ePRO/eCOA White Papers & Case Studies

  1. Addressing Trial Design Hurdles Across Alzheimer’s Disease Stages 12/10/2025

    Explore how endpoint selection, rater training, and the strategic implementation of eCOA can help address the unique scientific, operational, and human considerations at each stage of AD.

  2. Study Analysis – Site Payment Automation 12/8/2025

    By removing administrative bottlenecks, see how automation improves cash flow for sites, reduces operational burden for sponsors, and supports smoother, more predictable trial execution.

  3. The Real Cost In CNS Trials: Rater Drift And Site Readiness 11/21/2025

    Learn how to build resilience into CNS trial operations with evidence-based frameworks that prioritize human factors alongside digital tools.

  4. Hospital-Based eCOA Implementation: Real Challenges In Infectious Disease Trials 11/21/2025

    This resource outlines proven strategies to reduce delays, improve compliance, and meet regulatory standards for PRO data in infectious disease studies.

  5. 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.

  6. Simplifying The Patient Journey With One App 11/12/2025

    A single mobile app simplifies clinical trial participation by unifying eConsent, IRT, and eCOA workflows, reducing patient burden and improving engagement across trial phases and locations.

  7. 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.

  8. Greenphire Clinical Finance: Budgeting & Benchmarking 10/23/2025

    Streamline trial budgets and payments with real-time fair market data, speeding startups and ensuring timely, transparent site funding worldwide.

  9. The EMR Interoperability Dream Vs. Clinical Research Reality 10/20/2025

    Seamless Electronic Medical Record access promises accelerated trials and regulatory-grade evidence, but incomplete, unstructured data requires hybrid strategies using AI and human oversight to bridge gaps.

  10. The Hidden Problem In Early Phase Oncology Trials 9/23/2025

    Integrating patient-reported outcome measures (PROMs) can enable improved capture tolerability and optimize dosing decisions.