LSC Webinars CELL All

  1. Practical Solutions For Protein Analytics And Residual DNA Testing 11/12/2025

    Discover practical solutions for common quality control bottlenecks in biotherapy manufacturing. Learn how to improve protein analytics and DNA testing robustness and accelerate time to market.

  2. Choosing The Right Sporicide: Critical Factors For Robust Cleanroom Contamination Control 11/10/2025

    Choosing the best sporicide for your cleanroom involves evaluating factors like surface format, contact time, and safety. Learn the criteria to select an effective and robust agent for contamination control.

  3. Boosting Vaccine Yields Through Smarter Cell Culture Media Optimization 11/10/2025

    Unlock efficient vaccine production by understanding how tailored peptone supplementation optimizes cell culture media, improving cell growth and overall yield across multiple critical cell lines.

  4. Navigating Commercial Cell Therapy Manufacturing 11/7/2025

    Explore expert insights on manufacturing strategies, quality management, scalable production, and digital tools that enhance collaboration and ensure consistent, efficient multi-product facility operations.

  5. Driving Sustainability In Bioprocessing With Biobased Single-Use Solutions 11/7/2025

    Discover how biobased materials in bioprocessing enable measurable carbon emission reductions. Learn practical strategies to meet decarbonization goals and adopt greener, operationally sound practices.

  6. Enhancing Viral Vector Sterile Filtration: Process Efficiency And GMP Alignment 11/4/2025

    Explore filtration strategies that improve viral vector yield and quality, with insights on AAV and lentivirus workflows, plus practical guidance for implementing PUPSIT in line with requirements.

  7. How To Select The Right Bioanalysis CRO For Your Program 11/3/2025

    The right bioanalysis CRO accelerates progress, while the wrong one can derail outcomes. When every provider claims speed and credibility, how do you confidently choose the right partner?

  8. Developing Your Risk-Based Approach To Single-Use System Integrity 10/29/2025

    Explore how a holistic approach to single-use system integrity can strengthen contamination control, improve operational efficiency, and meet evolving regulatory expectations in manufacturing.

  9. Optimize DNA Clearance In High-Salt, GMP-Grade Purification Processes 10/28/2025

    Explore how salt-active endonucleases overcome DNA clearance challenges in viral vector purification by digesting down to 3–5 nucleotides and performing reliably in high-salt conditions.

  10. The Case For Optimized And Excipient GMP Cell Culture Solutions 10/27/2025

    Learn how optimized, customizable formulations and Excipient GMP manufacturing streamline development, ensuring quality and consistency for a de-risked path to the clinic.