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Unlocking Regulatory Efficiency with Veeva Vault Submissions Archive

Introduction to Veeva Vault Submissions Archive

Veeva Vault Submissions Archive is a powerful solution that serves as a secure, global repository for submission published output. This tool acts as the central hub for all applications submitted to health authorities, providing users with a comprehensive history of regulatory submissions. Launched in 2015, this product has reached a mature status and is trusted by over 100 customers globally.

Key Features and Functionality

One of the key features of Vault Submissions Archive is its dynamic search, filtering, and navigation capabilities. Users can easily sift through vast amounts of data to locate specific submissions or documents. The tool also includes a viewer that supports all electronic and paper formats, offering seamless navigation and visibility into submission structures. Moreover, the Active Dossier feature enables users to track the components that are currently active for any product and market combination.

Benefits and Impact

The impact of Veeva Vault Submissions Archive extends beyond mere efficiency gains. With over 15 of the top 20 companies utilizing Vault RIM, this solution has led to an 88% reduction in IT systems and a substantial decrease in written standards. Furthermore, users benefit from enhanced control over user access, streamlined tracking of health authority correspondence and commitments, and improved global readiness for regulatory submissions.

Customer Success Stories

Vault RIM has garnered trust from over 400 top and emerging biopharmaceutical companies. Customers like Mundipharma have experienced significant transformations in their regulatory operations by implementing Vault RIM. The Head of Regulatory Affairs at Mundipharma, Helen Donnelly, acknowledges the positive impact of this solution, stating that it has revolutionized the way regulatory functions are carried out within the organization.

Resources and Support

To aid users in maximizing the potential of Veeva Vault Submissions Archive, various resources are made available. These include comprehensive product sheets, informative case studies, end-to-end demos, best practice guides, and ebooks on successful RIM implementation. Additionally, Veeva offers support through its Connect platform, where customers can engage with product leaders and peers to exchange knowledge and insights.


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Streamlining GxP Content Management with Veeva Vault QualityDocs

Efficient GxP Content Management

Veeva Vault QualityDocs offers a robust solution for managing GxP content efficiently. With the ability to reduce effort by up to 90% through digital authoring, review, and approval processes, QualityDocs simplifies content management for quality teams. This regulated quality content management solution is built on Veeva's proprietary GxP content reference model, ensuring best practices and standardization.

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Enhancing Postmarket Surveillance with Veeva Vault Product Surveillance

Streamlined Postmarket Incident Reporting

Veeva Vault Product Surveillance (VPS) is a cutting-edge software solution designed to simplify and standardize postmarket incident reporting management for medical devices and diagnostics. By offering a seamless connection with quality and regulatory processes, VPS enables proactive complaints handling, which in turn accelerates continuous innovation throughout the product lifecycle. This streamlined approach not only improves product safety and reliability but also enhances overall quality standards.

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Optimizing Clinical Trials with Veeva Vault eTMF

Leading Trial Master File Application

Veeva Vault eTMF is a powerful solution designed to ensure the quality, timeliness, and completeness of a Trial Master File (TMF). This innovative platform offers enterprise content management capabilities, enabling seamless upload, version control, quality control, and approval of study documents. With real-time co-authoring features integrated with Microsoft Office, users can collaborate efficiently on essential documents like consent forms. The Veeva Vault eTMF application is highly efficient, robust, and supports global outsourcing requirements.

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Veeva Vault Platform: Revolutionizing Life Sciences Data Management

Introduction to Veeva Vault Platform

Veeva Vault Platform stands out as a cutting-edge solution tailored specifically for the life sciences industry. As the backbone for managing content and data seamlessly on a robust enterprise cloud platform, Veeva Vault unlocks a realm of possibilities for innovation and efficiency across both Research & Development (R&D) and Commercial sectors.

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Revolutionizing Clinical Trials with Veeva eCOA

Introduction to Veeva eCOA

Veeva eCOA stands for electronic Clinical Outcome Assessments, offering a modern solution to simplify the design, management, and completion of eCOA for sponsors, sites, and patients. This innovative platform announced in 2022 has already gained early traction with 11-50 customers benefiting from its advanced features.

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