ePRO Resources

1. 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.

2. Considerations For Implementing The Best eCOAs In Your Trial Design 5/2/2022

   Dive into considerations when deciding on the best COAs to implement as well as best practices when developing your eCOA strategy in this blog.

3. 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.

4. How To Overcome The Problem Of The Early ePRO Oversell 11/14/2022

   In this blog, explore how the approach to PROs needs to be reconsidered, given increasing regulations and trial scrutiny, the clinical need for patient-reported outcomes, and the ability to drive costs down and move off paper.

5. Balancing Clinical Care With Digital Utility In Hybrid Trials 10/24/2022

   To create an effective decentralized clinical trial, tools and methods must be considered within the context of challenges faced by the clinical trial’s patients, physicians, and sites.

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the challenges pharmaceutical companies face in implementing PROs in cancer clinical trials as outlined in the FDA’s draft guidance, as well as strategies to overcome these obstacles.

7. Empowering Freenome: Large-Scale Data Quality And Compliance 10/17/2023

   Delve into five ways this biotech company was able to successfully deliver data quality and compliance for large-scale trials while developing next-generation blood tests for early cancer detection.

8. 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.

9. 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.

10. 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.