Patient Engagement Suite

  1. How eConsent Delivers Value For Sponsors 9/21/2023

    Delve into the data substantiating experiences with electronic informed consent to better understand their positive impact on the outcomes of clinical trials.

  2. Data-Driven Adaptive Trials Enhance Safety, Progress, & Economics 7/21/2023

    By offering guidance on optimizing ROI from extensive data collections and various endpoints in clinical studies, learn how IRT technology can enhance the data-driven approach for sponsors.

  3. IQVIA Integrated Complete Consent IRT eCOA 7/14/2023

    Learn how to improve data quality and usability while optimizing trial conduct with this interoperable technology.

  4. Drug Accountability And Returns Management 6/8/2023

    See how sponsors are using electronic solutions for Drug Accountability (DA) and experiencing significant increases in efficiency and accuracy that these methods provide.

  5. Successful Subject Creation With eCOA, eConsent, & IRT Process Flow 5/26/2023

    Watch this process video to see how IQVIA’s integrated Interactive Response Technology (IRT) and electronic Clinical Outcome Assessment (eCOA) solution combined with unified platform delivery drives study orchestration and optimization.

  6. Reducing Macroeconomic Pressures On Clinical Trial Supply: Session 2 4/28/2023

    Join IRT industry veteran and drug supply expert Stefan Dürr for a discussion about how to reduce the impact of both traditional and emerging macroeconomic pressures on clinical trial supply.

  7. Cenduit Interactive Response Technology 4/25/2023

    Accelerate study start-up and amendments, simplify site and sponsor experience, reduce trial supply costs and improve study decision making while ensuring quality standards and patient safety during your trial with Cenduit Interactive Response Technology.

  8. Beyond Integration: Flexible Orchestration Of IRT And eCOA Solutions 4/25/2023

    Consider how the orchestration of integrated response technologies for randomization and trial supply management, and electronic clinical outcomes assessments can improve configurability, rapid study start-up, and flexible mid-study changes.

  9. IQVIA’s Integrated IRT eCOA Platform 4/25/2023

    Improve study quality, accelerate decision making, and reduce site and sponsor burden by using IQVIA’s integrated Interactive Response Technology and electronic Clinical Outcome Assessment solution.

  10. Streamlining Clinical Trials: A Guide To Migrating From Paper To EDC 4/19/2023

    Electronic modes have been shown to improve data quality in clinical trials compared to collecting patient-reported outcomes in a paper format. Address how equivalency can be achieved when migrating PROs from paper to ePRO.