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. TMF Completeness: Simple Solutions For A Complex Problem 9/7/2021

    In this session, two of the top technology minds in TMF management will demonstrate and a simple yet innovative way to measure completeness at any point during the trial. 

  3. Is It Worth The Effort To Switch To Veeva's EDC? 8/14/2024

    Kronos Bio discusses how their oncology biotech switched to Vault EDC for faster, more flexible builds.

  4. Harness The Power Of eCOA In Your Next Trial

    In this webinar, explore the importance of eCOAs, how they have evolved from the standard paper diaries, and what efficiencies you can realize from them.

  5. Rethinking Today's ePRO Delivery For Tomorrow's Clinical Trials 6/24/2024

    Willie Muehlhausen, Co-CEO and Founder of Safira Clinical Research, and Tim Davis, VP of Strategy at MyVeeva for Patients, discuss how ePRO delivery needs to change to better serve modern trials.

  6. Study Build And Scheduler Tools 3/27/2025

    Empower your study participants with IQVIA eCOA’s tailored user experiences, flexible event triggers for clinicians, comprehensive training resources, and 24/7 support for seamless study management.

  7. Keeping Up With ClinOps: Why And How To Improve Delivery 11/6/2023

    Industry experts discuss the concept of a trial platform as a service and how it can accelerate and enhance the day-to-day functions of clinical operations throughout the entire lifecycle of a study.

  8. Streamlining Translations For Global Studies 3/27/2025

    Ensure seamless, accurate global study translations and efficient localization with IQVIA eCOA, leveraging our proven vendor relationships and streamlined process to keep your study on track.

  9. Crossing The TMF Compliance Gap With Inspection-Ready Access For Closed Studies 4/30/2021

    Your drug study is closed, you need inspection-ready access to the Trial Master File, but your CRO is ready to get the TMF out of their system and wants to send you a zip folder full of documents. What do you do? In this session, we explore an innovative new way to ensure your TMF stays secure while remaining accessible to audits and inspectors so you can focus on getting your drug to market and not on finding documents. 

  10. Mastering Scientific Communication Plans Within Medical Affairs 2/6/2025

    Join industry leaders from Anju and 9 Labs for a presentation on the pivotal role of Strategic Communication Plans (SCP) in medical affairs.