Welcome to Knowledge Base!

KB at your finger tips

This is one stop global knowledge base where you can learn about all the products, solutions and support features.

Categories
All

Products-Veeva Quality

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.

Comprehensive Content Lifecycle Management

One of the key features of Veeva QualityDocs is its capability to manage content throughout its entire lifecycle, from creation to disposal. This includes internal and external collaboration, enabling teams to share information securely and in a controlled manner.

Benefits of Vault QualityDocs

By utilizing Veeva QualityDocs, organizations can respond 50% faster to inspection demands, improve GxP quality and compliance, accelerate user adoption, and enable audit readiness. With detailed audit trails, automated workflows, and an intuitive user interface, Veeva QualityDocs enhances efficiency and regulatory compliance.

Customer Success Stories

Over 500 companies have successfully managed their GxP content with Veeva QualityDocs. One such example is UCB, where Veeva QualityDocs replaced four separate systems, streamlining quality content management and facilitating easy document sharing and approval processes.

Resources and Support

Veeva provides various resources for users interested in Veeva QualityDocs, including product briefs, case studies, and a reference model for modernizing GxP content management. Customers can also engage in discussions on Veeva Connect, a platform for sharing information and ideas with product leaders.

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.

Read article

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

Read article

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.

Read article

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.

Read article

Revolutionizing Clinical Trials with Veeva eCOA Solutions

Introduction to Veeva eCOA

Veeva eCOA (electronic Clinical Outcome Assessments) is a modern solution that revolutionizes the way clinical trial data is collected. It simplifies the design, management, and completion of eCOA for sponsors, sites, and patients. With 6 new standards introduced to simplify eCOA delivery and management, Veeva eCOA is at the forefront of digital transformation in the clinical research industry.

Read article