ePRO Resources

  1. ePROs: How They're Transforming Oncology Research 10/30/2023

    ePRO and eCOA are helping to overcome oncology-specific challenges in clinical research. Find out how you can make life easier for patients when it matters most.

  2. The Transformative Impact Of EDC Systems In 2025 5/6/2025

    The shift towards decentralized and hybrid trials underscores the significance of EDC in expanding geographic reach, fostering diversity in participant populations, and reduce participant burden.

  3. Veeva eCOA Demo 6/24/2024

    See firsthand how this modern build platform, which includes a ‘one-click’ library of pre-validated questionnaires, reduces build times by 75% and means mid-study updates can be actioned in minutes.

  4. Mobile App And Wearable Integration Collects Longitudinal Data 2/12/2024

    Get an overview of SISCAPA's utilization of eTechnologies, specifically ePRO, and how their partnership with CDS accurately demonstrates the improvement of data collection and analysis in the biotechnology industry.

  5. Nevro Eliminates Majority Of Source Data Verification With ePRO And EDC 2/23/2023

    Read how a global medical device company was able to unlock new efficiencies by implementing data collection via electronic patient-reported outcome assessments.

  6. Empowering Freenome: Large-Scale Data Quality And Compliance 10/17/2023

    Delve into five ways this biotech company was able to successfully deliver data quality and compliance for large-scale trials while developing next-generation blood tests for early cancer detection.

  7. Mitigating The Risks Of Long-Term Oncology eCOA Clinical Trials 6/23/2022

    This article digs into the specific complexities of long oncology clinical trials and describes relevant solutions to manage the risks regarding patient compliance, clinical project teams, and clinical sites.

  8. Reduce Patient Burden — And Make The Most Of Valuable Data 7/15/2024

    As actigraphy continues to advance, explore how improvements in device comfort and usability will enhance patient compliance, further optimizing its pivotal role in clinical research across various therapeutic domains.

  9. How To Overcome The Problem Of The Early ePRO Oversell 11/14/2022

    In this blog, explore how the approach to PROs needs to be reconsidered, given increasing regulations and trial scrutiny, the clinical need for patient-reported outcomes, and the ability to drive costs down and move off paper.

  10. What Is eCOA And How Does It Improve Clinical Trial Data Quality? 4/14/2023

    Discover how eCOA data capture can improve clinical trials by providing improved data quality, regulatory compliance, and accelerated clinical development.