Veeva Digital Trials Platform
The Veeva Digital Trials Platform is a new solution to significantly advance clinical trial execution by providing a complete and connected technology ecosystem that spans patients, research sites, and trial sponsors.
With seamless process execution and flow of data across all stakeholders, the Veeva Digital Trials Platform will deliver faster, more efficient trials that achieve higher data accuracy and increased patient diversity.
The comprehensive product offering delivers solutions built for the unique needs of patients, sites, and sponsors:
Sites
SiteVaultA free application for sites to modernize their operations and run connected clinical trials with sponsors using Vault Clinical Suite
Sponsors
Vault Clinical SuiteClinical operations and clinical data management for sponsors and CROs
Patients
MyVeeva for PatientsA single, intuitive application that makes it easy for patients to participate in clinical research
The patient consent process illustrates how the Veeva Digital Trials Platform drives collaboration and data flow.
Sponsors
Sponsors use Veeva eConsent to author and approve a consent form, which flows automatically to sites using Veeva SiteVault Free.
Sites
Sites can modify the consent form, obtain IRB approval, and consent patients with the MyVeeva mobile application.
Patients
Patients access study documents on their own devices and can quickly complete the consent process, which is immediately available as validated and reportable data for the sponsor.
LEO Pharma Accelerates Move to Digital, Patient-centric Trials
Reduction
in clinical trial costs
Reduction
in clinical trial time
Higher
clinical data accuracy
Increased
patient diversity and improved patient experience
Resources
If you would like more information please contact us.
Contact Us