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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.

Proactive Complaints Handling and Continuous Improvement

One key benefit of Veeva's VPS is its seamless connection with quality and regulatory processes. This integration allows for proactive complaints handling, enabling organizations to swiftly identify and address potential product quality issues. By accelerating continuous innovation throughout the product lifecycle, VPS supports companies in delivering high-quality, safe products to consumers. The tool acts as a proactive measure to mitigate risks and enhance product reliability.

Submission Timeliness and Global Visibility

Veeva Vault Product Surveillance empowers organizations to meet submission timelines with ease. By providing an intelligent, global reportability decision tree with country-specific criteria, VPS ensures timely and accurate reporting of incidents. Real-time visibility into submissions and complaint-handling metrics offers end-to-end control, enabling informed business decisions. This level of visibility and control is crucial for maintaining product quality, enhancing patient safety, and achieving compliance standards.

Driving Growth and Quality Management

Veeva's VPS is not just a tool for compliance; it serves as a catalyst for growth and quality management in the medtech industry. Modernized quality applications like VPS act as predictors of global medtech growth, revolutionizing the way companies manage product surveillance. Through customer success stories like that of Cardinal Health, it is evident that proactive quality management, enabled by VPS, leads to improved outcomes and increased reliability in product quality.

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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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.

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Veeva Nitro: Revolutionizing Commercial Analytics in Life Sciences

Introduction to Veeva Nitro

Veeva Nitro is a groundbreaking commercial analytics platform uniquely designed for the life sciences industry. This innovative solution allows companies to harness the power of data for agile decision-making, ultimately driving commercial success.

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