Veeva Disclosures

Veeva Disclosures facilitates the comprehensive management of sharing clinical trial study registrations and results with registries. It encompasses the entire process from data capture and review to workflow management, approval, reporting, and submission in XML format.

To enhance compliance, pre-configured registry rules simplify adherence to regulatory requirements. The platform's automated alerts keep users updated on changes in study data and critical milestones, prompting timely actions. In addition, the automatic filing of disclosure documents into electronic Trial Master File (eTMF) systems ensures proof of submission.

Insightful reports and dashboards allow users to monitor global submission statuses, track operational progress, and evaluate key metrics effectively. Integration with existing data systems like eTMF, Clinical Trial Management Systems (CTMS), and Study Startup eliminates the need for third-party integrations and reduces the likelihood of manual data entry errors.

Key Features and Benefits

• Speed Submissions: Expedite registry submissions using pre-configured rules and automated alerts for updates.
• Simplify Compliance and Oversight: Ensure accuracy and transparency with data validation, version control, and audit trails.
• Improve Efficiency and Agility: Boost productivity through real-time document authoring, easy configuration, and streamlined approval workflows.
• Unify Clinical Operations: Reduce dependencies on external systems with the reuse of data and documents.