IRT RESOURCES
Extend your understanding of IQVIA IRT here
Explore our library of IRT resources including thought leadership papers, on-demand webinars, case studies, and other valuable content.
Explore our library of IRT resources including thought leadership papers, on-demand webinars, case studies, and other valuable content.
Explore how seeking an IRT specialist can improve planning, increase integration with other clinical systems, and mitigate study risks.
Integrated clinical trial platforms enhance data quality, facilitate cooperation across trial functions, and boost trial efficiency.
IQVIA experts discuss advancements in drug accountability delivered through IRT, which include managing site variances and ensuring a lean, sustainable supply chain.
Learn how SAVE reduces clinical team effort and reduces shipping and IP costs during studies.
Embracing IRT optimizes clinical trial operations, enhancing patient satisfaction, researcher efficiency, and sponsor results.
IQVIA’s approach to technology delivery provides exceptional value for sponsors and their patients in clinical trials.
Optimize technology to support faster, safer, and more reliable drug development.
IQVIA IRT improves quality and efficiencies in medical device trials.
Enhance technology to ensure safety and accountability while minimizing costs and risks.
Learn how this solution automates tasks, resolves redundant data entry, and enhances study communication for sites and sponsors.
Explore insights from IQVIA IRT experts in clinical operations, therapeutic areas, and data management
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.
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.
Deliver eConsent to sites and study participants around the globe with confidence