On-Demand Webinars

  1. Contract Manufacturing: Must-Know Trends And Strategies For 2025 2/12/2025

    Regulated industries face rising demand, tech breakthroughs, and regulatory harmonization. Discover how contract manufacturers must leverage AI and cloud solutions to stay agile and compliant in the future.

  2. Essential Considerations For Selecting The Right Biologic Fill/Finish Partner 2/12/2025

    Partnering with a provider that prioritizes quality and yield optimization not only ensures product safety but also helps reduce operational costs.

  3. Purity As A Priority: Optimizing Safety Measures For rAAV Therapies 2/11/2025

    Watch to learn how rAAV vectors in gene therapy are addressing manufacturing impurities, risks to patient safety, and analytical methods for detection while aiding sponsors in regulatory compliance.

  4. LBA Vs. LC-MS: Competing Technologies At A Development Crossroad 2/6/2025

    Watch as bioanalytical experts Shane Karnik, MS, and Matt Hartle, Ph.D., explore why many sponsors are reevaluating the use of LBA for large molecule protein analysis in favor of LC-MS.

  5. Scaling Up For Cell And Gene Therapies 1/31/2025

    Explore cutting-edge bioreactor strategies and overcome the challenges of large-scale production, including hydrodynamic conditions, media costs, and process reproducibility.

  6. Scalable Expansion And Downstream Processing Of High-Quality hiPSCs 1/31/2025

    Learn about a scalable, microcarrier-based 3D culture process for expanding hiPSCs to 10L, yielding over 10 billion cells while maintaining quality.

  7. The Next Frontier In mRNA: Modular Manufacturing For Scalable RNA-LNP Therapies 1/29/2025

    Explore constructing a modular RNA-LNP GMP facility using Cytiva's FlexFactory™ process train in a KUBio™ environment to scale RNA-LNP therapies.

  8. Linking mAb Product Quality Profile Changes To Your BioProcess: A Case Study 1/23/2025

    Optimize your bioprocess and product quality with high-frequency data. Discover how to streamline mAb characterization and link process changes to product attributes.

  9. Quality Roundtable: Raw Material Planning For Tech Transfer And Scaling Biologics 1/22/2025

    Join this roundtable of biopharmaceutical professionals as they share their insights to help you navigate important quality and planning decisions for the progression of your biologic.

  10. Growing A Sustainability Culture Across An Expanding CDMO Network 1/15/2025

    Peter Skals, Head of Global Sustainability, shares how the company is integrating its climate and ESG strategy while simultaneously expanding its CDMO network and reducing its CO2 footprint.