IQVIA Complete Consent transforms the traditional paper-based informed consent process into a secure, patient-centric digital experience that improves enrollment, patient understanding, and regulatory compliance across global clinical trials. Supporting multimedia content, real-time review tools, configurable workflows, and digital consent on virtually any device, the platform accommodates studies ranging from simple observational research to complex oncology and CNS trials. Available in more than 65 countries, it integrates with the IQVIA Patient Suite to streamline onboarding, reduce consent errors, and improve operational efficiency. Across nearly 100 clinical trials, the solution reduced consent-related protocol deviations from 14% to 6%, while 100% of participants found it easy to use

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