PATIENT ENGAGEMENT SUITE

Simplify the trial experience

IQVIA Patient Engagement Suite products enhance participant experience, deliver better data quality and insights, and improve clinical trial outcomes.

E-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.

It 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.

IRT SOLUTIONS

Accomplish more with a flexible, proven IRT

The IQVIA IRT Solution: Comprehensive randomization and trial supply management solution continues to be trusted by trial partners across study phase, complexity, and therapeutic area.

Built on a robust, scalable platform, our patient-centric approach to technology delivery provides exceptional value and peace of mind for sponsors and their patients in clinical trials.

ELECTRONIC CLINICAL OUTCOME ASSESSMENT

An eCOA solution built for you, designed for your patients

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.

Accelerate trial start up by up to 75% with the industry’s largest digital assessment library.

CONNECTED DEVICES

Power clinical trials with better data

As trial sponsors face increasing pressure to deliver new treatments to market faster, connected digital medical devices play a more critical role. IQVIA Connected Devices accelerates trial outcomes by streamlining the selection and deployment of medical devices to collect and analyze data.

IRT + eCOA BUNDLE

Optimize your trial with best-in-class product integrations

Combine IQVIA’s IRT and eCOA solutions together to improve study quality, accelerate decision making, and reduce site and sponsor burden. Plus you can add the IQVIA Complete Consent option to support patient enrollment and study efficiency.

Seamlessly integrate best of breed, modular, interoperable technologies proven to optimize efficiency and enhance trial outcomes.

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