ePRO Resources

  1. Mobile App And Wearable Integration Collects Longitudinal Data 2/12/2024

    Get an overview of SISCAPA's utilization of eTechnologies, specifically ePRO, and how their partnership with CDS accurately demonstrates the improvement of data collection and analysis in the biotechnology industry.

  2. Taking Advantage Of EMA CTR For eCOA Studies In EU 7/13/2023

    Discover how sponsors can save time and effort by applying for clinical trial authorization once across the EU using the Clinical Trials Information System (CTIS).

  3. How A Remote ePRO Solution Helped Reduce Patient Burden 9/19/2022

    Discover how transitioning multiple studies from on-site to at-home assessments improved patient retention and recruitment for a global neurology program.

  4. 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.

  5. Medrio eCOA/ePRO 3/18/2024

    Take your ePRO clinical outcome assessments from clunky to convenient. Intuitive, configurable solutions improve the participant experience, site processes, and data quality, from protocol to postmarket.

  6. 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.

  7. Evidence Generation Evolved 6/13/2024

    Explore how innovative strategies are cutting clinical trial times in half and accelerating the delivery of life-saving treatments.

  8. Where PRO Strategy Goes Wrong 5/27/2026

    PRO and COA strategy is now central to trial success. Organizations that capture meaningful patient experience data will gain stronger evidence and a regulatory advantage.

  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. The Transformative Impact Of EDC Systems In 2025 5/6/2025

    The shift towards decentralized and hybrid trials underscores the significance of EDC in expanding geographic reach, fostering diversity in participant populations, and reduce participant burden.