E-Technologies STREAM

  1. The Art Of Accelerated Study Closeout: End Of Study Solutions 11/2/2023

    Watch as experts from eClinical Solutions and Medidata delve into end-of-study process challenges, the transition to electronic distribution and management, the advantages of leveraging a digital platform, and more.

  2. Align eDiary Design With Assessment Schedules 4/2/2025

    Ensure alignment with your study protocol by leveraging the Sculptor portal to simulate eDiary completion and top-down scheduling, allowing for real-time preview and modifications.

  3. Notifications And Reminders 3/27/2025

    Configurable alarms appear as banner alerts on subjects’ devices, while email notifications help sites monitor potential non-compliance and respond to newly uploaded symptom severity data.

  4. Rapid Study Design With The Sculptor Portal 4/2/2025

    Accelerate your eCOA assessment design to streamline UAT, mid-study updates, and protocol amendments effortlessly.

  5. 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.

  6. 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.

  7. Customer Testimonial – Chuck Bradley, Clinical Development & Operations Consultant 6/26/2024

    In this testimonial, a Clinical Development & Operations Consultant highlights the industry-standard Medidata platform and the significant benefits of using a consistent system across sites.

  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. 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. 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.