From clinical study conduct to sign-off: Modernizing Site Collaboration

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Disconnected document workflows create avoidable delays during clinical trial monitoring and closeout. Join us to see how Box can streamline document exchange and monitoring throughout study conduct, so sponsors, CROs, and sites can prepare for visits, collaborate securely, and distribute study media with clear visibility into site acknowledgement.

USDM Life Sciences helps life sciences organizations maximize the value of Box through validated workflows, compliance-focused implementation, AI governance, and continuous Cloud Assurance. During this webinar, we’ll explore how Box and USDM enable secure, compliant clinical site collaboration, streamlined approvals, and inspection-ready study execution.

Topics we’ll cover:

AI-assisted monitoring: Prepare for visits, classify documents, and streamline source review with AI
Digital sign-off: Deliver end-of-study media digitally and track site acknowledgement
Governed collaboration: Securely exchange documents across sponsors, CROs, and sites
Operational visibility: Reduce follow-up and track document status across monitoring and closeout

Speakers

Manu Vohra

Managing Director, Life Science, Box
Lekha Nelavelli

Product Manager, Box
Najiba Baig

Validation Engineer, USDM