The field of cell and gene therapy is progressing rapidly, but significant manufacturing challenges persist. Key concerns include delivering safe, efficient, and potent cellular therapies affordably and promptly. The manufacturing process is complex, labor-intensive, and is prone to contamination risks and errors.
To address these issues, closed, automated cell processing systems with validated protocols using GMP-compliant raw materials are critical. In this webinar, industry experts will talk about efficient cell therapy manufacturing processes that aim to reduce contamination risks and cost of manufacturing. Data and a GMP closed process for the production of CAR-T cells utilizing a novel humanized CD19 lentiviral vector construct will be presented by Biocell Innovation. The webinar will also cover the importance of strategic industry partnerships in driving and fostering innovation and commercialization of cell therapies.
In this webinar, you will learn about: