Intensification of mAb Downstream Processing with Full Membrane Chromatography Workflow
Wednesday, November 5, 2025
Session 1: 10 a.m. CET | 1:30 p.m. IST | 4 p.m. HKT
Session 2: 8 a.m. PST | 11 a.m. EST | 5 p.m. CET
In protein-based therapies, the demand for efficient and flexible manufacturing processes is increasing due to their potential to reduce costs of goods, enable wider drug accessibility, increase capacity, and reduce process footprint. Manufacturers have started to leverage single-use facilities and advancements in upstream processing to drive process intensification — and while this has increased mAb titers, it’s also amplifying productivity bottlenecks downstream and driving the need for chromatography process intensification.
This webinar presents a lab-scale study and a scale-up model that can predict the cost and productivity benefits of implementing a full membrane chromatography workflow for mAb purification, from process development to GMP commercial manufacturing. The speakers will demonstrate how membrane chromatography can purify large amounts of antibodies faster, with fewer consumables, and in a smaller facility footprint, all while meeting the product quality attributes.
What You Will Learn:
- Explore the benefits of process intensification (PI) and how to ensure successful implementation
- Anticipate PI challenges and solutions when transitioning to intensified processes
- Discover cost-modeling tools for implementing a full membrane chromatography process