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Thermo Fisher Scientific
Preparing for an evolving regulatory landscape to successfully commercialize cell and gene therapies
Webinar On Demand
Cell and gene therapies are progressing through clinical trials and driving towards commercialization at a rapid pace. As a result, regulatory agencies have had to pivot quickly to provide guidance to support the pace of development.
Based on extensive experience supporting early-stage and clinical-stage companies through the drug development and approval process, the webinar will provide critical guidance for navigating regulatory requirements to accelerate the commercialization process and get much-needed therapies to patients sooner.
Listen to this webinar to hear industry expert, Monica Commerford, Ph.D.