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Products-Veeva Vault

Revolutionizing Product Development with Veeva Vault

Unified Suites for Streamlined Efficiency

Veeva Development Cloud, offered by Veeva Systems, serves as the technological foundation for product development in various industries, especially the life sciences sector. This innovative solution aims to eliminate data and process silos across critical areas such as clinical operations, quality management, regulatory compliance, and safety protocols. By centralizing content and data on a single cloud platform, Veeva facilitates seamless collaboration and information sharing among global departments, leading to enhanced efficiency and regulatory compliance.

Key Benefits of Veeva Development Cloud

One of the primary advantages of Veeva Development Cloud is its ability to drive faster time-to-market for new products. By enabling consistent, end-to-end business processes on a unified system, organizations can increase operational efficiencies and accelerate product development cycles. Moreover, Veeva's solution promotes global alignment by providing visibility across headquarters, sites, and countries, ensuring that all stakeholders are on the same page throughout the development lifecycle. Another key benefit is the comprehensive compliance framework offered by Veeva, which ensures the reliability and quality of information across all stages of product development.

Trusted by Industry Leaders

Veeva Development Cloud is trusted by more than 450 biopharma, contract manufacturers, generics, and medtech companies globally. Industry leaders rely on Veeva's suite of applications to streamline their product development processes, enhance collaboration among cross-functional teams, and leverage data-driven insights to drive innovation. Testimonials from customers highlight the transformative impact of Veeva's cloud-based software on their operations, enabling them to work more collaboratively and efficiently.

Customer-Centric Approach and Support

Veeva's commitment to customer success is evident in its comprehensive support services and resources. From product demos and video tutorials to case studies and FAQs, Veeva provides a wealth of information to help organizations maximize the benefits of the Development Cloud platform. Additionally, Veeva's customer stories showcase real-world examples of how companies have achieved operational excellence and regulatory compliance with the help of Veeva's solutions. By joining the conversation in Veeva Connect, customers can engage with product leaders and peers to exchange ideas and best practices for leveraging Veeva's technology effectively.


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Empowering Emerging and Small Biotechs with Veeva Vault Safety Support Solutions

Modernize Outsourcing: Gain Operational Efficiencies, Direct Oversight, and Outsourcing Flexibility

For emerging and small biotechs looking to streamline their safety processes, Veeva Vault Safety offers a comprehensive solution that enables organizations to modernize their outsourcing practices. By leveraging Vault Safety, companies can gain operational efficiencies, maintain direct oversight of their safety data, and improve outsourcing flexibility. This allows biotechs to focus on their core competencies while ensuring compliance and efficiency in their safety operations.

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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.

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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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