Complete Consent
IQVIA Complete Consent is the user-friendly, flexible, and feature-rich electronic informed consent solution built to support diverse protocols at a global scale.
Deliver highly engaging, regulatory compliant electronic eConsent
Verified through more than 350 studies with over 400,000 participants and 10,000 sites, IQVIA Complete Consent meets the needs of all trial types.
eConsent helps sponsors achieve better outcomes across the entire study lifecycle, while delivering an enhanced experience for patients and more convenience for sites.
DEPLOY COMPLETE CONSENT AROUND THE WORLD WITH CONFIDENCE
IQVIA Complete Consent
IQVIA Complete Consent delivers unmatched value to all stakeholders
Sponsors
- Compliant data by reducing consent-related protocol deviations
- Global delivery with configurable documents and multiple language support
- Increase patient recruitment and retention to accelerate trial conduct
- Deep experience in oncology, vaccines, cardiovascular, and more therapeutic areas
- Consent reporting and analytics for study design and enrollment strategies
Sites
- Consenting workflows from the first document through amendments
- Reduce administrative burden and errors compared to paper processes
- Single …
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