LSC Recent Webinars on BIO

  1. Cleanroom Conceptual Design Paradigm: Converting Spaces For GMP Operations Part 2 6/16/2025

    Learn essential conceptual design principles for transforming alternative spaces into efficient, regulatory-aligned cleanroom environments for your critical processes.

  2. Unlocking Efficiency In Large-Scale Microbial Manufacturing 6/16/2025

    Gain insights into how expert teams and the right tools help build resilience into manufacturing systems and tackle small, often-overlooked issues before they become costly problems.

  3. The Role Of Developability In Lead Candidate Selection 6/12/2025

    Discover how developability assessments are crucial for identifying biologic candidates that are both effective and manufacturable, thereby reducing risks and improving the chances of clinical success.

  4. Seals And Stability: Preventing Failures In Synthesis And Chromatography Columns 6/11/2025

    Unlock the key to long-term column performance and stability. Learn how crucial seal maintenance can prevent catastrophic failures and safeguard your therapeutic products.

  5. Optimizing The Progression Of Biotherapeutic Candidates To FIH Studies 6/9/2025

    Learn actionable strategies that can lead to higher success rates and smarter resource investment, paving the way for a successful path to IND submissions and commercialization.

  6. Advanced Contamination Control: Automation, Assays, Process Efficiency 6/5/2025

    Learn how automated closed systems and larger bioprocess containers contribute to maintaining product integrity and how rapid analytical assays can offer reliable and accurate contamination detection.

  7. Optimize Your Advanced Therapy Manufacturing Process Before You Automate 6/5/2025

    Dive into specific unit operations and case studies that demonstrate how implementing phase appropriate tools can have substantive direct business impacts to cost and development timelines.

  8. A New Look At Subcutaneous mAb Delivery Using Nanoformed Particles 6/3/2025

    A highly concentrated non-aqueous suspension of an IgG1 was developed using a patented platform. Review how the particle size of the mAb impacts the overall behavior of the drug product.

  9. Peptones And Vaccines: A Synergistic Approach To Enhanced Production And Efficiency 6/2/2025

    Enhance your vaccine manufacturing with peptones. Explore their benefits, analyze data-driven productivity gains, and learn integration strategies in this informative, on-demand session.

  10. Building A Purification Toolkit For An Expanding Variety Of mAb Therapeutics 5/29/2025

    Explore techniques for optimizing purification toolkits for various monoclonal antibody formats. This session covers resin and buffer selection for efficient downstream process development.