E-Technologies STREAM

  1. 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.

  2. Overcoming TMF Management Challenges For Small And Mid-Sized Companies 2/10/2021

    Maintaining an inspection-ready Trial Master File is becoming increasingly burdensome, even for teams with significant resources. In this webinar our experts walk through a new, full-service TMF management approach implemented by smaller biopharmaceutical companies. By adopting a fixed-fee, turnkey model encompassing everything required for ongoing TMF health, these organizations are achieving high-quality TMF compliance – with far less effort.

  3. Customer Testimonial – Keya Watkins, SVP, Oncology, Catalyst 6/26/2024

    Join Keya Watkins, SVP of Oncology at Catalyst, as she discusses the transformative impact of Rave EDC in enhancing competitiveness and sponsor engagement in oncology trials.

  4. Casebook Amendments In Vault EDC 8/27/2021

    Making casebook changes is easy in Vault CDMS, even in active studies. Use the simple, point-and-click interface to deploy changes to specific sites and subjects. Any new forms or fields are then flagged for site personnel to populate retrospectively for existing patients.

  5. 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.

  6. 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.

  7. 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.

  8. Harnessing The Potential Of Patient-Level Data In Clinical Trials   6/19/2024

    Join our panel of industry leaders as they explore innovative methods and best practices for incorporating fully consented patient data in clinical trials.

  9. Industry-First eTMF AI: PhlexTMF v21 4/6/2023

    Pre-trained on millions of documents and embedding the cumulative guidance of Phlexglobal’s TMF experts, uncover how teams can ensure clinical documents are “right-first-time” at document upload.

  10. Do You Know Your TMF Health Score? 3/31/2022

    For inspection-readiness, the critical attributes of TMF health are completeness, timeliness, and quality. View our experts explore what your TMF Health Score could be and how this can be used to achieve and maintain ongoing TMF health and inspection readiness.