Patient Data Reporting White Papers & Articles

  1. How EDC-Based SAE Reporting Reduces Time To Detection And Response 7/7/2025

    Serious adverse events (SAEs) play a pivotal role in patient safety during clinical trials, and the right EDC system helps you efficiently track and manage the entire lifecycle of SAE reporting.

  2. Central eSource Is The Latest In Sponsor Provided Site Offerings 7/7/2025

    For decades, sponsors have provided tools to help clinical sites work more efficiently. Central eSource is the latest evolution in this trend.

  3. eSource Purpose Is Not Just To Complete The EDC 7/7/2025

    Central eSource transforms data capture from a passive, back-end chore into an active, real-time quality and compliance engine—delivering benefits that extend beyond faster EDC feeds and reduced SDV.

  4. How Site eSource Completes And Extends The EHR To EDC Initiative 7/7/2025

    This study evaluates to what degree an eSource-to-EDC data transfer initiative succeeds through two key dimensions: "Mappability" and "Prevalence".

  5. It's Official: CRIO Sites Are Now 25% Of US Sites On Chronic Condition Studies 7/7/2025

    CRIO continues to lead the U.S. eSource market, with its platform widely adopted across clinical research sites. A recent analysis of 50 Phase 2 and 3 studies showed that, on average, 28% of U.S. sites were CRIO clients, with even higher adoption in key therapeutic areas.

  6. How Sponsors Can Drive Success With Central eSource At Investigator Sites 6/17/2025

    Centralized eSource systems enable complex clinical trials to align with key regulatory frameworks, including ICH E6(R3), ICH E8(R1), and 21 CFR 312, to meet the highest standards of GCP.

  7. Innovations In Pediatric Depression Assessment 6/17/2025

    Discover the transformation of a complex assessment challenge into a competitive advantage. Our electronic CDRS-R doesn't just digitize the scale—it embeds clinical expertise, automates quality controls, and guides raters through every step to ensure consistent, reliable data.

  8. EHR-To-EDC Success In A Complex Oncology, Adaptive Platform Trial 6/10/2025

    The I-SPY 2 Trial represents a groundbreaking approach in oncology, with a key component of the trial's success being the integration of EHR with EDC via OpenClinica's Unite platform.

  9. eSource vs. EDC: Reimagining Your Clinical Trials 5/29/2025

    Explore how an eSource approach to clinical trial data can reduce site burden, eliminate double data entry, minimize queries, and enhance remote monitoring.

  10. Reimagining The Protocol For The Future Of Research 5/23/2025

    Clinical trial protocols are the blueprints of research, yet they remain locked in static, text-based documents that must be manually reinterpreted across each clinical system.