EDC/Data Management White Papers & Case Studies

  1. Real-Time Clinical Data Insights Delivered By Automation And AI 2/26/2026

    Automated data flows and human‑guided AI enable faster, more reliable oversight into clinical trials. Learn how real‑time insights and unified monitoring support quality, efficiency, and readiness.

  2. The Hardest Trials Deserve The Easiest Solutions 2/13/2026

    Explore practical ways to simplify complex oncology studies with unified data, streamlined workflows, and more supportive patient and site experiences.

  3. State Of Clinical Trial Technology: The AI Inflection Point 2/12/2026

    Digital maturity gaps are widening in clinical research. Connected workflows speed insights and execution, while manual processes leave organizations increasingly behind.

  4. Unify Workflows And Accelerate Execution From Protocol To Submission 2/2/2026

    Explore a platform that benefits the entire global clinical trial ecosystem by reducing complexity and operational costs while maintaining the highest standards of data security and subject privacy.

  5. Your Medical Imaging Workflow Solution 2/2/2026

    By addressing common "pain points" such as the complex handling of DICOM files and unreliable transfer methods, the Judi platform prevents workflows from coming to a grinding halt.

  6. Rave TSDV - Improve CRA Efficiency And Reduce Site Burden 1/5/2026

    Source data verification (SDV) is a critical activity within clinical trial monitoring, yet the traditional approach focused on 100% SDV is limited in its ability to quickly identify issues and prevent them from recurring. Rave TSDV (Targeted SDV), unified with Rave EDC, enables CRAs to focus on critical to quality (CtQ) factors identified within risk management activities.

  7. Accelerating Clinical Data Review With Traceable Workflows 12/3/2025

    Clinical data review needs centralized access and traceable workflows. Leveraging AI-automation and real-time collaboration drives faster, better-informed decisions and reduced compliance risk.

  8. Generate Regulatory-Grade, RWE With Speed And Efficiency 11/21/2025

    For teams managing real-world evidence or post-market studies, automation offers a scalable solution to streamline workflows, maintain compliance, and accelerate decision-making.

  9. Driving A High-Adherence LTFU Trial Without An EDC 10/29/2025

    Discover how our partnership with a client was able to deliver a ten-year long-term follow-up (LTFU) trial that delivered an over 90% adherence rate while keeping trial costs low by not using an EDC.

  10. Improving Clinical Trial Performance Through Central eSource 10/23/2025

    See how a top five pharmaceutical company leveraged our esource platform to enhance site performance, improve data consistency, and enable remote monitoring.