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Discover how Box transforms life sciences study startup by centralizing regulated and non-regulated content into a single, GxP-validated platform. This session will demonstrate how automated workflows and templates for Trial Master Files (TMF) and investigator site files eliminate manual handoffs to accelerate study timelines. Join us to learn how to reduce compliance risk and improve time-to-market through secure, seamless collaboration across your entire clinical ecosystem.
Speakers
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Manu VohraManaging Director, Life Science, Box
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Allison StilleySr. Solutions Engineer, Box
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Scott PicancoSenior Product Marketing Manager,
Box