About
The proven, global electronic informed consent platform
IQVIA Complete Consent is the user-friendly, feature-rich eConsent solution designed to support diverse protocols at a global scale.
Proven through >300 studies with >400,000 participants and 10,000 sites, we offer complete flexibility to meet your trial needs while delivering more convenience for sites and a better experience for patients.
IQVIA Complete Consent provides an easy, secure way to deliver highly engaging, regulatory compliant electronic consent for trials of all types so you can optimize enrollment and engagement, while realizing efficiencies to achieve better outcomes across the entire study lifecycle.
Connect with an IQVIA expert today to explore how Complete Consent can support your unique protocol, site and participant needs.
This product is intended for
- Clinical Operations Specialist
- Clinical Trial Project Manager
- Clinical Trial Lead
- Clinical Research Project Manager
- Director Clinical Research
- Vice President Clinical Research
- Director of Patient Services
- Director Life Science
- Clinical Research Associate
- Clinical Research