ePRO Resources

1. Streamlining Clinical Trials: A Guide To Migrating From Paper To EDC 4/19/2023

   Electronic modes have been shown to improve data quality in clinical trials. Address how equivalency can be achieved when migrating PROs from paper to ePRO.

2. Exploring Modular Mobile And Web ePRO 10/17/2023

   Review the capabilities of this collection of ePRO applications, available on both web and mobile platforms, for enhancing hybrid or decentralized clinical trial experiences.

3. Empowering Caregivers With ePRO Technology For Cancer Support 5/16/2023

   Explore the importance of involving caregivers in the care process and how electronic patient-reported outcomes technology can facilitate communication, tracking, and collaboration.

4. Designing ePRO and eConsent Solutions that Participants and Sites Want 10/26/2022

   Participant-focused eClinical technologies offer significant potential to decrease paper-based processes and improve end-user experiences in collecting patient-reported outcomes (PRO) and informed consent, but many users continue to experience rigid technology, complicated hardware provisioning processes, and clunky implementations that leave sponsors, CROs and sites questioning the value. 

5. Empowering Oncology Research With The Right Technology Solutions 10/25/2023

   Explore how advanced technology solutions have the potential to simplify the operational aspects of oncology trials.

6. 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.

7. What Is eCOA And How Does It Improve Clinical Trial Data Quality? 4/14/2023

   Discover how eCOA data capture can improve clinical trials by providing improved data quality, regulatory compliance, and accelerated clinical development.

8. Gain The ePRO Advantage With Real-Time Data Collection 12/2/2022

   Discover how ePRO automatically incorporates eCOA data into a study, improving the depth, timeliness, and accuracy of patient-reported outcomes data in the following ways.

9. Safety Monitoring: What Does ePRO Have To Do With It? 1/10/2022

   In the available blog post, learn about the importance of safety monitoring in clinical trials.

10. 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.