R&D Demo Center
From R&D to clinical trials to quality and manufacturing, Veeva’s cloud-based content management applications are developed specifically for the global life sciences industry. See how different content management in the cloud can be by taking a look at the sneak peeks below, then be sure to contact us for more information.
Veeva Vault for Clinical Operations
Accelerate Trial Execution
Watch how Veeva Vault for Clinical Operations leverages the Vault platform to eliminate silos across CTMS, eTMF and study startup to streamline end-to-end clinical trial processes, accelerate trial execution, and deliver real-time visibility.
Streamline Document Collection, Management, and Analysis
Take a quick look inside Vault eTMF to see how sponsors and CROs are able to easily manage their clinical trials, as well as create comprehensive business reports, by utilizing a modern, cloud-based electronic trial master file solution.
Vault Investigator Portal
A Single Source for Sponsor, CRO and Investigator Collaboration
Vault Investigator Portal provides a two-way document exchange that places documents directly within the sponsor eTMF. Streamlined document management speeds study start-up and improves the efficiency of site communications.
Global visibility, Improved Data Quality, Better Informed Decisions
Vault Registrations provides a single global destination for planning, tracking and reporting on product registrations and health authority commitments. See how the improved visibility and data quality can streamline regulatory business operations.
Faster Submissions, Improved Collaboration, and Continuous Visibility
See how Vault Submissions makes it easy to dynamically build and track submission content and create powerful business reports. With Vault Submissions, collaborating throughout the development and approval process has never been so simple.