Clinical trial analytics · Veeva Systems
Veeva Vault CDMS
Unified EDC and clinical data management application built on Veeva's Vault platform for life sciences.
Veeva Vault CDMS combines electronic data capture (EDC), coding, data cleaning, and reporting in a single application built on Veeva's Vault content and data platform, rather than stitching together separate EDC, coding, and cleaning tools. It aggregates data from sites, labs, ePRO/eCOA vendors, and RTSM systems into one environment, and shares its underlying Vault architecture with Veeva's clinical operations (CTMS), eTMF, and safety products, so operations and data management teams work from shared study metadata. Like Medidata and Oracle Clinical One, it is a system that runs the trial's data collection, distinguishing it from analytics-only layers such as Saama that sit over already-captured trial data. Vault CDMS targets pharmaceutical and biotech sponsors and CROs operating under GCP, 21 CFR Part 11, and HIPAA-aligned controls, and is sold as part of Veeva's broader Vault Clinical Suite.
At a glance
| Vendor | Veeva Systems |
|---|---|
| Pricing model | Quote only |
| Free tier | No |
| Deployment | Cloud |
| Open source | No |
| Best for | Sponsors already standardized on Veeva's Vault platform who want EDC and data cleaning in the same system as clinical operations. |
Pricing
Sold by subscription per study/application as part of Veeva's Vault Clinical Suite; pricing is quoted directly by Veeva.
Pricing has not been verified yet — see the vendor's site.
Features
- Unified EDC, coding, and data cleaning in one application
- Shared Vault metadata with CTMS and eTMF products
- Automated edit checks and query management
- RTSM and ePRO/eCOA data integration
- Role-based review and sign-off workflows
- Real-time reporting and study dashboards
- 21 CFR Part 11-aligned audit trail
Profile last reviewed September 21, 2026