ePRO Resources
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On-Site ePRO In Action
3/16/2026
Bridge the gap between clinic and home with flexible data capture. Use any device to ensure consistent, real-time data entry and improve compliance throughout the study lifecycle.
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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.
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Minimizing Hurdles For Patients During The eConsent Process
10/4/2022
Learn how eConsent digitalizes the trial participant consent process through increasingly simplified models designed to improve comprehension and boost engagement.
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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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eCOA Predictions For 2022
5/2/2022
Dive into the prediction that the rapid adoption of eCOAs will continue to grow in 2022, as sponsors acknowledge how useful these tools have become in decentralized clinical trial (DCT) settings.
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Why ePROs In Oncology Are Perfect For Capturing The Patient's Voice
5/15/2025
Recently released FDA guidance showcases why electronic patient-reported outcomes (ePROs) are ideal for capturing the “voice” of the patient. See how ePRO eases oncology trials.
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Headed Down Registry Road? Here Are The EDC Features You'll Need
3/18/2022
Most of us rely on electronic data capture (EDC) to help us reach our study destination. How do we choose the EDC "vehicle" that will get us there safely, with minimal delays? Consider the relative importance of these key EDC features.
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What Universalized Terminology Means For Decentralized Research
10/26/2022
Many DCT stakeholders have attempted to release terminology guides as it relates to their own dealings, however, there had never been a wide range of universalized DCT terms until now.
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How eCOA Improves Data Quality In Clinical Trials
11/20/2024
eCOA solutions enhance data quality in clinical trials by preventing common issues in paper-based COA data, such as missing, ambiguous, or conflicting entries, and ensuring reliable data collection.
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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.