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Transforming Clinical Trials with VEEVA VAULT CTMS

End-to-End Trial Management

VEEVA VAULT CTMS is a comprehensive enterprise trial management system that offers a complete solution for managing and monitoring both in-house and outsourced trials. It allows for proactive management of trials and facilitates a more connected and efficient digital future in the clinical research space.

Key Features and Capabilities

The system comes equipped with dashboards and reports that enable tracking of essential trial indicators such as enrollment and milestones. These dashboards provide a detailed view of the trial progress and allow for immediate action to be taken. Additionally, monitoring visit reports are automated within the system, with dynamic question branching to support efficient data collection and management. Trip reports are seamlessly filed within the Vault eTMF, ensuring all documents are consolidated and organized for easy access.

Integration and Connectivity

One of the distinctive features of VEEVA VAULT CTMS is its seamless integration with VEEVA VAULT EDC. This integration streamlines processes related to enrollment, monitoring, payments, and navigation to casebooks directly from within the CTMS. Furthermore, investigator interactions are synchronized with Veeva CRM, offering a comprehensive 360-degree view of all trial-related activities.

Benefits and Efficiency

By utilizing VEEVA VAULT CTMS, research teams can experience faster and higher-quality trials. The system enhances productivity by providing role-based dashboards and intuitive navigation, allowing study teams to work more efficiently. Decision-making is improved with real-time insights into trial status, enabling closed-loop issue management and strategic planning. Moreover, the proactive risk management capabilities of the system help identify and mitigate risks, ultimately speeding up trial execution.

Customer Testimonials and Success Stories

With over 100 customers, including leading companies like Illumina, VEEVA VAULT CTMS has proven to be a mature and trusted solution for clinical trial management. Customers have reported significant reductions in monitoring planning and execution time, improved efficiency in issue management, and substantial time savings per trip report. Testimonials from industry professionals highlight the positive impact of integrating eTMF and CTMS to streamline trial operations and bring studies in-house.

Learn More and Get Started

Explore the resources available on the Veeva MedTech website to learn more about VEEVA VAULT CTMS. From articles and videos to benchmark surveys and change management techniques, there is a wealth of information to help you understand the capabilities and benefits of this innovative trial management system. Contact the Veeva team to discover how VEEVA VAULT CTMS can transform your clinical trials and support your research endeavors.

Revolutionize Clinical Research with Veeva MedTech's Comprehensive Clinical Platform

Streamlining Clinical Study Processes

In today's landscape of clinical research, the demand for real-world evidence and data, coupled with stringent global regulatory requirements, has significantly increased the complexity of conducting clinical trials. This has resulted in extended product development cycles, slowing down the process of bringing medical devices and diagnostics to market. Veeva MedTech's Clinical Platform addresses these challenges by providing a solution that streamlines clinical study processes and enhances clinical data management. By centralizing all clinical activities within a single platform, including study documents, sponsors, site payments, and more, the Veeva Clinical Platform offers a standardized approach to managing the entire clinical research process.

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Revolutionizing Clinical Outcome Assessments with Veeva eCOA

Introduction to Veeva eCOA

Veeva eCOA (Electronic Clinical Outcome Assessment) is a cutting-edge solution designed to facilitate the seamless capturing of questionnaire responses directly from patients. This innovative approach ensures the consistent and real-time tracking of success criteria, ultimately transforming the way clinical trials are conducted.

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Empowering Clinical Data Management with VEEVA CDB

Revolutionizing Clinical Data Management

In the realm of clinical data management, the need to aggregate, clean, and transform data from various sources is paramount. Veeva Clinical Database (CDB) emerges as a pioneering solution tailored for the medtech industry and clinical trials. Unlike traditional data management systems, Veeva CDB streamlines the process by consolidating data from diverse sources such as EDC, laboratories, and ePRO systems. With seamless integration and data harmonization, CDB ensures that data managers have access to the latest information while tracking review progress and resolving data issues effectively.

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Unlocking Efficiency and Agility with VEEVA VAULT EDC

Streamlined Data Collection and Management

VEEVA VAULT Electronic Data Capture (EDC) is a powerful solution designed to address the intricacies of modern clinical trials. With over 100 satisfied customers trusting its capabilities, Vault EDC offers a comprehensive platform for collecting, reviewing, and processing trial data efficiently. From designing patient forms during study initiation to locking data at the conclusion of the study, Vault EDC simplifies the entire data management process.

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Revolutionizing Medical Affairs with Veeva Medical Suite

Empowering Scientific Engagement

Veeva Medical Suite offers Vault CRM for MedTech, a comprehensive tool that empowers medical affairs to drive scientific engagement. With this solution, organizations can effectively share content, capture crucial medical insights, and foster meaningful interactions with healthcare professionals (HCPs) and key opinion leaders (KOLs). By leveraging Vault CRM for MedTech, medical affairs teams can build long-term relationships, ultimately enhancing patient outcomes.

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