Streamlining Clinical Trial Disclosures with Veeva Vault Disclosures

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Streamlining Clinical Trial Disclosures with Veeva Vault Disclosures

Centralize and Streamline Clinical Trial Disclosures

Veeva Vault Disclosures is a powerful solution that centralizes and streamlines the management of clinical trial disclosures. By automating processes, this platform ensures accurate and on-time submissions, reducing the burden on research teams and improving overall efficiency. With an early status announcement for 2023, Veeva Vault Disclosures is already making waves in the industry.

Automate with Rules and Workflows

Vault Disclosures simplifies compliance with regulatory requirements by automating processes through pre-configured rules and workflows. Users can easily manage study registrations and results disclosures with support for capture, review, approval, reporting, and XML generation. Automated alerts keep users informed about changes in study data and milestones, ensuring prompt action when necessary.

Real-Time Visibility and Unified Systems

With Veeva Vault Disclosures, users gain real-time visibility into global submission status, operational progress, and key metrics. The platform leverages data from Vault eTMF, Vault CTMS, and Vault Study Startup, eliminating the need for third-party integrations and manual data entry. By centralizing data and document management, Veeva Vault Disclosures simplifies processes and enhances efficiency.

Why Choose Vault Disclosures

Veeva Vault Disclosures offers a range of benefits to streamline disclosure management. From global disclosures that are centralized to automated submissions with pre-configured rules, this platform accelerates the submission process. Additionally, users can simplify compliance and oversight, improve efficiency and agility, and unify clinical operations by eliminating the need for third-party integrations.

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