ePRO Resources

  1. 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.

  2. 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.

  3. Redefining Evidence Generation In Modern Clinical Trials 8/2/2024

    As trials continue to digitize, learn how connected sensors, COAs, PROs, and other forms of data will come together to form the evidence of tomorrow.

  4. Own Your Data, Accelerate Your Cure 5/6/2026

    Move from passive donor to active innovator. Explore how patient communities are building their own research infrastructure and using AI to bypass traditional barriers to drug development.

  5. 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.

  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. 3 Steps To Improve Site Acceptance Of ePRO In Medical Device Trials 3/6/2023

    Discover how with the proper understanding of a site’s barriers, early engagement, and prioritizing effective training, site acceptance of ePRO can be improved.

  8. 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).

  9. Addressing The Specific Complexities Of Oncology eCOA Clinical Trials 4/18/2022

    What are the specific tools and keys to conduct eCOA trials in oncology successfully? This article identifies some of the relevant solutions to tackle oncology protocol complexities.

  10. 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.