ePRO Resources
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Streamlining Trials: How To Upgrade 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.
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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.
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Measuring The True Patient Experience
5/15/2024
Utilizing the insights covered in this article can inform the design and implementation of cancer trials, ultimately contributing to improved patient care and treatment outcomes.
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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.
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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.
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Paper Vs ePRO: Clinical Data Collection Methods
7/16/2024
Patient-reported outcomes (PROs) assess patients' health without clinician interpretation. Traditional paper methods often result in missing data and quality issues, while electronic solutions enhance data accuracy and completeness.
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Pharmaceutical Company Gets Unified Decentralized Platform
2/28/2023
Unearth how this global eClinical provider delivered a decentralized platform including eSource/ePRO for direct-data-entry, randomization, eConsent, telehealth, remote monitoring, and data management.
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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.
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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.
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What Is ePRO?
3/30/2026
Real-time patient reporting improves data quality and trial insight. Digital tools cut missing data, enable remote participation, and clarify how treatments affect daily life.