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Webinar: Building Scalable Non-Viral Gene-Edited Cell Therapy Processes
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Discover practical strategies for scaling non-viral gene-edited cell therapies from early development to GMP-ready manufacturing. This webinar explores electroporation-based workflows for T, NK, and CD34+ cells, including CRISPR knock-out, knock-in, and transposon delivery. Learn how to balance editing efficiency with viability, expansion, and downstream process needs while optimizing scalable, closed-system manufacturing approaches for long-term success in cell therapy development. Click here to learn more.
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Video | Thermo Fisher Scientific
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Explore proactive supply chain strategies designed to mitigate risk, maintain stringent quality standards, and satisfy global raw material demands amid evolving bioprocessing challenges.
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Video | Andelyn Biosciences
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Review data from an adherent manufacturing platform utilized for over 450 Phase 1 and 2 clinical batches, spanning 17 years of production across diverse serotypes and indications.
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Webinar | Invetech
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Discover how automation, modular design, and real-time analytics are transforming cell and gene therapy manufacturing to unlock scalable, cost-effective production without compromising quality.
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Video | Charter Medical
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Learn how single-use manifolds can optimize your biomanufacturing processes, reducing time, space, and resources while increasing flexibility, product quality, and scalability.
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Video | Cell & Gene
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In episode 129 of Cell & Gene: The Podcast, Host Erin Harris reconnects with Zachary Roberts, M.D., Ph.D., EVP of Research & Development and Chief Medical Officer at Allogene Therapeutics, to explore how allogeneic CAR-T is evolving from a scalability promise into an earlier-line, potentially curative intervention.
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Video | Contec, Inc.
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Ensure cleanroom compliance by aligning disinfectant validation with real-world application methods. Justify your protocols and adapt to facility changes through expert technical insights.
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