E-Technologies STREAM

  1. Fast, Flexible, And Proven Direct-From-Patient Data Capture With eCOA 5/3/2022

    Delve into how IQVIA eCOA captures patient data in a way that always keeps patients top of mind.

  2. Align eDiary Design With Assessment Schedules 4/2/2025

    Ensure alignment with your study protocol by leveraging the Sculptor portal to simulate eDiary completion and top-down scheduling, allowing for real-time preview and modifications.

  3. Eliminating Friction Across RTSM With Elosity 5/20/2026

    This session cuts into where operational complexities actually surface after go‑live and shows how Elosity eliminates it through controlled change, real‑time insight, and scalable oversight across the full trial lifecycle.

  4. Document Processing: A New Hope 8/8/2024

    Tired of slow, error-prone document processing? Discover how top companies are boosting speed and accuracy while slashing costly rework. Watch now to learn how you can achieve TMF excellence faster.

  5. Introducing eCOA+ Streamlined Evidence Generation 1/16/2024

    Watch as Colin Weller, Vice President and General Manager of the Digital Outcomes and Evidence Platform at Medable, Inc., articulates the vision for eCOA+ and the trajectory of evidence generation.

  6. Central eSource: Leveraging Site Technology 2/27/2025

    In this presentation, CRIO founder and co-CEO Raymond Nomizu delves into how sponsors can leverage the electronic source trend among sites through the use of Central eSource.

  7. 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.

  8. Veeva eCOA Demo 6/24/2024

    See firsthand how this modern build platform, which includes a ‘one-click’ library of pre-validated questionnaires, reduces build times by 75% and means mid-study updates can be actioned in minutes.

  9. IQVIA eCOA: Amplifying The Patient's Voice 4/19/2024

    Dive deep into the capabilities of IQVIA's eCOA with our expert Edward Bartels. He will focus on how to effortlessly create a diary, schedule site/participant assessments, and intuitively manage translations and compliance.

  10. Closing The "Compliance Gap" In TMF Archiving 8/15/2022

    Discover how organizations are crossing this “compliance gap” with PhlexTMF for Viewing, an easily accessible TMF archive for internal use, audits, and inspections.