On-Demand Webinars
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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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Accelerating Process Scale-Up From Benchtop To Commercialization- From Controller To Software
11/4/2025
Discover strategies for optimizing process control, refining media selection, and ensuring safety through rigorous contaminant detection to mitigate development risks.
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Innovations, Solutions, And USP <1062> With Scale Up
11/4/2025
Optimize tablet compression by simplifying calibration, speeding up changeovers, and utilizing advanced laser inspection to prevent critical punch tip wear and maintain quality.
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Supply Chain Efficiency And Sourcing In Gene Therapy
11/4/2025
An overview of the inbound supply chain in gene therapy and the process development challenges that are frequently faced. Learn about concepts such as scaling, cell culture media sourcing, mixing technologies, and configurable packaging.
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Basic Cell Culture Education Series: CHO Media
11/4/2025
This Knowledge Culture Basic Education Series on CHO media will explore CHO cells: their lineage, historical culture media, and process improvements. We will dive into how to optimize cell culture performance for superior outcomes.
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The Evolution Of GMP Asset Management
10/31/2025
Learn how teams are shifting from reactive maintenance to predictive intelligence with connected systems, real-time insights, and AI-driven asset strategies while keeping compliance at the center.
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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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How To Address Your Solid Dosage Processing Needs
10/27/2025
Unlock the keys to consistent solid dosage products. Learn to align unique product needs with optimal processing requirements and equipment strategies. Gain a roadmap for improved quality and reproducibility.
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Smarter CMC Strategies To Accelerate Next-Gen Biologics To The Clinic
10/23/2025
Learn how process design and cross-functional collaboration mitigate risks and accelerate the path from early development to FIH manufacturing through real-world case studies of practical approaches.