Veeva SiteVault
Veeva SiteVault empowers clinical research sites by streamlining operations and enhancing compliance. By replacing cumbersome paper processes with a secure digital platform, it allows for efficient management of regulatory and source documents. This centralized system facilitates real-time monitoring, accelerates study activation, and fosters collaboration among sponsors, sites, and patients.
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Top Veeva SiteVault Features
- Streamlined regulatory operations
- Real-time trial visibility
- Customizable workflows
- Secure document access
- Compliance with 21 CFR Part 11
- HIPAA compliance features
- Integrated sponsor system access
- Efficient study activation process
- Centralized document management
- Enhanced patient recruitment tools
- Collaboration with industry professionals
- User-friendly interface
- Detailed reporting and dashboards
- Automated document sharing
- Time-saving tracking features
- Reduced manual processes
- Improved operational efficiency
- Increased study quality
- Comprehensive training resources
- End-to-end demo availability
