ePRO Resources
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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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Achieving A 2.67x Reduction In Study Build Time For An Innovative Neuromodulation Study
12/20/2024
This study explores the potential of Focused Ultrasound Neuromodulation in deepening meditative states, and the platform that helps enhance the overall experience for researchers and participants alike.
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Electronic Hauser Diary For Parkinson's Clinical Trials
12/9/2024
In honor of World Movement Disorders Day, we highlight advances in Parkinson’s disease care. At the 2024 MDS Congress, Signant presented research on electronic diaries for tracking PD patients' functional status.
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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.
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Simple, Cost-Effective Ways To Engage Patients Using eCOA And IRT
9/7/2022
Today, patients are exposed to sophisticated technology, which presents a huge opportunity to elevate engagement. Consider some common elements when initiating engagement during clinical development.
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Paper vs. eCOA: Hard Calculations For Easy Decisions
6/13/2023
Sticker prices often guide purchases, but there's a broader perspective that encompasses total cost. Use this calculator to compare prices of paper COAs or eCOAs, including ePROs, eDiaries, and eClinROs.
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Exploring The Potential Of Non-Consumer Smartphones In Clinical Trials
4/17/2024
We selected and evaluated a non-consumer device, to explore its potential as a reliable tool for home-based ePRO measure administration. Here’s what we learned from this usability testing.
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Choosing The Right eClinRO Solution For Reliable Trial Data
2/21/2025
Electronic clinician-reported outcomes (eClinROs) enhance the quality and consistency of clinical trial data. Discover key factors to consider when selecting an eClinRO provider.
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Veeva eCOA Demo
6/24/2024
See firsthand how this modern build platform, which includes a ‘one-click’ library of pre-validated questionnaires, reduces build times by 75% and means mid-study updates can be actioned in minutes.
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Regulatory Guidance For PRO Strategy In Oncology Trials
11/10/2023
Kelly Dumais, Principal Scientific Advisor, and Jowita Marszewska, Scientific Advisor at Clario eCOA, delve into the specifics of how recent regulatory advancements are influencing PRO Strategy.