ePRO Resources
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Why eConsent Makes Such A Difference In Patient Adherence And Engagement
6/6/2022
Explore how consent is a critical step that can greatly influence patient enrollment, adherence and retention in the trial.
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The Benefits Of Real-Time ePRO/eCOA In Clinical Trials
10/4/2024
TrialKit addresses data management issues in clinical trials through its innovative ePRO and eCOA tools, which facilitate real-time data collection and reporting.
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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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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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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.
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Mobile App And Wearable Integration Collects Longitudinal Data
2/12/2024
Get an overview of SISCAPA's utilization of eTechnologies, specifically ePRO, and how their partnership with CDS accurately demonstrates the improvement of data collection and analysis in the biotechnology industry.
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Designing ePRO And eConsent For Pediatric Trials
8/29/2024
Gain confidence in making your next pediatric trial more successful by leveraging the technology discussed to address common challenges in pediatric studies.
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Streamlining Clinical 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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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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Can Your Clinical Trial Design Handle Mid-Study Changes?
9/25/2023
Mid-study changes are frequently inevitable, but it’s possible to reduce the downtime they create with strategic planning and technology. See how to plan for mid-study changes that mitigate downtime.