Veeva SiteVaultAre you a clinical research site?
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Research sites have long struggled with manual processes and technology solutions that were not built with their needs in mind. Veeva SiteVault simplifies investigator site file management by providing a single eRegulatory system to standardize their workflows across all their studies.
Veeva SiteVault eliminates the need to train and manage multiple site organizations and users by offering a solution that is fully supported by Veeva. 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
- 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.
