E-Technologies STREAM

  1. At The Crossroads Of Data: eCOA And Sensors Converging For Novel Insights 5/20/2025

    Leveraging sensors and eCOA addresses increasing clinical trial complexity and ensures a more efficient and effective study design.

  2. Customer Testimonial – From CRA To Management 6/26/2024

    Join Brittany Erlandson, Sr. Manager of Clinical Operations at QuidelOrtho, as she shares her journey from CRA to management and the crucial role of Medidata's EDC system in enhancing efficiency.

  3. 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.

  4. 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?

  5. Transform Your Clinical Trials With Central eSource 3/25/2026

    Accelerate your trial startup and reduce site burden with a central eSource that allows sponsors to develop and publish central source templates to sites.

  6. 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. 

  7. The Diversity Imperative: EDC And Inclusive Clinical Trials 3/4/2024

    In this EDC Showcase, experts delve into the crucial role of EDC in fostering diversity within clinical trials. Discover adaptable solutions for a more inclusive and efficient clinical workflow.

  8. 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.

  9. Should Sponsors Provide Source Document Templates? 12/9/2025

    Here, we debate sponsor-provided source document templates, weighing regulatory guidance, compliance risks, and operational impacts for smarter clinical trial documentation decisions.

  10. Using Technology To Reduce Monitoring Costs And Increase Quality 2/18/2025

    Join industry experts as they discuss how the true value of DDC lies not just in the cost of the technology itself but in the operational efficiencies it unlocks.