Veeva Systems announced a next-generation cloud application to streamline clinical data management and accelerate study execution. New solution eliminates the need for multiple tools with a single clinical data management application that combines coding, EDC, data cleaning, and reporting.
Headquartered in the San Francisco Bay Area (USA), with offices throughout North America, Europe, Asia, and Latin America, Veeva Systems is a leader in cloud-based software for the global life sciences industry with more than 650 customers, ranging from the world’s largest pharmaceutical companies to emerging biotechs.
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. This forces organizations to collect, clean, and analyze data across multiple systems and repositories, restricting visibility and slowing trial execution.
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.
Veeva Development Cloud is a unified suite of applications for clinical, regulatory, and quality to help organizations streamline end-to-end product development processes. Veeva has more than 220 clinical customers, 140 regulatory customers, and 180 quality customers using applications to drive greater efficiency and maintain compliance throughout the product lifecycle
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 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.