Deliver a Better Patient Experience
Make participation in clinical trials easier with Veeva eConsent.
Make participation in clinical trials easier with Veeva eConsent.
Veeva eConsent provides a digital way to consent clinical trial participants in-person or remotely.
Break free from legacy tools and cumbersome paper documents. Give your patients access to a modern digital consent experience that fits into their daily lives. Use eConsent across all your studies to drive efficiency, quality, and provide a better patient experience.
Veeva eConsent is fully validated by Veeva and supports compliance with HIPAA, 21 CFR Part 11, and regional data privacy requirements.
Better Patient Experience
Eliminate the need for patients to carry around paper and provide convenient access to study documents and site information on their own device.
Reduce Staff Burden
Eliminate printing and copying, simplify screening, and easily access documents with a single system that can be used across all studies and works seamlessly with SiteVault.
Stronger Compliance
Reduce errors related to signature dates and times, easily track consent versions, and automatically generate screening logs.
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.
Patients and study staff sign ICFs in full compliance with 21 CFR Part 11.
Full visibility of patient consent status, date, and version gives sites and monitors the vital information needed to support compliance.
Automate versioning and view date/time stamps for better compliance and traceability. Easily compare documents to previous versions to see what has changed.
Guide patients with an easy-to-navigate layout and ensure all sections are reviewed prior to sign-off.
Easily share and collaborate on informed consent forms between sponsors and sites.
Modify ICFs with easy-to-use editor tools to standardize consent forms across your studies. *Paid add-on.
Easily add images and videos to aid in comprehension. Add custom questions to collect additional information and enhance the consenting process. *Paid add-on.
Manage eConsent across all studies through SiteVault, reducing administrative burden and training requirements.
Veeva eConsent is fully validated by Veeva and supports compliance with HIPAA and regional data privacy requirements.
The continuity of having information at your fingertips and being able to answer questions instantly is invaluable.
Staci McDonald
Vice President Global Scientific Clinical Operations, Celerion
Read Customer Story
“Veeva eConsent makes the process easy for our patients and allows us to break down the barriers of paper and location, expanding the reach of our study.”
Charles Sydnor
Project Manager, Croofoot Research Center
Read MoreVeeva eConsent may be provided by your sponsor for a study or enabled within your SiteVault account to use across all studies. Contact us to learn more.
Yes. While you must have a SiteVault account, you can choose to only use the eConsent functionality within SiteVault on all studies or only specific studies.
Yes, creation of eConsent for use across all your studies is available as a paid add-on. Veeva eConsent is not a sponsor-specific platform, which allows you to standardize your SOPs, workflows, and training for consenting across all studies to improve compliance and efficiency. Learn more about the benefits of a standard eConsent solution here.
Contact us to learn how to get access to Veeva eConsent.
Contact Us
