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Enhancing Clinical Trial Efficiency with Veeva Vault eTMF

Veeva Vault eTMF: Streamlining Trial Master File Processes

Veeva Vault eTMF stands as the premier trial master file application designed to uphold the quality, timeliness, and completeness of all TMF components. With robust enterprise content management capabilities, it offers a comprehensive suite of features for uploading, version control, quality control, approval, and real-time collaboration on study documents like consent forms. This efficiency extends to supporting global outsourcing initiatives, making it easier for stakeholders to access and contribute to critical study documents.

Enhanced Compliance and Collaboration Workflows

The platform's core focus lies in managing the completeness and timeliness of TMF components through Expected Document Lists (EDLs). Leveraging the TMF Bot, content files are automatically classified, ensuring alignment with EDL requirements. Moreover, the TMF Transfer function simplifies the exchange of TMFs between sponsors and CROs, facilitating seamless communication and documentation sharing upon study closure.

Driving Efficiency and Quality in Clinical Trials

Veeva Vault eTMF introduces innovative solutions to enhance trial efficiency and maintain high-quality standards throughout the trial process. By improving data quality, reducing duplicates and discrepancies, the platform streamlines registration management processes. Furthermore, it offers global visibility into the marketing status of products, accelerates health authority responses, manages queries, and commitments efficiently, ensuring compliance and enhancing trial outcomes.

Testimonials and Success Stories

Phil Tayco, Associate Director of Clinical Data Management at Illumina, commends Veeva's solutions, sharing his success story in bringing all studies in-house through investments in eTMF and CTMS. This testimonial showcases the tangible benefits and efficiencies that organizations experience when leveraging Veeva Vault eTMF for their clinical trials.

Resources and Further Learning Opportunities

Explore a wealth of resources offered by Veeva MedTech to deepen your understanding of clinical trial management. Discover case studies, articles, videos, and surveys that shed light on best practices, industry insights, and success stories. Whether you're interested in eTMF, CTMS, or payments integration, Veeva provides comprehensive materials to support your journey towards optimized clinical trial operations.

Revolutionizing Medical Affairs with Veeva MedTech

Enhancing Scientific Exchange and Building Relationships

Veeva MedTech offers a comprehensive solution through the Veeva Medical Suite, designed to elevate scientific exchange and foster long-term relationships between medical affairs professionals and healthcare providers (HCPs). By leveraging this suite, medical affairs teams can collaborate effectively with HCPs to enhance patient outcomes. This integrated solution brings together key customer engagement processes and scientific procedures, empowering medical affairs to revolutionize organizational strategies.

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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.

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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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