Better Inform your Patients
with Veeva eConsent

Deliver a better site and patient experience through
an end-to-end informed consent process.


Connect and network with R&D and Quality leaders.
Register now

Veeva eConsent

Veeva eConsent simplifies the set-up, completion, and review of consent, reducing administrative burden and ensuring compliance for sites and study teams.

This enables study teams to make patient participation in clinical trials easier through a user-friendly application to access key information and complete consent electronically.

Benefits

Better Patient Experience

Give patients direct and convenient access to their study documents on their own device via the MyVeeva for Patients app.

Reduce Site Burden

Remove administrative burden by using one eConsent system across all studies without the need for additional systems or applications.

Faster Study Execution

Accelerate informed consent form (ICF) creation and review by eliminating burdensome manual processes.

Stronger Compliance

Stay informed with complete visibility into consent status, streamlining consent monitoring and ensuring study compliance.

Features

End-to-end eConsent Platform

Unified system seamlessly connecting sponsors, sites, and patients across the entire consent process.

Flexible Consent Options

Enable in-person or remote eConsent on any device. A signed copy of the ICF is stored in the patient's app and can be downloaded anytime.

Reduced Authoring and Review Cycles

Creation and reuse of consent templates through easy-to-use editor tools, streamlining authoring, review, and approval of consent documents.

Sharing and Collaboration

Easily share and collaborate on informed consent forms between sponsors, sites, and IRBs.

Version and Audit Controls

Automate versioning and view date / time stamps for better compliance and traceability. Easily compare documents to previous versions to see what has changed.

Familiar Site Interface

Site friendly solution to manage eConsent, reducing administrative burden and training requirements.

Intuitive Patient Interface

Guide patients with an easy-to-navigate layout and ensure all sections are reviewed prior to sign off.

Interactive Content

Easily add images and videos to aid in comprehension. Add custom questions to collect additional information and enhance the consenting process.

Reporting

Full visibility of patient consent status, date, and version gives sponsor, monitor, and site staff the vital information needed to support compliance.

Validated and Secure Cloud Platform

Veeva eConsent is fully validated by Veeva and supports compliance with HIPAA and regional data privacy requirements.

Resources

Shifting from Paper to Digital Patient Consent
Article Shifting from Paper to Digital Patient Consent
Read the Veeva eConsent Product Brief
Product Brief Read the Veeva eConsent Product Brief
Delivering an eConsent Solution to Support Patients, Sites, and Study Teams
Blog Delivering an eConsent Solution to Support Patients, Sites, and Study Teams
First Patient Completes Digital Consent with Veeva Clinical Network
Press Release First Patient Completes Digital Consent with Veeva Clinical Network