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Enhancing Safety for Emerging and Small Biotechs with Veeva Quality

Introduction to Veeva Quality Solution

Veeva Quality offers a comprehensive solution tailor-made for emerging and small biotechs looking to enhance their safety operations. With Veeva Quality, these organizations can gain significant operational efficiencies, increased oversight, and the flexibility to outsource when needed. The platform provides a modernized approach to outsourcing, allowing users to oversee and control their data effectively, ensuring compliance and streamlined decision-making processes.

Preparation for Growth and Scalability

One of the key features of Veeva Quality is its ability to help organizations prepare for growth by establishing a strong foundation for scalability. By leveraging this solution, biotechs can validate safety solutions within weeks, as experienced by many satisfied customers. This rapid validation process is crucial for organizations looking to expand and handle increased data volumes efficiently and securely.

Automation and Operational Efficiency

Veeva Quality enables users to do more with less through automation and operational efficiency tools. By integrating safety processes into a unified platform, organizations can reduce clinical trial costs significantly. This integration streamlines case processing, reporting, and submissions, leading to cost savings without compromising on quality or compliance. The platform also simplifies safety processes, making case processing and pharmacovigilance document management easier and more efficient.

Customer Testimonials and Success Stories

Veeva Quality has garnered praise from customers for its intuitive interface, ease of use, and the invaluable access it provides to safety data. Testimonials from industry leaders like Hanssar Chacon, Senior Director of Global PV and Risk Management at CRISPR Therapeutics, highlight the platform's superiority over competitors. Customers have successfully modernized their outsourcing practices, gained direct oversight and control of their data, and established a scalable foundation for growth with Veeva Quality.

Transforming Pharmacovigilance with Vault Safety

Biotechs, biopharma companies, and CROs are leveraging Veeva Quality to transform their pharmacovigilance operations. Vault Safety has become a game-changer in the industry, offering cloud-based software that caters to the unique needs of the global life sciences sector. By joining the conversation in Veeva Connect, industry professionals can exchange information, share ideas, and stay abreast of the latest developments in safety and quality management.

Empowering Commercial Execution with Veeva Quality Services

Maximize Engagement and Impact

Veeva Quality Services, part of the Veeva Commercial Cloud, serves as the technology foundation for companies looking to enhance their commercial execution. By leveraging this solution, sales, service, marketing, and medical teams can collaborate seamlessly, leading to more customer-centric and coordinated engagement. This connected software and data solution, in conjunction with Veeva Data Cloud, accelerates insights, innovation, and efficiency.

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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.

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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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