Veeva SiteVault

Veeva SiteVault Enterprise is an eRegulatory / eISF system that streamlines and scales site regulatory operations to improve compliance and advance clinical research. Manage regulatory and source documents in a single system that supports 21 CFR Part 11 and HIPAA requirements. With a real-time visibility across trials, SiteVault Enterprise improves operational efficiency, speeds study activation, and enables faster, higher-quality trial execution.

• Speed Study Activation: Replace manual processes and design one's own workflows to support quality and speed study activation.
• Enable Remote Monitoring: Eliminate the need to grant EMR access or redact documents by providing monitors with secure, direct access to regulatory and source documents.
• Enhance Visibility and Flexibility: Create one's own workflows, reports, and dashboards for greater visibility into start-up timelines and regulatory processes.