Upstream Manufacturing Webinars

31. The First On-Demand, Automated Solution For Powdered Media And Buffer Hydration 7/29/2026

    Discover how an automated, single-use hydration system cuts preparation time in half while delivering consistent, on-demand media and buffer solutions for bioprocessing operations.

32. Industry Highlights: Switching From Manual To Automated HSC Gene Engineering 7/28/2026

    See how automation can help make HSC gene therapy manufacturing more consistent, scalable, and efficient by reducing manual handling and improving key process outcomes such as transduction efficiency.

33. Future-Focused Customer-Centric Bioprocessing Solutions With Eppendorf 7/24/2026

    De-risk bioprocess scale-up with application-focused workflow validation. Discover strategies for transitioning therapies from R&D to clinical production.

34. Enhancing AAV Manufacturing Yield Via Mini-Helper Plasmid 7/23/2026

    Learn how rational plasmid engineering and promoter optimization can significantly improve AAV productivity while reducing plasmid burden, paving the way for more efficient and scalable viral vector manufacturing.

35. Navigating AI Compliance In Life Sciences: FDA Policy Insights For AI Governance 7/22/2026

    Navigating life sciences AI compliance requires strong governance, expert human oversight, and transparent, low-risk deployment strategies.

36. Leveraging 3Rs For Superior Cell Line Characterization 7/13/2026

    Explore how non-animal methods, including next generation sequencing, are advancing biologics safety testing through the 3Rs while supporting faster adventitious virus testing and more.

37. Large-Scale Lentivirus Manufacturing With A Transfection Complex Stabilizer 7/6/2026

    De-risk large-scale lentivirus manufacturing by mastering transfection complex stability. Find out how to control particle aggregation, reduce fluid volumes to 2%, and minimize expensive GMP costs.

38. Trusted Performance With A Plus: Seamless Transfer From R&D To Commercial 7/5/2026

    Bridge the gap between early R&D and commercial biomanufacturing. Learn how scalable control architectures, automated gassing strategies, and digital validation protocols streamline tech transfers.

39. Optimize Every Step In Your Biopharma Site 7/5/2026

    Bridge the gap between validation and cleanroom execution. Learn how proactive site surveys, residue management, and robust CAPA programs resolve compliance deficiencies and ensure audit readiness.

40. Streamline Fluid Disconnections And Reduce Tear-Down Complexity 7/5/2026

    Accelerate process turnover and fortify fluid line sterility without complex tools. Gain insight into how modern, metal-free connector geometries mitigate spillage and preserve cell viability.