Veeva Site Solutions applications provide high-quality tools for clinical research sites to save time and manage studies more efficiently.
- SiteVault Platform: SiteVault Platform provides functionality that’s leveraged by the other SiteVault applications, for example, user and object administration.
- SiteVault eISF: A next-generation electronic Investigator Site File (eISF) providing an efficient way for investigators and site staff to manage their regulatory and source documents electronically, in accordance with ICH-GCP and industry regulations.
- SiteVault CTMS: Simplifies and collates site activities across trials enabling them to manage complex study schedules, track participant status and visit activities, monitor study payments and generate invoices all in one system.
- Veeva eConsent: Allows sites to manage and capture signatures and responses on electronic informed consent forms (eICFs).
- Sites can edit eICFs via SiteVault and the eConsent editor, as well as send and countersign completed eICFs.
- Participants receive eICFs via the MyVeeva for Patients mobile and web applications and sign electronically. The signed ICFs are stored in SiteVault.
- SiteVault users can upload paper-signed ICFs as certified copies.
For more information on Veeva Site Solutions, please see www.sites.veeva.com
Where to Start: System Overview for Site Solutions & System Overview for MyVeeva
Validation Packages: Sites & Patients Validation Packages
The following tables outline Veeva’s processes specific to Site Solutions (SiteVault) services:
SiteVault Product Processes
| Record Type | Document |
|---|---|
| Work Instruction | SiteVault PLC WI (QV-34645) |
SiteVault Services Processes
For more information on Veeva’s Services, please see Veeva Services
| Record Type | Document |
|---|---|
| Work Instruction | SV User Management WI (PS-00735) SiteVault Free Change Management WI (PS-00737) |