LSC Recent Webinars on BIO
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Driving Robust Tech Transfer In Biologics: CFD Simulation
11/12/2025
Computational Fluid Dynamics simulation is essential for robust biologics tech transfer. See how this predictive tool optimizes critical scale-up processes, reducing risk and expediting time to market.
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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.
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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.
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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.
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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.
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Achieve Pharma 4.0 With Next Generation Software-Defined Manufacturing
11/5/2025
Explore how software-defined manufacturing is helping companies overcome legacy system challenges, improve OEE by up to 25%, and accelerate batch release cycles while maintaining compliance.
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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.
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Faster Tech Transfers Through Seamless Digital Transformation
10/30/2025
Manual process documentation slows innovation. Learn how modular libraries and digital connectivity enable faster, error-resistant execution, bridging the gap between process design and automation.
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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.
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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.