Complete Consent

The proven, global eConsent platform

IQVIA Complete Consent is the user-friendly, feature-rich electronic consent solution designed to support diverse protocols at a global scale.

Proven through more than 300 studies with over 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.

Deploy eConsent around the world with confidence

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.

Reduce protocol deviations

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 both electronic signature and print-to-sign modalities.

SEE HOW

Engaging, effective electronic informed consent

IQVIA Complete Consent supports all trial types and business models, from decentralized clinical trials to traditional site-based trials, from full-service solutions to self-managed product licensing – and every combination in between.

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