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Fremont, CA: Veeva Systems recently unveiled the new Veeva Digital Trials Platform, allowing clinical trials to run smoothly and data to move freely across stakeholders. The platform is already accessible to early adopters, provides an entire and linked technological ecosystem that includes research locations, patients, and trial sponsors. Additionally, vault Clinical Suite, clinical operations, and clinical data management platform for sponsors and enhanced CROs to add Site Connect and eConsent.
The following main solutions are part of the full product offering:
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The patient consent procedure exemplifies how the Veeva Digital Trials Platform facilitates cooperation and data flow. Sponsors create and approve a consent form using Veeva eConsent, which automatically flows to sites using Veeva SiteVault Free. The permission form may then be modified, IRB approval obtained, and patients consented to use the MyVeeva mobile application. In addition, the patient status and permission form are instantly available in Vault Clinical Suite as verified and reportable data for the sponsor.
The Veeva Digital Trials Platform will enable faster, more efficient trials with better data quality and patient diversity by answering the life sciences industry's requirement for a total, standardized, linked solution.
“By bringing together the growing community of research sites using Veeva SiteVault Free with sponsors using Vault Clinical Suite, we aim to accelerate the move to digital trial execution,” said Jim Reilly, vice president, Vault R&D at Veeva. “The Veeva Digital Trials Platform will make clinical trials easier and faster for patients, sites, and sponsors.”
Vault Clinical Suite improves clinical operations and clinical data management by providing the most comprehensive suite of clinical solutions on a single cloud platform, including EDC, coding, data management, study start-up, eTMF, CTMS, and payments. As a result, life sciences firms can boost their visibility, streamline their end-to-end procedures, and enhance how sponsors, CROs, and sites collaborate across the clinic.
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