Cytiva webinars and podcasts

1. Sterilizing-Grade Filtration Of mRNA Encapsulated Lipid-Nanoparticles 9/2/2026

   Compare sterilizing-grade membrane performance at high and low pressures, including throughput, bacterial retention, and the effects of filtration on particle diameter and encapsulation efficiency.

2. Role Of Membrane Chemistry And Filter Format In TFF 9/2/2026

   Compare hollow fiber and flat sheet TFF formats across three membrane chemistries, and see how filter selection can influence ambient-temperature UF/DF optimization, processing time, and quality.

3. Enhancing mRNA-LNP Downstream Processing Via Single-Pass TFF 9/2/2026

   Single-pass tangential flow filtration effectively concentrates mRNA-LNPs and removes ethanol while maintaining quality. See how this approach produced LNPs with 4.2-fold higher in vitro potency.

4. Accelerate Your pDNA And mRNA Process Development 11/13/2025

   Explore a structured approach to optimizing and scaling plasmid DNA production using E. coli, with insights into key growth parameters, benchtop feasibility, and pilot-scale performance.

5. Developing Your Risk-Based Approach To Single-Use System Integrity 10/29/2025

   Explore how a holistic approach to single-use system integrity can strengthen contamination control, improve operational efficiency, and meet evolving regulatory expectations in manufacturing.

6. Scaling Up Your E. Coli pDNA Process From Parameter Screening To Pilot Scale 6/26/2025

   Discover a systematic approach to scalable plasmid DNA production using E. coli OneShot Top10, which features DOE-driven optimization and key insights for efficient biomanufacturing success.

7. All Biopharma Roads Begin With Eco-Design: How Can You Get Started? 11/20/2024

   Listen to a discussion between Ryan Walker, Cytiva, and Aude Arkam, Sanofi, to learn how the influence of eco-design can guide sustainability in the biopharma industry.

8. Scope 3 Emissions: Cut The Complexity With Creative Collaboration 11/20/2024

   Delve into the crucial role of Scope 3 emissions in the biopharma industry's sustainability journey, and learn more about the challenges and opportunities of managing these types of emissions.

9. Innovations In Perfusion Bioprocessing 11/7/2024
10. How To Plan For Trouble-Free Filter Validation 10/28/2024

    Watch to learn when filter validation should be performed, what is required from an end user and laboratory testing perspective, and how to achieve first-time success for various drug products.