ePRO Resources

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the challenges pharmaceutical companies face in implementing PROs in cancer clinical trials as outlined in the FDA’s draft guidance, as well as strategies to overcome these obstacles.

  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. Why eConsent Makes Such A Difference In Patient Adherence And Engagement 6/6/2022

    Explore how consent is a critical step that can greatly influence patient enrollment, adherence and retention in the trial.

  4. The Future Of Clinical Trials Rests On A Unified CTMS Platform 8/1/2022

    Discover why a unified CTMS platform is the answer for managing both the clinical trial itself and the data it produces when it comes to poorly integrated clinical trial management systems (CTMS).

  5. Simplifying ePRO Data Collection 10/4/2024

    The Bring Your Own Device (BYOD) model, supported by Trialkit, is an innovative approach in clinical trials that allows participants to use personal smartphones or tablets for data collection.

  6. 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.

  7. The Benefits Of Real-Time ePRO/eCOA In Clinical Trials 10/4/2024

    TrialKit addresses data management issues in clinical trials through its innovative ePRO and eCOA tools, which facilitate real-time data collection and reporting.

  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. 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.

  10. Achieving A 2.67x Reduction In Study Build Time For An Innovative Neuromodulation Study 12/20/2024

    This study explores the potential of Focused Ultrasound Neuromodulation in deepening meditative states, and the platform that helps enhance the overall experience for researchers and participants alike.