LSC Webinars

  1. Growing A Sustainability Culture Across An Expanding CDMO Network 1/15/2025

    Peter Skals, Head of Global Sustainability, shares how the company is integrating its climate and ESG strategy while simultaneously expanding its CDMO network and reducing its CO2 footprint.

  2. Demystifying Large Scale Continuous Chromatography For Small Molecules 12/18/2024

    Learn the fundamentals of developing a continuous chromatography process with Simulated Moving Bed (SMB) technology for small molecules, from gram-scale to multi-ton commercial production.

  3. Project Delivery Methodology To Accelerate Operational Readiness 12/11/2024

    Learn how to implement a focused operational readiness model that goes beyond traditional construction and startup schedules. Discover how this approach can reduce timelines and improve project success.

  4. Uncovering The Root Cause Of Clinical Trial Troubles 12/10/2024

    Discover essential strategies to prevent clinical trials from reaching a crisis while gaining a deeper understanding of the importance of addressing systemic issues early.

  5. Navigating Primary Packaging Challenges, Solutions For Emerging Innovators 12/5/2024

    If you are in the process of developing a complex or sensitive injectable drug, learn about containment solutions to mitigate your risks and help you get your drug to the patient faster.

  6. Leveraging Platform Processes For Developing And Accelerating Novel Gene And Cancer Therapeutics 12/5/2024

    Explore how platform processes advance gene therapies, the impact of strong partnerships on patient access, and the future shaped by these collaborations.

  7. Removing The Headache: Outsourced Stability Storage And Testing Solutions 12/4/2024

    Should you manage certain operations internally or partner with a trusted external provider? Watch experts discuss the benefits of outsourcing stability, storage, and testing.

  8. Charting A Successful CMC Journey For Your ADC Drug Product 12/3/2024

    These real-world case studies highlight best practices and strategies to optimize bioconjugate drug product tech transfers and supplies in the clinical or commercial phase.

  9. Early Preclinical Development: A Successful Transition To cGMP Manufacturing 12/2/2024

    Explore the development steps that lead to an mRNA construct optimized for your requirements and that meets future-proof cGMP manufacturing requirements, thereby de-risking the development.

  10. How To Boost AAV Titer With Feed Supplementation In Both HEK293 And Sf-9 Platforms 11/25/2024

    Explore how optimizing post-transfection or post-infection feeding in HEK293 and Sf-9 cells significantly boosts AAV titers, enhancing production efficiency for gene therapy applications.