Veeva Vault CDMS
Looking for clinical operations
Veeva Vault CDMS eliminates the need for multiple tools with a single clinical data management application that combines coding, EDC, data cleaning, and reporting. Companies can now manage study build through execution on a single application.
The ability to manage all trial data, including non-CRF, dramatically improves visibility during a trial. With a complete and concurrent view of their data, clinical development teams can make better decisions faster.
* Vault Data Workbench is planned for availability in late 2019.
- Complete and current data: Gain transparency and visibility to all clinical data for both local and remote (CRO) trials.
- Accelerate study cycle times: Deploy studies in days, not weeks and improve time to database lock with a flexible, formless view of your data that is better for cleaning and monitoring.
- Simple and cost efficient: Replace multiple applications with one solution, reducing the burden of data integrations for clinical trials.
- Unify clinical: Part of a comprehensive suite that includes Vault CDMS, Vault CTMS, Vault eTMF, and Vault Study Startup.
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Veeva Vault EDC
Vault EDC is part of Veeva Vault CDMS. It provides a fast and intuitive interface for capturing clinical trial data. Designed for flexibility, Vault EDC allows you to run complex multi-arm adaptive trials and make mid-study amendments without downtime or migrations. Veeva is delivering a better EDC that lets you run the trial you want.
AGILE DESIGN STUDIOVault EDC provides a configurable collaboration environment with built-in review and approval workflows. Users can build casebooks with easy drag-and-drop functionality.
DATA-DRIVEN PERSONALIZATIONPersonalized user dashboards and workflows provide immediate direction of users’ tasks and minimize time spent searching for information. The role-based user interface optimizes the order and structure of data differently for data entry, data cleaning, and monitoring to provide the ideal view for each activity.
ENDPOINT-DRIVEN STUDY DESIGNEndpoint-driven study design provides the ability to optimize collection, verification, cleaning, and formatting of study data based on prioritization. Site monitoring and data management are improved with a shared data model, enabling risk-based approaches to study execution.
BEST IN CLASS PLATFORMA scalable platform that has the flexibility to amend designs at any stage without downtime or migrations.
MODERN USER EXPERIENCEA modern user experience greatly increases usability, adoption, and performance. During data entry on a form, real-time edit checks increase accuracy, entry performance, and user satisfaction. The quick-jump navigation reduces time spent navigating between subject casebooks, events, and forms.
SEAMLESS CONNECTION TO CTMSEasily leverage operational data from Vault EDC for reporting within Vault CTMS. CTMS users can report on the status of subjects and dates captured in Vault EDC, as well as navigate to a subject’s casebook in Vault EDC.
Veeva Vault Coder
Map highly variable free text entries or “verbatims” to standard coded terms based on MedDRA or WHODrug dictionaries. Vault Coder, a part of Veeva Vault CDMS, lets you code clinical form verbatims for data on trial medications, adverse events, prior surgeries, medical histories, and more.