E-Technologies STREAM

  1. Building One Home for Sites 7/23/2024

    Watch this presentation and demonstration of One Home for Sites for the latest updates on how the industry is coming together — even competitors — to alleviate the technology burden on research sites.

  2. 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.

  3. Deploy eConsent Around The World With Confidence 8/16/2022

    Explore an easy, secure way to deliver highly engaging, regulatory-compliant electronic consent for trials of all types with IQVIA Complete Consent.

  4. Successful Subject Creation With eCOA, eConsent, & IRT Process Flow 5/26/2023

    Watch a short walkthrough of how IRT and electronic Clinical Outcome Assessment (eCOA) solution on a unified platform delivery drives smoother study orchestration.

  5. 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.

  6. Defining And Implementing The Right Oncology Digital Strategy 11/7/2024

    A panel of oncology experts shares how top life science companies are using a combination of DHTs, ePROs, clinical trial platforms, and more to ease oncology research and drastically reduce timelines.

  7. Optimal eCOA For Vaccine Trials 8/23/2023

    Delve into the pivotal role that technologies like electronic Patient-Reported Outcomes (ePRO) can play in generating substantiating evidence and streamlining vaccine trial operations.

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

    Delve into the art of tailoring the eConsent experience to match your study and patients' specific needs, such as crafting eConsent documents, selecting appropriate delivery models, and more.

  9. Overview Of Central eSource From CRIO 6/18/2025

    Central eSource transforms the conduct of clinical trials by replacing disparate, site-specific source templates with a unified, sponsor-designed framework.

  10. Selecting Medidata Rave: A Testimonial From Richmond Pharmacology 4/25/2025

    What made the Medidata's Rave EDC system stand out to Richmond Pharmacology during their vendor selection period?