Wednesday, November 11, 2015: 8:30 AM
Ballroom B (Salt Palace Convention Center)
Multi-column continuous chromatography has recently become an enabling technology that will “break the bottleneck” in downstream processing of bio-pharmaceuticals. This development is not only driven by the tremendous increases in expression levels in the upstream fermentations, especially for monoclonal antibodies, but also by the introduction of biosimilars/biobetters the market. Continuous chromatography has shown promises in reduction of manufacturing cost. However, up to today there has not been a reported case at the production scale. What are the remaining technical barriers when implementing the technology in the GMP environment? This presentation highlights how to overcome the major barriers when developing this technology platform.
See more of this Session: Innovations in Biopharmaceutical Discovery, Development and Manufacturing
See more of this Group/Topical: Pharmaceutical Discovery, Development and Manufacturing Forum
See more of this Group/Topical: Pharmaceutical Discovery, Development and Manufacturing Forum