Complete Consent
Deliver eConsent to sites and study participants around the globe with confidence
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.
Products you may be interested in
Interactive Response Technology
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.
IRT eCOA
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.
Clinical Data Analytics Suite
Discover intelligent insights from streamlined data and sophisticated analytics to transform trial workflows.
Decentralized Trials
Bring trials directly to patients to improve access and engagement, increase quality and shorten timelines.
eCOA
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.