Veeva SiteVault

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SiteVault enables clinical research sites to save time and accelerate research by streamlining the management of regulatory documents and processes in a modern eRegulatory system.

Veeva SiteVault simplifies investigator site file management by providing a single eRegulatory system to standardize regulatory documents and processes to speed study execution.

With capabilities such as electronic signatures, remote monitoring, certified copy workflows, and reporting, sites have access to a modern cloud solution to streamline trial activities, accelerate clinical research, and improve collaboration across sites, sponsors, and CROs.

Benefits for research sites

  • Reduce administrative burden: Increase efficiency by standardizing regulatory documents and processes
  • Speed study activation: Streamline reviews and approvals to speed study activation and enroll patients sooner
  • Increase visibility: Gain real-time visibility into document status to improve compliance and oversight

Benefits for sponsors and CROs

  • Be the sponsor of choice: Improve site satisfaction by arming them with an eRegulatory solution that is built specifically for their needs to use across all their studies, regardless of what technology their sponsors use.
  • Improve collaboration: Streamline document and data sharing with sites by helping to build a network that will change the way information is exchanged in clinical research.
  • Streamline monitoring: Improve the monitoring experience and gain visibility into investigator files for greater oversight.

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