E-Technologies STREAM

  1. Maximize Control And Transparency On The Path To Study Go-Live 10/10/2024

    Simplify the historically complicated, black-box processes around eCOA solution deployment, content storage and visualization, and global go-live.

  2. Preparing For 2022 1/19/2022

    2022 will be an important year for drug development. There are many questions around changes that came into play during the pandemic. A panel of experts look back over the year and into the future to help you prepare for the coming year.

  3. Selecting And Expanding Your EDC System: A Testimonial From Everest Clinical Research 4/25/2025

    Everest Clinical Research shares what lead them to strengthen their partnership with Medidata, and expand past the use of Medidata's EDC products too other helpful solutions.

  4. Everything You Need To Know About Adopting eConsent Across Large Pharma Organizations 2/22/2023

    Did you know that the average cost for a delayed trial is between $600,000 and $8 million per day? Discover how electronic consent management technology is helping sponsors, CROs, and sites.

  5. 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.

  6. 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. 

  7. Trials And Tribulations Of Electronic Patient Consent: Removing Barriers To eConsent Adoption 6/3/2021

    After a decade of dabbling with eConsent, how can sponsors and technology providers meet the demand to bring clinical trials directly to the patient at a global scale? In this webinar, you’ll learn strategies to overcome the persistent challenges in eConsent adoption and gain the benefits promised from successful decentralized trials with remote capabilities for patients and sites.

  8. 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.

  9. 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.

  10. Clinical Leader Solutions Expo: eCOA/ePRO 4/3/2024