Vault Clinical Suite for CROs
Contract research organizations (CROs) are making significant advancements to modernize and speed clinical trials. Findings from recent research show CROs have taken decisive action to streamline trial execution by adopting new digital strategies and technologies that eliminate information silos, replace manual processes, and enable trial collaboration.
Vault Clinical Suite transforms clinical operations and clinical data management with the most comprehensive suite of clinical solutions, offering EDC, coding, data management, study start-up, eTMF, CTMS, and payments.
Strategic PartnerDeliver high-quality, differentiated
services to sponsors
Speed and AgilityBetter meet aggressive
EfficiencyReduce complexity and streamline
Veeva’s connected Vault Clinical Suite enables companies to take a unified approach to
clinical operations and clinical data management.
The Vault CDMS to Clinical Operations Connection enables bi-directional data flows to:
- Simplify monitoring
- Track and plan recruitment more effectively
- Pay sites faster
- Centralize deviation management
- Streamline reporting
Speed Study Start-up
Improving study start-up times requires a multi-pronged approach. Find the right sites, activate, and greenlight them faster with process automation. De-risk your timelines using Agile Design technologies and processes that speed study builds.
Productized Rules and Dynamics
Build studies quickly regardless of complexity
Document everything that was built and what changed without lifting a finger
Built-in Global Intelligence
Easily manage regulatory complexities with country-specific start-up workflows
Configuration not Code
Define range checks, date comparisons, and progressive display with simple configurations
Data-driven Site Selection
Select quality sites based on historical performance, reducing downstream monitoring costs and burden
Manage and prioritize critical tasks and milestones to keep study start-up on track
Be More Agile
Unified product suites, modern architectures, and a common technology platform make you more nimble and able to support growth with scalable operations. Respond quickly to sponsors’ requests for advanced trial designs and frequent post-production changes.
Easy Updates Mid-study
Make amendments without data migrations or EDC downtime for sites
Near-zero Custom Functions
Replace burdensome custom functions with a powerful rules engine that’s easy to use
Easily create new studies to accelerate engagements with sponsors
Increase Efficiency and Compliance
Vault Clinical Suite helps organizations go digital with their clinical processes and achieve a step change in productivity gains. Automating tasks removes manual steps, builds quality into your trials from the beginning, and increases compliance so you’re always inspection-ready.
Finish SDV faster with QuickView filters that help CRAs focus on what matters most
Milestone changes in study start-up and CTMS trigger automatic document filing in eTMF
Reuse master trial, site, and investigator data across studies to eliminate redundancy
Subject visits from EDC automatically trigger payable items, speeding payments
CRAs can view key study details at-a-glance and quickly author trip reports, saving time and money
Risk-based Study Management
Focus on critical risks and allocate resources effectively with study-level risk assessments and scoring in CTMS
Streamlining collaboration and information sharing with sponsors is a top priority for CROs looking to expand beyond tactical engagements. Providing timely, consistent information and visibility across studies helps build credibility and develop long-term strategic relationships.
Collaborative Design Reviews
Sponsors review the EDC system, not PDFs and spreadsheets, with many fixes made in real-time
Centralized Reports and Dashboards
Clients have real-time, self-serve access to reports that you’ve configured
Seamless Information Sharing
Automated information exchange enables better collaboration and faster trials
How can Veeva help your organization?
Contact an Expert