LSC Webinars CELL All

  1. Advancing Next Gen Antibodies: From AI Driven CLD To Manufacturing 6/2/2026

    See how growing ADC complexity is driving the adoption of AI-enabled, data-driven CMC strategies that accelerate development, improve product insight, and strengthen manufacturing readiness.

  2. Challenges And Opportunities With Novel AAV Capsids 6/2/2026

    Explore challenges and solutions in developing novel AAV capsids, focusing on manufacturing complexity, analytical testing, and regulatory considerations for advancing gene therapy effectiveness.

  3. CAR-T Strategy In 2026: Scaling Autologous, Advancing Allogeneic 5/29/2026

    As CAR-T advances, shifting clinical progress and market dynamics are reshaping development strategies. Explore how evolving therapies and operational demands are redefining the next wave of innovation.

  4. Quality By Design: The Future Of Automated Pharmaceutical Labeling 5/28/2026

    Learn how applying Quality by Design principles to automated labeling platforms utilizes robotics to eliminate manual errors and seamlessly adapt to future pharmaceutical packaging formats.

  5. In Vivo CAR-T And Gene Editing: Manufacturing Reality Behind The Promise 5/27/2026

    Gain practical insights into the manufacturing realities shaping in vivo CAR-T development and learn how leading teams are addressing the challenges of scaling both LNP and viral vector platforms."

  6. Real-Time DAR And Concentration Measurement Without Dilution 5/27/2026

    Maintaining consistent DAR while reducing risk and variability remains a major ADC challenge. Learn how real‑time spectroscopy replaces dilution‑heavy workflows and strengthens process control.

  7. Advancing Therapeutic Discovery With High-Throughput Electroporation 5/21/2026

    Learn how high-throughput electroporation streamlines genetic material delivery for cell therapy and drug discovery, offering speed, precision, and scalability across hard-to-transfect cell types.

  8. The Framework For Containment In A Cleanroom 5/20/2026

    ISO classification decisions shape cleanroom design. Learn how early alignment between process needs, biosafety, and classification can reduce redesign risk while supporting scalable environments.

  9. Understanding The Regulatory Landscape For Ophthalmic Drug Products 5/14/2026

    Learn how evolving ophthalmic regulations, contamination control strategies, and advanced packaging solutions can help support compliance, product quality, and patient safety.

  10. AI Meets Informed Consent: Opportunity, Risk, and What IRBs Need to See 5/14/2026

    Expert perspectives on IRB oversight, health literacy, and research ethics offer practical guidance to strengthen consent, protect participants, and align compliance with real-world research.