Overview of Vault Submissions Archive
Veeva Quality Vault Submissions Archive is a revolutionary global repository that serves as the authoritative source for submissions sent to health authorities. This comprehensive solution allows users to access a complete history of regulatory submissions, including applications and health authority correspondences, in one secure location. With a dynamic search, filtering, and navigation system, users can easily locate and view submissions alongside all previously submitted applications. Additionally, the Active Dossier feature provides visibility into the submission components currently active for any product and market combination.
Key Features and Benefits
One of the key features of Vault Submissions Archive is its embedded document viewer that supports all electronic and paper formats, offering PDF link navigation for electronic submissions. Users can control user access, ensuring that the right content is shared with the right people based on configured business rules. The system also allows for the tracking of health authority correspondence and commitments, streamlining regulatory compliance processes. Moreover, organizations can maintain global readiness by enabling remote team members to access authorized submissions from anywhere in the world.
Customer Success Stories
Veeva Quality Vault Submissions Archive has been successfully implemented by over 100 customers, including top biopharmaceutical companies. Vault RIM, the underlying technology, is trusted by 400+ top and emerging biopharmas, showcasing its effectiveness in optimizing regulatory operations. Testimonials from customer success stories highlight the transformative impact of Veeva's solutions on regulatory affairs departments, with significant improvements in efficiency and compliance achieved.
Why Choose Vault Submissions Archive
Vault Submissions Archive offers unparalleled benefits to organizations aiming to achieve regulatory excellence. The system's dynamic search, filtering, and navigation capabilities ensure that users can easily access and manage their regulatory submissions. By centralizing submission data and providing secure access, organizations can streamline their regulatory processes while maintaining compliance with health authorities. Furthermore, the solution enables organizations to reduce written standards, consolidate IT systems, and enhance global readiness, ultimately leading to improved operational efficiency and regulatory compliance.