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Unlocking Regulatory Excellence with Veeva Quality Vault Submissions Archive

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.


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Maximizing Efficiency and Compliance with Veeva QualityDocs

Streamlined GxP Content Management

Veeva QualityDocs offers a robust solution for quality teams to efficiently manage GxP content. With the ability to reduce effort by up to 90% through digital authoring, review, and approval processes, this platform streamlines document management tasks.

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Ensuring Global Product Quality with Veeva Vault Product Surveillance

Streamlining Postmarket Incident Reporting

Veeva's Vault Product Surveillance (VPS) software offers a streamlined and standardized approach to managing postmarket incident reporting for medical devices and diagnostics. By harmonizing global postmarket surveillance processes, VPS simplifies the reporting of incidents, ultimately enhancing product safety, reliability, and quality. This tool enables companies to maintain a high standard of product quality while ensuring compliance with regulatory requirements.

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Revolutionizing Quality Management in Manufacturing with Veeva Quality Suite

Modernizing Manufacturing Quality

Veeva Quality Suite is transforming manufacturing quality by bringing increased visibility, efficiency, and control to Contract Development and Manufacturing Organizations (CDMOs) and Generics. This modern solution revolutionizes how R&D and Quality leaders connect and collaborate to drive excellence

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Boost Trial Efficiency with Veeva Quality Vault eTMF Solution

Leading Trial Master File Application

Veeva Vault eTMF stands out as the top choice for managing trial master files to ensure quality, timeliness, and completeness. It offers comprehensive enterprise content management capabilities that allow for seamless upload, version control, QC, approval, and real-time co-authoring with tools like Microsoft Office. This enables study document management, including consent forms, to be highly efficient and reliable while supporting global outsourcing needs.

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Streamline GMP Decisions with Veeva Vault Batch Release

Facilitate GMP release and market-ship decisions

Veeva Vault Batch Release is a comprehensive solution designed to streamline GMP release and market-ship decisions by automating the aggregation, reviews, and traceability of batch-related data and content. This streamlines the process, enabling faster and more confident decisions, ultimately speeding up time-to-market and reducing costs. By bringing together data and content from various sources like QMS, LIMS, ERP, and Vault RIM, Vault Batch Release simplifies collaboration with external partners, making the entire process more efficient.

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