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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Integrations

API:
Yes, Veeva SiteVault has an API
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Company Details

Company:
Veeva Systems
Headquarters:
United States
Website:
sites.veeva.com/products/sitevault-enterprise/

Media

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Product Details

Platforms
SaaS
Type of Training
Documentation
Live Online
Webinars
Videos
Customer Support
Online

Veeva SiteVault Features and Options

Scientific Data Management System (SDMS) Software

Analytics
Artificial Intelligence (AI)
Audit
Centralized Data Repository
Collaboration
Compliance
Data Security
ELN Integration
LIMS Integration
Workflows

Clinical Trial Management Software

21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning

Veeva SiteVault User Reviews

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