ePRO Resources

31. 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. 

32. Rose Research Center Leans On Medrio To Simplify Workflows And Study Design 2/2/2023

    After experiencing paper processing issues, discover how a company transitioned to digital data collection by using Electronic Data Capture (EDC) and Electronic Patient Reported Outcomes (ePRO) solutions.

33. 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.

34. ISR Report Sheds Light On eCOA/ePRO Market Dynamics 5/15/2024

    This comprehensive overview highlights the critical role these platforms play in modern clinical research, emphasizing their impact on data integrity and trial efficiency.

35. 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.

36. Benefits Of Using ePRO In Early Phase Studies 3/24/2023

    Discover how harnessing Patient Reported Outcomes electronically in early-phase trials can boost patient centricity, create more cost-effective operations, and help generate better data faster.

37. The Building Blocks Of DCT: How To Create A Seamless Experience Across eConsent, eCOA, And More 3/29/2022

    With more than 76% of sponsors seeking to implement decentralized solutions this year, there’s never been more attention given to decentralized trials. Discover why decentralized trials must take a unified approach, one that alleviates burdens for patients and sites in order to drive cost savings and realize efficiencies. 

38. Why Standards Matter At Scale 6/12/2026

    Joe Dustin shows why custom integrations do not scale and why standards are essential for efficiently connecting many sites.

39. Modernizing Clinical Research With AI And Digital Data 3/7/2025

    Discover how ActiGraph is revolutionizing clinical trials with patient-focused digital data and cutting-edge technology that enhances trial efficiency across all phases.

40. 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.