Choose Site
Veeva US
Veeva EU
Veeva CN
Veeva US

Modern content management applications built in the cloud.

Veeva delivers regulated content management applications for every major part of a life sciences company, from R&D, to clinical trials, to quality and manufacturing. Companies in pharma, biotech, and medical devices are replacing their legacy systems with Veeva’s modern applications built in the cloud. The results are happier users, dramatic process improvements, and reduced regulatory risk.

Veeva R&D Applications

Veeva R&D applications are built on the Vault Platform, the only modern cloud platform built for regulated content management. Each application includes deep functionality to meet the needs of a specific business process. From an electronic trial master file that study teams like to use, to an enterprise-wide quality system that scales globally, Veeva Vault delivers best practices with unprecedented ease.

Vault eTMF brings sponsors, CROs, and investigator sites together in the regulated cloud. Sponsors get complete visibility with real-time dashboards and actionable reports. CROs get a smart eTMF that tracks outstanding content and automatically places documents into the eTMF. The result is complete visibility, faster study start-up, and an inspection ready eTMF.
Learn More | Launch Demo

Vault Investigator Portal helps sponsors and CROs get off paper and maintain an audit-ready eTMF. The interface is simple - just documents and tasks. The backend is powerful - autofiling into the eTMF when relevant documents are exchanged. And since Veeva’s portal provides a direct interface to Vault eTMF, companies get better reporting and visibility into study status.
Learn More | Launch Demo

Vault QualityDocs provides a single global source for quality and manufacturing SOPs, reports, and validation documents. Vault makes managing quality documentation easy: there’s real-time collaboration without downloading documents. Secure unfettered access for external partners. Ensure easy fulfillment of training requirements with “Read & Understood” tracking.
Learn More | Launch Demo

Veeva delivers regulated content management applications for every major part of a life sciences company, from R&D, to clinical trials, to quality and manufacturing.

Vault Submissions unites contributors, partners, and affiliates in the cloud with a single destination for regulatory documents. Create global and regional submission dossiers to harmonize the planning process and provide real-time visibility into submission readiness.
Learn More | Launch Demo


Vault MedComms provides an efficient way to manage global medical communication content. A common repository supports easy collaboration and version control, and an open API allows integration and accurate fulfillment across all communication channels and geographies.
Learn More | Launch Demo


Vault Platform is the technology foundation delivering security, performance, and configurability to all Veeva Vault applications. Vault Platform also provides an extensive portfolio of compliance capabilities to help customers manage regulated documents and high-value content of all types. Learn More

Services Team

Customer success is our top priority, which is why the Services team finds people with deep life sciences experience and technology expertise and provides extensive training on Veeva products. Learn More