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Revolutionize Clinical Data Management with Veeva CDB

Introduction to Veeva CDB

Veeva Clinical Database (CDB) is a cutting-edge solution tailored for the medtech industry and clinical trials. In an era where clinical data managers are dealing with a myriad of data sources beyond Electronic Data Capture (EDC), Veeva CDB steps in to aggregate, clean, and transform clinical data from various origins, including third-party EDCs. This comprehensive database empowers data managers to have access to the most up-to-date data, evaluate its quality, track the progress of reviews, and log data issues seamlessly.

Key Features and Benefits

One of the core advantages of Veeva CDB is its ability to harmonize all clinical data in one centralized location. By consolidating and aligning data from EDC and other sources to a study backbone data model, this platform streamlines the data management process. Moreover, Veeva CDB eliminates the need for manual spreadsheet trackers through its intuitive data workbench, where data managers and providers can address queries within a unified system, reducing manual efforts significantly.

Efficiency and Automation

Veeva CDB revolutionizes the way clinical data is managed by introducing automation and change detection mechanisms. By automating redundant tasks and processes, this platform enables a 30-50% reduction in manual efforts, accelerating the time to lock the database. With the ability to review and clean data from multiple sources within a single system, data managers can generate data exports effortlessly, saving time and resources.

Testimonials and Success Stories

Customer testimonials, like the one from Phil Tayco, Associate Director of Clinical Data Management at Illumina, highlight the transformative impact of Veeva CDB. Through investments in electronic Trial Master File (eTMF) and Clinical Trial Management System (CTMS), organizations have been able to centralize their studies, bringing CDMS into their infrastructure effectively.

Resources and Learning Opportunities

Veeva offers a wealth of resources for those looking to delve deeper into clinical data management. From case studies like Alcon and Illumina unifying EDC to insights from the 2023 Clinical Benchmark Survey, there is a plethora of information available to support organizations in their digital transformation journey. With enterprise-wide change management techniques and success stories like Terumo's adoption of Vault eTMF and CTMS solutions, Veeva equips its customers with the knowledge and tools needed to thrive in the evolving landscape of clinical trials.

Contact Veeva CDB

For those interested in revolutionizing their clinical data management processes, Veeva CDB stands ready to provide unparalleled support. Contact Veeva Systems Inc. through their global headquarters or reach out to their sales team to explore how Veeva CDB can transform your data management strategies and accelerate your clinical trials.

Empowering Success with Veeva MedTech Training Services

Training Services for Optimal Veeva Solution Deployment

The success of implementing a Veeva solution hinges on the proficiency of the individuals utilizing, supporting, and managing the applications. Veeva MedTech Training Services offer comprehensive training and mentoring to ensure your staff possesses the expertise and skills necessary to effectively utilize, maintain, and enhance the deployed solution to align with your business needs. With tailored training programs, Veeva ensures that your team is well-equipped to optimize the functionalities of the Veeva platform.

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Revolutionizing Commercial Excellence in MedTech with Veeva MedTech

Empower Your Commercial Teams with Veeva MedTech

In today"s rapidly evolving MedTech landscape, the challenge of connecting the right content to stakeholders across various channels and interactions is more pressing than ever. Veeva"s Commercial Cloud offers a comprehensive solution to unify customer engagement, intelligence, and content management, driving commercial excellence for sales, marketing, and medical affairs teams.

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Revolutionizing Quality Management in Medtech with Veeva Vault QMS

Centralized Quality Management for Enhanced Control and Visibility

Veeva Vault QMS offers a cutting-edge solution for medtech companies seeking to revolutionize their quality management processes. This innovative software allows organizations to centralize their quality management, providing a unified global system that ensures end-to-end control and visibility for quality teams. By leveraging Vault QMS, companies can streamline quality processes and achieve better control and visibility, ultimately accelerating validation and incorporating built-in best practices.

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Unlocking Key Customer Insights with Veeva Link Key People

Understanding Key Features of Veeva Link Key People

Veeva Link Key People is a revolutionary tool that offers deep insights into important individuals in the medical field. It provides detailed profiles of scientific, digital, and clinical leaders, allowing medical teams to identify key experts, monitor their activities, and receive timely notifications. With over 4 million profiles encompassing publications, clinical trials, conferences, associations, guidelines, grants, payments, social media presence, news mentions, and impact on community practice, this product offers a comprehensive view of key players in the industry. Drawing data from more than 250,000 public sources including PubMed, conference websites, and social media feeds, Veeva Link Key People ensures that users have access to the most up-to-date and relevant information.

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Revolutionizing Global Postmarket Surveillance with Veeva Vault Product Surveillance

Simplify and Standardize Product Surveillance Globally

Veeva Vault Product Surveillance (VPS) offers a cutting-edge software solution that harmonizes global postmarket surveillance for medical devices and diagnostics. By simplifying and standardizing incident reporting management, VPS greatly enhances product safety, reliability, and quality across your organization. With a seamless integration with quality and regulatory processes, this innovative platform enables proactive complaints handling, leading to accelerated continuous innovation throughout the entire product lifecycle.

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