IQVIA’s Patient Suite lets you simplify today’s complex clinical landscape with solutions that integrate technology, data, and delivery around the world.
IQVIA Patient Suite blends the innovative platforms and expert services of Complete Consent, IRT, eCOA, and Connected Devices. These solutions harmonize high-quality, compliant data while optimizing trial workflows through automation.
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.
IQVIA IRT is a randomization and trial supply management solution that supports today’s sophisticated protocols and ensures the right patient gets the right treatment at the right time.
In addition to the scalable platform, our experts initiate planning, build standard workflows, and ensure data integrity for site-based and decentralized trials.
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.
As trial sponsors face increasing pressure to deliver new treatments to market faster, connected digital medical devices play a more vital role. IQVIA Connected Devices accelerate trial outcomes by streamlining the selection and deployment of medical devices to collect and analyze data.
Multiple stakeholders saved time and effort by integrating IQVIA eCOA, Complete Consent, and IRT.
in effort during user acceptance testing for the clinical team
in sponsor effort during site/user creation through a single source of data across integrated IRT and eCOA solutions
in sponsor effort during site/user creation through a single source of data across integrated IRT and eCOA solutions
in effort for clinical teams during the start-up phase of the trial
How IQVIA delivers a holistic view of lung disease by combining patient-reported outcomes and objective data
Interactions between patient organizations and life sciences companies
Part 2: How eConsent delivers value for sponsors
Interoperable technology that improves data quality and usability while optimizing trial conduct
A tailored solution gave a global oncology program the head start it needed
Don’t let vague consent forms prevent you from (re)using valuable specimens
How to deliver highly engaging informed consent for better study outcomes
Specialized expertise and customized solutions across 14 therapeutic centers of excellence, including oncology, GI/NASH, pediatrics, neurology and rare diseases.
Improve the performance of your clinical trials with the power of the IQVIA CORE.
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