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.