On-Demand Webinars

  1. Genomic Medicine At An Inflection Point 9/1/2026

    In vivo therapies and streamlined ex vivo manufacturing are redefining genomic medicine. Understand the tradeoffs, priorities, and technical challenges influencing how future treatments are designed.

  2. A Practical Roadmap For Column Sizing, System Selection, And GxP Readiness 9/1/2026

    Chromatography scale-up depends on aligning different factors. Learn which factors can help maintain process consistency, manage risk, and support the transition from development to manufacturing.

  3. Faster Paths To Biosimilar Equivalence: Turning Guidance Into An Advantage 9/1/2026

    Evolving biosimilar guidance creates opportunities to reduce comparative clinical requirements through strong analytical evidence, risk-based justification, structure-function knowledge, and more.

  4. Chromatography Polishing In The Age Of Intensification 9/1/2026

    As upstream processes intensify, chromatography polishing must handle higher loads and evolving impurity profiles. Modern strategies can improve clearance, extend resin life, and maintain throughput.

  5. How Perfusion In Seed Train Bioreactors Can Simplify Upstream Processes 9/1/2026

    N-1 perfusion achieved approximately 95% viability while scaling from bench to production. See how this approach intensified seed trains without affecting subsequent fed-batch performance.

  6. Improved Clearance Of Host Cell Proteins After Virus Inactivation 9/1/2026

    Learn how post-viral inactivation filtration can support precipitate and host cell protein removal while balancing throughput, purity and cost across different feeds and process development conditions.

  7. QMSR Is Done. Now What? 9/1/2026

    Align with FDA QMSR requirements by integrating ISO 13485 standards, moving quality management upstream, and tracking process health metrics to ensure continuous regulatory compliance.

  8. What To Expect In The Next Revision Of IEC 62304 9/1/2026

    Prepare for updates to IEC 62304 by learning how revised process rigor levels and expanded health software scopes impact medical device software development and compliance.

  9. Using Computational Fluid Dynamics To Design Scalable Processes 8/31/2026

    Learn how CFD modeling and experimental data can be combined to assess power input, mixing, oxygen transfer, and more across bioreactor scales, supporting sound process decisions.

  10. Driving Optimization Through Connected Laboratory Environments 8/31/2026

    Discover how connected laboratory data and predictive modeling can strengthen process control, improve yield, and more, creating a faster and more resource-efficient approach.