ePRO Resources

  1. Expanding Flexibility Of eCOA Data Collection With Controlled Interview Mode 1/31/2022

    Discover how the interview mode constitutes an additional data entry mode for ePROs when clinical trial participants cannot go to the study site for a scheduled visit.

  2. The Building Blocks Of DCT: How To Create A Seamless Experience Across eConsent, eCOA, And More 3/29/2022

    With more than 76% of sponsors seeking to implement decentralized solutions this year, there’s never been more attention given to decentralized trials. Discover why decentralized trials must take a unified approach, one that alleviates burdens for patients and sites in order to drive cost savings and realize efficiencies. 

  3. 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.

  4. Rare Disease Clinical Trials: Modern Design And Supply Chain 10/12/2023

    Gain insight from several contributing experts for overcoming unique obstacles in rare disease research and learn how to better develop strategies.

  5. 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.

  6. How Data Collection Is Enabling CROs To Expand Service Offerings 9/22/2022

    Explore how innovative processes and advanced data collection technologies like ePRO and eCOA can help contract research organizations expand their service offerings.

  7. eCOA/ePRO: Why Patients Deserve Even More Progress 5/11/2022

    The shift from reporting on paper to reporting electronically has been happening for years, however, the transition hasn’t always been elegant. Explore how the pandemic has played a role in accelerating the shift to eCOA/ePRO.

  8. Revolutionizing Pediatric Clinical Trials With ePRO And eConsent 10/16/2024

    Digital tools like ePRO and eConsent are essential in addressing pediatric trial challenges such as the diverse participant ages and family involvement, which impact retention and data quality.

  9. The New Standard In Participant-Centric Trials 8/21/2025

    Clinical technology must serve both scientific rigor and human experience—and Castor is positioning itself at the forefront of this participant-led future.

  10. Considerations For Implementing The Best eCOAs In Your Trial Design 5/2/2022

    Dive into considerations when deciding on the best COAs to implement as well as best practices when developing your eCOA strategy in this blog.