ePRO Resources

  1. Designing ePRO and eConsent Solutions that Participants and Sites Want 10/26/2022

    Participant-focused eClinical technologies offer significant potential to decrease paper-based processes and improve end-user experiences in collecting patient-reported outcomes (PRO) and informed consent, but many users continue to experience rigid technology, complicated hardware provisioning processes, and clunky implementations that leave sponsors, CROs and sites questioning the value. 

  2. What Universalized Terminology Means For Decentralized Research 10/26/2022

    Many DCT stakeholders have attempted to release terminology guides as it relates to their own dealings, however, there had never been a wide range of universalized DCT terms until now. 

  3. 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.

  4. FDA Pushes For Patient Voice: ePRO In Oncology Trials 1/8/2026

    FDA urges sponsors and CROs to include patient voices in oncology trials. Discover why it matters and how to start integrating this approach.

  5. Empowering Oncology Research With The Right Technology Solutions 10/25/2023

    Explore how advanced technology solutions have the potential to simplify the operational aspects of oncology trials.

  6. Strategies To Minimize Participant And Healthcare Provider Burden 3/21/2025

    Patient-reported outcomes (PROs) are vital for clinical trials but can burden participants and providers. Discover strategies and practical solutions to ease these burdens and improve data quality.

  7. A Blueprint For Modern Obesity Research 5/6/2026

    The landscape of obesity and GLP-1 research has reached a saturation point. To successfully scale to the 5,000-patient registries now required for long-term evidence, a shift in operational architecture is essential.

  8. Why Capturing Pro Data Matters In Early-Phase Oncology Trials 9/26/2024

    If you are in the early stages of an oncology trial, there is a lot to consider when it comes to your data management and how the process can be simplified by improving how your study captures data.

  9. NeuraLace Doubles Clinical Trial Enrollment & Improves Participant Compliance With EDC & ePRO 3/20/2023

    Find out how one company dedicated to producing innovative non-invasive chronic pain therapies was able to engage its patients in new ways.

  10. 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.