LSC Recent Webinars on BIO

  1. Simplified Harvest And Media Exchange In Cell Therapy 1/28/2026

    Scale-up often introduces shear stress and process variability. Learn how low-shear, single-use technology stabilizes media exchange and harvest, ensuring consistent cell quality and predictable performance.

  2. Next-Level Cell Lines: An Integrated Approach To Biologic Innovation 1/22/2026

    See how AI-driven tools and optimized platforms are accelerating biologics development, delivering high-titer clones in weeks, and paving the way for integrated design of cell lines and genetic systems.

  3. Five Practical Considerations To Move From Concept To Clinic 12/17/2025

    Learn more about five key factors for advancing targeted in vivo LNP programs, from formulation and targeting strategies to bioanalytical readiness and scalability.

  4. Overcoming Regulatory Hurdles In AAV Production 12/16/2025

    Demonstrating residual reagent clearance is a critical regulatory requirement in AAV manufacturing. Explore how specialized assays and strategic partnerships streamline compliance.

  5. From Lab To Commercialization: Simplifying Bioprocess Scale-Up 12/16/2025

    Explore how unique cuboid geometries and advanced mixing dynamics create consistent performance from the bench to commercial manufacturing, ensuring flexibility and improved productivity.

  6. Bridging The Gap Between Product Readiness And Equipment Availability 12/15/2025

    Discover how manual precision at scale bridges packaging gaps, accelerates product launches, and ensures uninterrupted supply to deliver quality when automated equipment isn’t yet operational.

  7. Automating Visual Inspection Qualification 12/11/2025

    Transferring visual inspection data from paper to digital is essential for Pharma 4.0 compliance. Learn practical strategies to eliminate errors, automate data tracking, and enhance quality assurance.

  8. 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.

  9. 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.

  10. 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.