On-Demand Webinars

  1. Advancing Non-Viral Gene Editing With Enhanced Post-Electroporation Performance 9/22/2025

    Non-viral gene editing is a powerful method for cell therapy. Learn how to address key challenges like cell viability and thermal damage with an innovative approach designed to improve performance.

  2. Automated Active Microbial Collection In Aseptic Filling Lines 9/21/2025

    Learn how automated environmental monitoring strengthens contamination control strategies, reduces risk, and supports intervention planning in aseptic filling lines.

  3. It's Never Too Late To Intensify: Upstream Process Intensification 9/21/2025

    Explore how early upstream intensification, flexible facility design, and smart technology choices can reduce costs, improve scalability, and support sustainability in low-volume protein therapy production.

  4. Mobilizing Science, Partnership, And Capability To Develop A Gene Therapy In 14 Months 9/17/2025

    Hear how one family, driven by urgency, partnered with AAV experts to develop a treatment for their daughter’s ultra-rare neurodegenerative disorder, NEDAMSS, in just 14 months.

  5. Transforming Nanoparticles By Continuous Manufacturing 9/13/2025

    Discover how continuous manufacturing of nanoparticles can improve process efficiency, reduce costs, and increase the quality of the final drug product.

  6. Using Innovation To Accelerate And Optimize Your Scale-Up Strategy 9/10/2025

    Explore how AI, QbD, and digital transformation are reshaping manufacturing to accelerate scale-up, reduce defects, and optimize batch release for faster, more resilient operations.

  7. How Single-Use Technologies Are Simplifying Contamination Control 9/10/2025

    Learn how single-use technologies help reduce contamination risks and support compliance with updated EU GMP Annex 1 guidelines for aseptic processing and sterile drug manufacturing.

  8. Nanoforming Biologics, GLP-1s: From I.V. To Sub Q And Inhaled Delivery 9/9/2025

    Developing new delivery routes is essential for creating more effective treatments. Nanoforming enables new routes to simplify dosing, enhance patient comfort, and reduce healthcare costs.

  9. Operational Readiness In Pharma 9/9/2025

    Operational Readiness bridges project delivery and GMP manufacturing to ensure systems and teams are prepared for execution. Discover how a digital validation platform streamlines this transition.

  10. Modernizing CSV: How AI And CSA Are Changing The Game 9/9/2025

    Explore how life sciences companies are streamlining validation with AI and CSA principles. Learn practical strategies that boost efficiency, accuracy, and compliance—backed by real-world examples.