Product Overview
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.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
Veeva eConstent reduces errors related to signature dates and times, easily track consent versions, and automatically generate screening logs.
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.
Sharing and Collaboration: Easily share and collaborate on informed consent forms between sponsors and sites.
About the company
Our vision is to build the industry cloud for MedTech. More than just software. We are committed to helping the entire industry modernize to speed the total product lifecycle, bringing products to patients faster. We do this by partnering with the industry and MedTech companies to address the unique challenges we face.
