ePRO Resources

  1. Site Perspectives On BYOD ePRO Use 6/17/2024

    This study examines participant convenience and compliance, aiming to understand and address the challenges faced by site personnel in global trials.

  2. 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.

  3. 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. 

  4. The Evolution Of Data Capture And Its Impact On Management 12/7/2022

    As the volume and variety of clinical trial data have exploded - including electronic health records (EHR), sensors, and ePRO data - processes to manage and monitor that data have not kept pace. These processes are still grounded in a retroactive data review and reconciliation with a primary focus on eCRF data.

  5. End-To-End Clinical Data Flow 6/24/2024

    Explore the interconnected data flow across Veeva Vault EDC, Veeva CDB, Veeva RTSM, and Veeva ePRO to visualize how these products work together seamlessly.

  6. Designing ePRO And eConsent For Pediatric Trials 8/29/2024

    Gain confidence in making your next pediatric trial more successful by leveraging the technology discussed to address common challenges in pediatric studies.

  7. Streamlining Trials: How To Upgrade From Paper To EDC 4/19/2023

    Electronic modes have been shown to improve data quality in clinical trials. Address how equivalency can be achieved when migrating PROs from paper to ePRO.

  8. 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.

  9. ePRO's Impact On Patient And Site Journeys 5/15/2024

    Join our solutions experts as they demonstrate how Castor ePRO can enhance your clinical trial by improving the patient experience and streamlining site operations.

  10. 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.