Veeva Vault Platform
Regulated content and data management for clinical, quality and regulatory
What is Veeva Vault Platform?
Veeva Vault is a cloud platform for managing regulated content and data in life sciences. Applications built on it cover clinical operations (eTMF, CTMS), quality management (QMS, QualityDocs), regulatory information management, safety and promotional material review. Validated releases, audit trails and 21 CFR Part 11 controls support GxP compliance. It is used by pharmaceutical, biotech, medical device and contract research organisations.
Key facts
- Starting price
- Contact for quote
- Pricing model
- Quote-based
- Active users
- —
- Customers
- —
- Vendor employees
- —
- Launched
- 2011
- Deployment
- Cloud (SaaS)
- Platforms
- Web
Strengths & considerations
Strengths
- Unified platform for regulated content and data
- Strong compliance and validation support for life sciences
- Frequent cloud releases with new capabilities
Considerations
- Configuration can be complex across Vault applications
- Costs grow as more Vault applications are added
- Industry-specific focus limits broader use
- Pricing only on request
- No free plan or free trial
Editorial summary based on public information; not a user review.
Industries & use cases
Industries served
Typical use cases
- Clinical trial management and electronic trial master file
- Regulatory submissions and registration tracking
- Field rep engagement with healthcare professionals
Typical Deloitte services
- Vault implementation and data migration
- Clinical and regulatory operations redesign
- Commercial CRM transition and omnichannel engagement
Editorial profile based on public information.
Features
✓Workflow automation· Automation
✓AI features· Automation
✓File versioning· Documents
✓E-signature· Documents
✓API access· Integrations
✓Custom reports· Reporting
✓Dashboards· Reporting
✓Single sign-on (SSO)· Security
✓Role-based access· Security
✓Audit log· Security
User reviews
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