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
Benefits for sponsors and CROs