Efficiently Managing Regulatory Dossier Lifecycle
Veeva Vault Submissions Archive is a cutting-edge solution designed to streamline the management of the regulatory dossier lifecycle. With this tool, organizations can access a comprehensive record of all regulatory submissions, creating a centralized repository for critical documentation. By maintaining a complete history of submissions, users can easily track the evolution of each application and ensure compliance with regulatory standards.
Comprehensive Repository of Submission Published Output
Vault Submissions Archive serves as a global and secure repository that houses all submission published output. It acts as the definitive source of applications that have been submitted to health authorities, offering organizations a robust platform for managing critical documentation. Users can leverage the viewer, which supports a wide range of electronic and paper formats, with convenient PDF link navigation for electronic submissions.
Enhanced Visibility and Accessibility
One of the key features of Vault Submissions Archive is its ability to provide enhanced visibility and accessibility to regulatory documents. Users can effortlessly view submissions, health authority correspondence, and all previously submitted applications in one centralized location. The embedded document viewer offers a detailed look into the structure of each document, facilitating easy navigation and understanding.
Empowering Global Regulatory Readiness
Vault Submissions Archive empowers organizations to maintain global regulatory readiness by allowing remote team members to access authorized submissions from anywhere in the world. This capability ensures that teams can collaborate effectively and stay compliant with regulatory requirements, even in a distributed work environment. By consolidating submissions from regional offices and local affiliates, organizations can ensure a cohesive approach to regulatory compliance.
Optimizing Efficiency and Performance
With Vault Submissions Archive, organizations can optimize efficiency and performance in regulatory compliance management. Dynamic search, filtering, and navigation tools enhance user experience, making it easy to find and retrieve relevant information. By simplifying submission tasks, saving time on approval processes, and consolidating legacy systems, organizations can achieve impressive results, with 80% of submission tasks eliminated or simplified, over 200 hours saved on approval and renewal reporting, and 65 legacy systems consolidated.