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Products-Veeva MedTech

Efficient and Compliant Content Management with Vault PromoMats

Streamlined Content Management for the MedTech Industry

Vault PromoMats by Veeva MedTech is a cutting-edge regulated content management application designed to support the complete lifecycle of promotional content. With PromoMats, organizations can ensure compliant content creation, efficient review and approval processes, seamless digital asset management (DAM), claims management, and modular content development. One of the key features of PromoMats is the Brand Portal, a centralized repository that serves as a single source of truth, making content easily accessible and reusable for all team members.

Cloud-Based Collaboration and Accessibility

Delivered in the cloud, PromoMats allows instant access to all teams, simplifying collaboration and enabling global asset sharing. This cloud-based approach ensures greater brand alignment while helping organizations control costs efficiently. Additionally, being cloud-based means that teams can collaborate in real-time, eliminating delays and enhancing productivity.

Key Benefits of Vault PromoMats

Vault PromoMats offers several key benefits to organizations in the MedTech industry. Firstly, it accelerates the speed at which compliant content can be produced at scale, facilitating faster time-to-market for promotional materials. Secondly, the integrated features for review and approval, claims management, and digital asset management streamline processes, reducing the time it takes to get content live. Moreover, PromoMats ensures cross-channel compliance by addressing global regulatory requirements through robust claims management, version control, and detailed audit trails.

Enhancing Collaboration and Productivity

Another significant advantage of PromoMats is its scalability and built-in digital asset management capabilities. The platform offers fully configurable workflows and a robust feature set tailored for the MedTech industry. Standard version control and a dynamic security model ensure that all team members work on the most up-to-date content, promoting global collaboration and maximizing productivity. With PromoMats, organizations can transform their content lifecycle, achieving faster review times, expedited claims substantiation, and complete traceability of all assets.

Customer Success Stories and Resources

Veeva's Vault PromoMats has garnered praise from customers across the MedTech industry for its effectiveness in managing commercial content. Case studies and customer stories exemplify how organizations such as BD, Roche Diagnostics, and Coloplast have streamlined their operations and achieved excellence in marketing with the help of PromoMats. Apart from success stories, Veeva offers various resources such as feature briefs, explainer videos, articles, and infographics to help organizations understand and leverage the full potential of PromoMats.

Empowering Global Regulatory Compliance with Veeva MedTech's Vault RIM Platform

Streamlined Regulatory Compliance and Information Management

In today's rapidly evolving regulatory landscape, global medical device and diagnostics manufacturers face challenges related to globalization, supply chain complexity, patient safety, and new regulations. These factors can significantly impact the total product lifecycle and lead to manual, cumbersome processes that slow down time to market. Veeva MedTech's Vault RIM Platform offers a comprehensive solution to streamline global regulatory compliance and information management. By unifying systems and providing a single source of truth for registrations management, submissions, publishing, and archival, this platform enables organizations to ensure compliance and accelerate speed to market.

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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.

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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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