LSC Webinars CELL All

31. Accelerating Clinical Data Review Without Losing Control 6/25/2026

    Faster clinical review requires more than automation. See how governed AI can help teams spot issues sooner and preserve trust, transparency, and expert control throughout decision-making.

32. Global Regulatory Compliance For Aseptic Barrier Systems 6/24/2026

    Reconcile differing regulatory philosophies in sterile manufacturing. Learn to use prescriptive baselines and scientific data to achieve global compliance.

33. Building Scalable Non-Viral Gene-Edited Cell Therapy Processes 6/24/2026

    Rahul Purohit, Ph.D., discusses the challenges and opportunities of scaling non-viral gene-edited cell therapies, with practical guidance for balancing performance, cell quality, and manufacturing readiness.

34. Automating cell therapy manufacturing without redesigning established workflow 6/24/2026
35. Automating Cell Therapy Manufacturing Without Redesigning Workflows 6/23/2026

    Cell therapy manufacturing teams face mounting pressure to automate without disrupting workflows. Learn how incremental automation can preserve process integrity and reduce risk.

36. Smarter DNA, Healthier Cells 6/22/2026

    Standardizing cross-functional communication and unifying data architectures streamlines technology transfer, minimizes costly manufacturing deviations, and accelerates therapeutic scale-up.

37. How Intensified Upstream Processing Improves Scale-Up And Tech Transfer 6/22/2026

    Intensified upstream processing can improve scalability and maintain quality. Learn how automation, PAT, and data-driven control strategies help modernize workflows and support consistent performance.

38. Generate Stable High-Producing Clones In 14 Weeks 6/18/2026

    Rising complexity is putting pressure on cell line development. Discover a streamlined approach that enables rapid generation of stable clones with strong titers and long-term consistency.

39. Creative Chromatography Solutions For Complex Small Molecules 6/18/2026

    Chromatographic modeling enables smarter purification. Discover how digital tools, fraction mapping, and expert execution can improve yield for the most challenging small-molecule separations.

40. Using Residual DNA Quantification Data To De-Risk mAb Development 6/11/2026

    Residual DNA quantitation offers more than impurity measurement. When used across process steps, it helps compare purification performance, identify risks early, and ensure assays remain reliable.