Historically, tools that were developed for gene therapies have been repurposed for cell therapy monitoring; however, they have limitations including repeated validation requirements, limited assay sensitivity and suboptimal quantitative accuracy.
TORONTO (PRWEB)
February 01, 2023
Last March, the U.S. Food & Drug Administration (FDA) issued updated guidance related to cell therapy characterization, manufacturing and monitoring. Historically, tools that were developed for gene therapies have been repurposed for cell therapy monitoring; however, they have limitations including repeated validation requirements, limited assay sensitivity and suboptimal quantitative accuracy.
In this webinar, attendees will dive into the FDA’s latest cell therapy guidance and learn how a single-cell assay combined with high-throughput T-cell receptor (TCR) sequencing can provide a next generation solution for characterizing and tracking cell therapies.
Register to gain more insight into next-generation tools for cell therapy characterization, manufacturing and monitoring.
Join Alex Dahmani, Director, Immune Medicine, Adaptive Biotechnologies and Vincenzo Di Cerbo, PhD, Lead Scientist, Cell and Gene Therapy Catapult, for the live webinar on Wednesday, February 22, 2023, at 11 a.m. EST (4 p.m. GMT).
For more information, or to register for this event, visit Next-Generation Tools for Cell Therapy Characterization and Monitoring.
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Email: vkovacevic@xtalks.com
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