ePRO Resources

31. An ePRO Platform Designed With Real People In Mind 4/6/2023

    With a combination of technology and consultative support from team experts, start experiencing a seamless ePRO transition and establish a smoother path to regulatory submission today.

32. Focusing On Patient-Reported Outcome Measures And eConsent 8/7/2023

    Learn how digital solutions can contribute to a more participant-centered approach and potentially enhance the regulatory utility of PRO data while improving the overall quality and efficiency of oncology trials.

33. Headed Down Registry Road? Here Are The EDC Features You'll Need 3/18/2022

    Most of us rely on electronic data capture (EDC) to help us reach our study destination. How do we choose the EDC "vehicle" that will get us there safely, with minimal delays? Consider the relative importance of these key EDC features.

34. Increase Participant Diversity With eClinical Tools 4/14/2023

    The right technology and community partnerships can help sponsors meet FDA diversity requirements without additional expenditures, build relationships with minorities, and prepare for future trials.

35. Interview Mode: A Valuable Data Collection Alternative Supporting DCTs 3/8/2022

    Download the available infographic to discover how collecting ePRO & eObsRO data via interview mode can be recommended in specific circumstances.

36. 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.

37. Reflections From ISOQOL Conference 2024 1/27/2025

    Greta van Schoor attended the 31st Annual ISOQOL Conference, where HRQOL leaders shared insights on optimizing eCOA collection, integrating PROs, and digital health in clinical research.

38. Overcoming Oncology Trial Challenges With ePRO Solutions 5/16/2023

    Discover effective strategies and solutions to overcome challenges in oncology studies and how to optimize trial design, patient recruitment, data management, and regulatory compliance.

39. Leveraging Tech And Clinician Review To Improve Risk Detection 10/19/2023

    Learn why neuroscience therapy developers should start adopting strategies to improve data quality and assess responses using a combination of technology and expert clinician review.

40. Paying Sites To Reduce Burden 6/12/2026

    Beth Harper and Rosie Filling discuss site burden, enrollment pressure, and why sponsors should help pay for technology and training.