LSC Webinars CELL All

  1. 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.

  2. 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.

  3. Streamlining Vaccine Purification: Techniques For Modern Modalities 9/23/2025

    Explore cutting-edge chromatography techniques accelerating vaccine purification across diverse modalities, with case studies on HPV, Malaria, and COVID-19.

  4. Advancing Non-Viral Gene Editing With Enhanced Post-Electroporation Performance 9/22/2025

    Non-viral gene editing is a powerful method for cell therapy. Learn how to address key challenges like cell viability and thermal damage with an innovative approach designed to improve performance.

  5. Mobilizing Science, Partnership, And Capability To Develop A Gene Therapy In 14 Months 9/17/2025

    Hear how one family, driven by urgency, partnered with AAV experts to develop a treatment for their daughter’s ultra-rare neurodegenerative disorder, NEDAMSS, in just 14 months.

  6. From Flow Data To GMP Decisions: How Express Modes Standardize QC 9/16/2025

    Standardizing QC in flow cytometry is now possible with embedded digital guidance. Discover how Express Modes help ensure consistency, compliance, and faster insight in cell and gene therapy workflows.

  7. Advances In Pediatric Transplant: T-Cell Depleted Haploidentical Experience 9/11/2025

    Explore how T cell–depleted haplo-HSCT is expanding donor options for pediatric patients, with insights into clinical outcomes, immune recovery, and evolving strategies.

  8. Real-Time Monitoring Of Higher-Order Structure Of RNAs 9/10/2025

    Learn how a new biophysical characterization strategy can enhance RNA therapeutic candidate screening and formulation development through a deeper understanding of RNA structure under native conditions.

  9. Extractables, Leachables, And Risk: Ensuring Safety In Pharma Manufacturing 9/8/2025

    This session is designed for teams developing new products, optimizing processes, or preparing regulatory submissions, and will provide practical tools for a better approach to E&L management.

  10. Solving Fragmentation: Future-Proofing The Advanced Therapy Supply Chain 9/5/2025

    Whether you are preparing for your first clinical shipment or scaling for global distribution, this conversation provides strategies to streamline operations, improve reliability, and deliver better patient outcomes.