Thermo Fisher Webinars

31. 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.

32. AAV Purification: Solving Downstream Challenges 6/9/2025

    In this roundtable discussion, a trio of distinguished experts in AAV purification and process development share their expertise and best practices in tackling and solving downstream challenges.

33. CAR-T Strategy In 2026: Scaling Autologous, Advancing Allogeneic 5/29/2026

    As CAR-T advances, shifting clinical progress and market dynamics are reshaping development strategies. Explore how evolving therapies and operational demands are redefining the next wave of innovation.

34. Efficient Scale-Up Of Monoclonal Antibody Production: From Bench Top To 500L 8/11/2025

    Scaling monoclonal antibody production from the lab to a commercial scale can be challenging. Learn about an approach that helps you maintain consistent productivity and product quality across all scales.

35. 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.

36. Development Of A CHO Medium And Feed System Using Advanced Analytical Tools And Workflow Considerations 6/16/2025

    Discover how multiomics analysis and optimized formulations in a new cell culture medium deliver higher protein titers and specific productivity for CHO fed-batch systems.

37. Leveraging dPCR r Techniques To Quantitate Lentivirus Particles 5/28/2025

    Discover how digital PCR can streamline lentiviral vector characterization to reduce variability and improve analytical sensitivity. Learn how this approach can help you comply with regulatory guidance.

38. Supporting Development Of mRNA Therapeutics By Enabling Commercial-Scale mRNA Purification 6/9/2025

    Discover the next generation of scalable affinity capture for high-quality mRNA purification. Learn how a simple, reliable binding mechanism can maximize efficiency and simplify your manufacturing process.

39. Innovative Strategies For Residual DNA And Viral Titre Quantitation 5/22/2025

    Discover how digital PCR improves the accuracy of residual host cell DNA and viral titre quantification in biotherapeutic manufacturing to enhance product quality, safety, and regulatory compliance.

40. Manufacturing Considerations For Viral & Non-Viral Platform Selection 6/24/2025

    In this webinar, a panel of experts spanning the lentiviral vector, exosome and oncolytic virus fields will discuss the impact of manufacturing considerations on their respective platform selection and ongoing product/process development strategies.