Veeva Vault CTMS
Looking for clinical data management solutions? Click here

Veeva Vault CTMS is the only modern cloud application that makes it easy for life sciences companies to unify clinical information and processes, streamline trial management, and gain complete visibility across the trial portfolio.

Clinical study teams enjoy an easy to use, consistent experience with a single sign-on and have one source for clinical master data and study information. Organizations can manage the entire end-to-end clinical trial process and gain a global view into tasks and processes, all in one unified, secure, and reliable system.

With one seamless system of record and simple navigation across clinical trial processes, Vault CTMS improves operational efficiency and enables faster, higher-quality trial execution.

BENEFITS
  • Faster trials: Equip study teams with easy to use role-based dashboards and streamlined navigation to improve productivity and speed trial execution.
  • Better decision making: Enable proactive closed-loop issue management and improve strategic trial planning with a complete real-time view of trial status.
  • Streamlined clinical operations: Provide one seamless system of record for shared CTMS, TMF, and study start-up content, improving efficiency and streamlining operations.
Read More
CTMS-Main-screenshot

Features

STUDY PLANNING AND VISIBILITY
Plan and track study milestones across trial-related activities to optimize trial resources and to proactively plan for events such as aligning clinical supply arrival with site initiation visit or assessing site performance across studies.
TRIAL CONDUCT
Assess progress on activities such as site management, by monitoring and subject enrollment against goals, identify sources of delay, and take corrective action to restore momentum.
SITE MONITORING
Document and identify trends on site adherence to ICH/GCP guidelines. Confirm study is conducted in accordance with the protocol from anywhere on any device. Implement a remote monitoring strategy to reduce your number of site visits, track and resolve issues in real-time.
SINGLE SOURCE OF TRUTH
Leverage the same trial content and data across Vault eTMF and Vault Study Startup. Submit trial information and documentation once and leverage it across different systems, sites, and countries.
SINGLE SOURCE FOR CLINICAL MASTER DATA
Ensure high quality data across clinical applications with one system of record for master study, study country, and study site information.
ROLE-BASED DASHBOARDS AND REPORTS
Create easy, self-serve reports showing documentation and information by any combination of attributes including: portfolio, study, region, country, investigator, site activation status, and more.
Easy to Use
Study teams work more efficiently with simple, easy to use navigation and workflows across business processes, improving productivity and accelerating study execution
DYNAMIC SECURITY
Maintain proper controls and security by providing levels of access based on study team or role, reducing overall risk and improving quality.
optimize for your trial
Streamline operations with a flexible, agile solution that is easily configured to your organization’s unique clinical trial needs, study designs, therapeutic areas, and business processes.

Demos & Videos