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Webinar: Rewriting the Code: Advances and Challenges in Pediatric Gene Therapy
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Pediatric gene therapy is rapidly transforming treatment for rare genetic diseases. Join Dr. Rachel Abu Taleb as she explores AAV, lentiviral, and CRISPR platforms, reviews lessons from approved therapies, and examines the scientific, regulatory, and access challenges shaping future innovation. Learn how these advances are redefining care and improving outcomes for children with rare diseases. Click here to learn more.
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Video | Invetech
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One continued challenge for scalable commercial cell therapy manufacturing is closing and automating the entire process. Many core processes may be closed, but peripheral systems remain vulnerable.
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Video | Cell & Gene
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Expert panelists Pratik Jaluria, Ph.D., SVP TDS at BlueRock Therapeutics, Bruno Marques, Ph.D. VP, P&PD at Century Therapeutics, and Kate Rochlin, Ph.D., COO at IN8bio, discuss best practices for translating lab development processes into cGMP manufacture settings.
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Webinar | MaxCyte, Inc.
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Unlock superior non-viral CAR T manufacturing outcomes by combining gentle microbubble T cell isolation with advanced electroporation. See how this approach boosts cell viability and transfection efficiency.
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Webinar | MilliporeSigma
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Discover how next-generation sequencing and targeted bioinformatic pipelines characterize encapsidated DNA to provide a clearer picture and ensure vector consistency and safety.
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Webinar | Andelyn Biosciences
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Finding partners with the necessary skills to optimize AAV processes is crucial for minimizing risk. Explore key considerations for advancing your therapy from concept to commercialization.
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Video | Cell & Gene
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This segment features Omkar Kawalekar, Ph.D., M&SC Lead, Deloitte Consulting, and Zoe Zheng, ED, PTS Lead, Legend Biotech, discussing the innovations most likely to impact CGT commercialization, such as closed automated platforms, AI-driven analytics and predictive release, and digital orchestration.
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