ePRO/eCOA Featured Articles

  1. How AI Is Rewriting The Future Of TMF And Clinical Quality 10/29/2025

    Discover how AI is transforming the TMF from a reactive repository into a proactive, intelligent co-pilot for clinical trials.

  2. Following Up: Your Top Questions From Our EHR-To-EDC Integration Webinar Answered 10/23/2025

    We’ve compiled this follow-up with detailed answers to remaining questions, organized by theme to help you explore topics and advance the conversation on seamless EHR-to-EDC integration.

  3. What Sites Wish Tech Vendors (And Sponsors) Heard At SCDM But Probably Didn't 10/8/2025

    During a Society for Clinical Data Management (SCDM) panel discussion, three site-side representatives discussed the challenges clinical research coordinators have executing their clinical duties amid increasingly complex data entry demands.

  4. Driving The Next Wave Of Innovation In Clinical Data Management 10/2/2025

    To better accommodate growing clinical data volume and decentralized trials, many organizations are activating AI-enabled trial tools to enhance workflows and ensure real time data review.

  5. The Dream Is EHR-To-EDC — eSource Is The Wake-Up Call 9/11/2025

    EHR-to-EDC integration promises efficiency but struggles with interoperability, compliance, and site adoption. eSource emerges as the real bridge, with case studies like MSK proving it can cut setup times, boost accuracy, and lighten site workload.

  6. Paving The Way For Sites To Use Their Own Tech 7/17/2025

    The DTRA has released a detailed playbook to help clinical research sites use their own validated technology in sponsor-led trials. The "Bring Your Own Technology" (BYOT) model aims to reduce tech overload at sites, improve efficiency, and preserve regulatory compliance — starting with eConsent as its first use case.

  7. Feasibility/Site Selection Process Ripe For Improvement 4/1/2025

    One key to a more effective feasibility process is more transparent communications and collaboration between sponsors, CROs, and sites. Sponsors must provide clear information to each site to enable a more accurate recruitment assessment, and sites must properly digest the information to give an accurate projection. But how?

  8. RTSM System Customizability Drives Personalized Medicine Trials 1/29/2025

    eClinical experts discuss supply chain management and IRT system design in clinical trials that include personalized medicine elements.

  9. A Year Of Reflection And Preparation 1/3/2025

    The Trial Master File (TMF) landscape in 2025 will require companies to stay attuned to the evolving ICH E6(R3) guidelines and the full implementation of the CTIS.

  10. Plodding Toward Better Data Integration & SSO 10/23/2024

    Laura Hilty, a principal at HealthX Ventures, talks about the need to better integrate data platforms and improve/enable single sign-on (SSO) solutions so sites can lessen their administrative burden.