Veeva SiteVault
The technology landscape is not sustainable for research sites, who are inundated with a growing number of systems to learn and use on top of their heavy workload. This is leading to industry-high levels of burnout and making it difficult to focus on patients and take on new studies.
We created SiteVault to reduce the technology and administrative burden sites face so they can focus on trial execution. Sites can manage regulatory, monitoring, eSignature, and delegation processes. It is fully compliant with 21 CFR Part 11 and includes validation, training, SOPs, and support from a team of former research professionals. SiteVault is built on the same platform used by 450+ sponsors to streamline information exchange.
Manage Multiple Sites With Ease On Veeva eISF
Sites Perspective: Challenges Working Across Sponsor Tech
Sansum Diabetes Cut Paper and Remained Compliant with SiteVault
2024 Veeva R&D and Quality Summit Site Perspective
Veeva eConsent Overview 2025
Workflow Introduction
Create and Manage eConsent Participants
PI Approval of Staff Assignments
Accept Responsibilities & Send for PI Approval
Assign Teams and Send for Acceptance
Enable Digital Delegation and Create Study Responsibilities
Assign Person Responsibilities
Digital Delegation Overview
Manage Research & Site Responsibilities
Editing an eConsent Form
Start, Review, and Sign eConsent
Reviewing Documents as a Monitor CRA
Address Monitor Feedback
Monitoring Visit Preparation
Granting Monitor/External User Access
Create and Manage Studies
Uploading Documents to the Study eBinder
Adding New Staff to SiteVault
Arizona Arthritis Cuts Costs and Expands Research with an eISF
Site eBinder
Site Documents
Veeva SiteVault eISF Demo
Uploading Source Documents
Simplify Information Sharing Between Sites and Sponsors
University of Louisville: Improving Regulatory Compliance with Veeva SiteVault