Veeva Reinvents Clinical Data Management With A Single Application To Manage All Trial Data

Veeva Systems recently announced a next-generation cloud application to streamline clinical data management and accelerate study execution. Veeva Vault CDMS eliminates the need for multiple tools with a single clinical data management application that combines coding, EDC, data cleaning, and reporting. Companies can now have one application that allows them to manage study build through execution and gain a complete and concurrent view of all clinical data within a trial.

“The industry can finally move away from the complex patchwork of systems and integrations that limit the ability to leverage the range of clinical data available throughout the course of a trial,” said Henry Levy, general manager of Veeva Vault CDMS. “Veeva Vault CDMS will provide the key capabilities companies need to bring together all their clinical data so research teams can make faster, more informed decisions.”

Life sciences companies want to use a greater range of data in trials, but today’s EDC systems only manage a limited volume and diversity of clinical data.^[1] This forces organizations to collect, clean, and analyze data across multiple systems and repositories, restricting visibility and slowing trial execution.

Veeva Vault CDMS delivers on the need for a complete and concurrent view of data throughout the trial with one application for data capture, coding, cleaning, reporting, and management. Companies can now seamlessly bring data together and have daily access to all their clinical data during a trial, instead of waiting weeks or months.

Vault CDMS combines the following capabilities into a single, modern cloud solution:

• Vault Coder, available today, codes medical information with speed and accuracy in Vault CDMS. Streamline medical coding to ensure clinical teams and CROs are using up-to-date, consistent medical terms across all their studies.
• Vault EDC, also available now, maintains and manages all clinical data, including non-CRF data, in one central location. Build, manage, and run studies faster with a modern EDC and significantly improve trial execution.
• Vault Data Workbench, planned for availability in late 2019, will seamlessly bring together all trial data into a consistently formatted data lake for integrated cleaning, reporting, and export. Synchronize data automatically from Vault EDC and Vault Coder. Open APIs are available for a variety of other data sources such as ePRO, medical imaging, labs, and randomization.

Vault CDMS is part of Veeva Vault Clinical Suite, which also includes Vault CTMS, Vault eTMF, and Vault Study Startup, to unify clinical data management and clinical operations on a single cloud platform. Veeva’s suite of unified applications provides global visibility of trial processes and data for organizations to easily manage their entire trial portfolio and streamline end-to-end clinical processes.

Vault CDMS is now available with Vault EDC and Vault Coder. Expanded capability with Vault Data Workbench is planned for availability in late 2019. Learn more at veeva.com/VaultCDMS.

About Veeva Systems
Veeva Systems Inc. is a leader in cloud-based software for the global life sciences industry and other regulated manufacturers. Committed to innovation, product excellence, and customer success, Veeva has more than 650 customers, ranging from the world's largest pharmaceutical companies to emerging biotechs. Veeva is headquartered in the San Francisco Bay Area, with offices throughout North America, Europe, Asia, and Latin America. For more information, visit veeva.com.

^[1] Tufts Center for the Study of Drug Development, 2017 eClinical Landscape Study