Veeva Vault Clinical Data Management Suite
Veeva Vault CDMS is built for today’s clinical trials, eliminating technology limitations so you can design and run the trial you want. Innovative design tools speed the build process and eliminate manual steps. A next generation interface for data review helps CRAs work quickly and accurately and eliminates time spent paging through forms. Vault CDB, a clinical data platform for aggregation and cleaning, provides a complete and concurrent view across all your study data.
Run the Study You Want
Configure your casebooks for master protocols and adaptive trials with less time and effort. Make mid-study amendments with zero downtime and no migrations.
Get Clean Data Faster
Clean EDC data faster with a flexible interface that’s optimized for SDV and review. Reconcile data across multiple sources with a holistic view of all your study data.
Greater Visibility and Control Over Your Data
Gain visibility into your data, whether the study is managed internally or by CROs. Operational reports on the status of your data keep you informed throughout the study.
Veeva is delivering a better EDC that lets you run the trial you want. Vault EDC enables complex, multi-arm adaptive trials and allows mid-study design amendments without downtime. It is modern, agile, and fast – dramatically improving the user experience for sites, monitors, and data managers.Learn more
Vault Coder codes medical terms quickly and accurately within Vault EDC. In addition to auto-coding, synonym lists, and dictionary support for WHODrug and MedDRA, Veeva provides innovative ways to speed coding in batches and groups.Learn more
Veeva CDB assembles all your study data into a consistently formatted data lake for integrated cleaning, reporting, and export. Complete and current data helps you clean data faster, make better decisions, and run more effective trials. (Planned availability in late 2022)Learn more
To see a full list of available Vault Connections, visit the Veeva Development Cloud page.
Veeva RTSM supports multiple different randomization schemas to handle your most complex study designs. Flexible control over trial supply with advanced tools will minimize drug wastage.Learn more
Take Back Control of Your Studies
Tanya du Plessis, Bioforum
Evelyn Dorsey, Cara Therapeutics
Innovation that Redefines Traditional Processes
Veeva Vault CDMS provides modern agile systems that support the pace and complexity of today’s clinical trials.
Vertex’s second study with Veeva was built 50% faster than the 12 week corporate target
This top 20 pharma is standardizing on Vault CDMS enterprise-wide
Veeva reduced Cara Therapeutics’ typical database build time by 50%