ePRO Resources

  1. Safety Monitoring: What Does ePRO Have To Do With It? 1/10/2022

    In the available blog post, learn about the importance of safety monitoring in clinical trials.

  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. 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.

  4. Solutions For Sponsors Utilizing Drafted Guidance For PROs In Oncology 11/20/2024

    Explore the challenges pharmaceutical companies face in implementing PROs in cancer clinical trials as outlined in the FDA’s draft guidance, as well as strategies to overcome these obstacles.

  5. Could ePRO Be The New Standard In Health Reimbursement? 1/30/2023

    Recently, early-phase protocols have been collecting patient-reported outcomes (PROs) not only to get regulatory approval but to demonstrate value to public and private payers.

  6. 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.

  7. 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.

  8. Guide: How Connected Devices Improve Clinical Trial Data 5/29/2024

    Gain an overview of how and why connected devices provide sponsors and CROs with better clinical trial data, and offer patients much better trial experiences!

  9. 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.

  10. Why eSource: The Advantages of Abandoning Paper Records 2/16/2023

    Eliminate transcription errors and fully leverage supporting eClinical technology to provide a reliable consistent exchange of information.