Patient Engagement Suite

  1. eCOA Licensing Guide 3/7/2024

    In this comprehensive guide, IQVIA's eCOA library and licensing specialists, Kayla Doyle and Piero Bindi, explore five essential steps for obtaining licenses for the assessments required in your clinical trial.

  2. Medical Device Trial Integration 3/7/2024

    Each device, with its unique technology and study parameters, presents a distinctive challenge that demands precision at every turn. Learn how we can help to revolutionize your medical device trial journey.

  3. Right-Size Your eConsent Approach 11/17/2023

    Delve into the art of tailoring the eConsent experience to match the specific needs of your study and patients, such as how to craft patient-centric eConsent documents, select appropriate delivery models, and more.

  4. Innovations In IRT 11/2/2023

    Review the latest innovative techniques employed by IQVIA IRT, including innovations in the design, delivery, conduct and monitoring of clinical trials.

  5. 3 IRT Tactics Being Used To Streamline Supply Logistics 10/26/2023

    Shipping and storing leading-edge therapeutics require complex logistics, but enhanced automation and process simplification ensure that sites and patients have the drugs they need when they need them.

  6. The Key To Compliance, Patient Safety, And Risk Based Monitoring 10/24/2023

    eClinical technologies are becoming more commonplace in drug development. Uncover how digital solutions are helping sponsors improve efficiency and accuracy within their clinical trials.

  7. Supply Chain Logistics Experts Share Best Practices 10/13/2023

    Access the transcript from a recent Clinical Leader Live webinar where supply chain optimization experts shared best practices for streamlining shipments, reducing waste, and enhancing accountability.

  8. Level Up Your Supply Chain Initiatives 10/10/2023

    Shipping and storing advanced therapeutics are complex processes, but advancements in accountability, wearables, and technology capture real-time factors critical to safety and protocol.

  9. 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.

  10. Data-Driven Adaptive Trials Enhance Safety, Progress, And 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.