025

    Explore how scalable CAR-T manufacturing impacts T cell biology and therapy efficacy, as well as how standardized processes can support diverse production needs while preserving critical characteristics.

  6. Genetically Modified MSCs For The Treatment Of GvHD 9/30/2025

    Discover how genetically engineered MSCs are significantly advancing GvHD treatment. Learn about preclinical success with CXCR4-IL10-MSCs and the process for scaling up their GMP production.

  7. Avoid The Wrecking Ball: Targeted Solutions For Struggling Trials 9/30/2025

    In this presentation, our expert panel introduces the concept of scaffolding — a targeted reinforcement strategy designed to strengthen trials from the inside out.

  8. Filtration Unfiltered: Technology To Meet New Bioprocessing Challenges 9/29/2025

    Explore how filtration strategies are adapting to diverse molecule pipelines, regulations, and sustainability targets with insights into process intensification and the technologies shaping the future.

  9. How Digital Cleaning Validation Can Simplify Audit Readiness And Improve Compliance 9/26/2025

    Discover how to enhance audit readiness and improve compliance by shifting to a digital cleaning validation program. Learn to determine worst-case products and maximum safe carryover limits.

  10. Ensuring Compliance In Gene Therapy Trials: IRB And IBC Views 9/23/2025

    Explore ethical and regulatory challenges in neurological gene therapy trials, with expert insights on IRB/IBC collaboration, consent protocols, and oversight for vulnerable populations.