LSC Recent Webinars on BIO
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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.
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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.
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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.
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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.
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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.
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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.
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Accelerate And Enhance Biomanufacturing Operator Training
5/28/2025
Unlock the power of blended operator training and learn how combining digital tools with hands-on instruction reduces errors, boosts retention, and empowers your workforce for real-world production success.
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Maximizing Media Strategies: Expert Insights On Boosting Performance
5/22/2025
Optimize biopharma media strategies for consistent protein quality. Experts discuss formats, variability, and actionable analytics in this on-demand virtual roundtable.
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Navigating Regulatory Shifts: EU GMP Annex 1 And USP 382
5/20/2025
Strengthen risk mitigation strategies while ensuring regulatory alignment. Gain valuable insights into best practices and proactive approaches for building a robust and future-ready CCS.
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Optimizing Biotherapeutic Protein Expression With CHO Vector Technology
5/19/2025
Review the development of a high-strength synthetic gene promoter that enhances titers while maintaining exceptional product quality and expression stability, to support more efficient biomanufacturing.