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Webinar | Roadmap to Market for Cell and Gene Therapies

October 12, 2020

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Nothing is standard about the study design, study conduct or the regulatory process in cell and gene therapy trials. Every cell and gene therapy is different due to the specific characteristics of each product, with a complicated regulatory approval process and unique therapeutic challenges.

 

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Webinar | Reducing Study Build Time from Weeks to Days

October 1, 2020

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Study start-up and post-go-live protocol amendments can be lengthy, costly, and disruptive to a clinical trial. But with the right technology, data managers can accelerate timelines and overcome these challenges.

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