Veeva SiteVault Description
Streamline regulatory operations within your organization to improve compliance. Veeva SiteVault simplifies clinical trial management by connecting all regulatory operations. This improves efficiency and compliance. A single system that integrates regulatory and source documents supports 21 CFR Part 11 compliance and HIPAA requirements. SiteVault Enterprise provides real-time visibility across trials and speeds study activation. It also enables faster and more quality trial execution. To speed up study activation and reduce manual work, you can replace manual processes with your own workflows. Monitors will have secure, direct access into your source and regulatory documents. This will eliminate the need to redact or grant EMR access. You can create your own workflows, reports and dashboards to gain greater insight into regulatory processes and start-up timelines.
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