Complete Consent
The proven, global eConsent platform
IQVIA Complete Consent is the user-friendly, flexible, and feature-rich electronic informed consent solution built to support diverse protocols at a global scale.
IQVIA Complete Consent is the user-friendly, flexible, and feature-rich electronic informed consent solution built to support diverse protocols at a global scale.
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.
In a review of nearly 100 trials across IQVIA that used eConsent, compared to paper, consent-related major and critical protocol deviations were reduced from an average of 14% to only 6%. This entailed a combination of electronic signature and print-to-sign modalities.
The right remote consent solution provides participants with tools to understand the study and pose questions to site personnel, while minimizing disruptions to their daily lives. An eConsent solution should also empower study teams and sites to spend more time conducting the study by reducing the burden of administrative tasks such as addressing deviations.
IQVIA Complete Consent supports all trial types and business models, from decentralized to traditional site-based trials, from standalone self-managed to full-service solutions with implementation services. We partner with sponsors at every step so you can deliver eConsent at sites around the world with confidence.
Discover how IQVIA Complete Consent delivers an accessible solution to patients, operational efficiencies to sites, and a powerful platform to sponsors implementing eConsent flexibly and compliantly around the world.
Fast, flexible and proven, IQVIA’s industry-leading electronic clinical outcome assessment (eCOA) platform ramps up efficiencies, delivers real-time data, and sharpens insights through best-in-class technology and a better patient experience.
Power your decentralized trial with an agile randomization and trial supply management solution that supports supply flexibility and optimization as well as adaptable direct to patient options.
Improve study quality, accelerate decision making and reduce site and sponsor burden by harnessing the power of IQVIA’s integrated Interactive Response Technology (IRT) and electronic Clinical Outcome Assessment (eCOA) solution.