ePRO Resources

  1. 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.

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the challenges pharmaceutical companies face in implementing PROs in cancer clinical trials as outlined in the FDA’s draft guidance, as well as strategies to overcome these obstacles.

  3. Paper vs. eCOA: Hard Calculations For Easy Decisions 6/13/2023

    Sticker prices often guide purchases, but there's a broader perspective that encompasses total cost. Use this calculator to compare prices of paper COAs or eCOAs, including ePROs, eDiaries, and eClinROs.

  4. eCOA 101: Why Choose ePRO vs. Paper 9/18/2024

    ePRO solutions enhance data quality, operational efficiency, and patient-centricity in clinical trials by allowing patients to report outcomes digitally instead of using pen and paper.

  5. Choosing The Right eClinRO Solution For Reliable Trial Data 2/21/2025

    Electronic clinician-reported outcomes (eClinROs) enhance the quality and consistency of clinical trial data. Discover key factors to consider when selecting an eClinRO provider.

  6. Why ePROs In Oncology Are Perfect For Capturing The Patient's Voice 5/15/2025

    Recently released FDA guidance showcases why electronic patient-reported outcomes (ePROs) are ideal for capturing the “voice” of the patient. See how ePRO eases oncology trials.

  7. Measuring The True Patient Experience 5/15/2024

    Utilizing the insights covered in this article can inform the design and implementation of cancer trials, ultimately contributing to improved patient care and treatment outcomes.

  8. Regulatory Guidance For PRO Strategy In Oncology Trials 11/10/2023

    Kelly Dumais, Principal Scientific Advisor, and Jowita Marszewska, Scientific Advisor at Clario eCOA, delve into the specifics of how recent regulatory advancements are influencing PRO Strategy.

  9. 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.

  10. Rethinking Today's ePRO Delivery For Tomorrow's Clinical Trials 6/24/2024

    Willie Muehlhausen, Co-CEO and Founder of Safira Clinical Research, and Tim Davis, VP of Strategy at MyVeeva for Patients, discuss how ePRO delivery needs to change to better serve modern trials.