Veeva Disclosures
Centralize and Streamline Clinical Trial Disclosures
Automate processes to ensure accurate, on-time submissions.
Announced 2023 Status Early Customers 1-10
See how unified systems simplify disclosure management
Overview
Reduce complexity and accelerate submissions with Veeva Disclosures
Manage disclosure processes
Veeva Disclosures manages the sharing of study registrations and results disclosures with registries. It supports the entire process, including capture, review, workflow, approval, reporting, and XML generation and submission.
Automate with rules and workflows
Pre-configured registry rules make it easy for users to comply with regulatory requirements. Automated alerts for changes in study data and milestones keep users informed about important tasks and prompt them to take action. Automatic filing of disclosure documents in Veeva eTMF helps generate proof of submission.
Get real-time visibility
Reports and dashboards provide visibility into global submission status, operational progress, and key metrics.
Leverage unified systems
Veeva Disclosures uses data from Veeva eTMF, Veeva CTMS, and Veeva Study Startup, eliminating third-party integrations and manual data entry.
