Product Overview
QVIA 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 compliant 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.
- 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
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
- Consenting workflows from the first document through amendments
- Reduce administrative burden and errors compared to paper processes
- Single sign-on and integrations to eliminate redundant data entry
- Empower site staff to focus on patient experience and answer questions
- Flexibility in document collections and version management
About the company
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 86,000 employees, IQVIA conducts operations in more than 100 countries.
