eCOA Resources
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Embracing Accessibility: The Future Of Clinical Trials
10/16/2023
Explore the reasons why accessibility stands as a crucial pillar for the prosperity of biopharmaceutical and clinical research, having evolved into an all-encompassing industry imperative.
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eCOA And Digital Platforms Reduce Diabetes Study Startup To 8 Weeks
10/18/2023
See how digital solutions came together to enable faster study startup by 50% for this top pharma company conducting a Phase 3 diabetes study within the weight loss market.
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Reflections From ISOQOL Conference 2024
1/27/2025
Greta van Schoor attended the 31st Annual ISOQOL Conference, where HRQOL leaders shared insights on optimizing eCOA collection, integrating PROs, and digital health in clinical research.
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Optimizing Prader-Willi Syndrome Clinical Trials
10/21/2024
Learn how Signant is helping to mitigate placebo responses and ensuring high-quality data to improve Prader-Willi syndrome (PWS) clinical trial success.
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Go From Three Meetings To One With AI-Enabled eCOA
5/5/2026
Learn how to turn three meetings into one with AI that is streamlining clinical workflows by reducing redundant steps, simplifying site operations, and accelerating data collection.
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Harnessing The Power Of eCOA Technology
11/29/2023
Get an overview of this COA-focused panel at the C3 Summit in London where industry experts and leaders discussed challenges, opportunities, and strategies in clinical trial diversity, centricity, and outcome assessments.
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The New Standard In Participant-Centric Trials
8/21/2025
Clinical technology must serve both scientific rigor and human experience—and Castor is positioning itself at the forefront of this participant-led future.
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Leveraging eCOA To Improve Patient Adherence In Clinical Trials
2/7/2025
Patient adherence is one of the biggest challenges in clinical trials. eCOA solutions offer intuitive and engaging tools that encourage participants to complete their assessments on time.
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Overview Of Central eSource From CRIO
6/18/2025
Central eSource transforms the conduct of clinical trials by replacing disparate, site-specific source templates with a unified, sponsor-designed framework.
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Expanding Flexibility Of eCOA Data Collection With Controlled Interview Mode
1/31/2022
Discover how the interview mode constitutes an additional data entry mode for ePROs when clinical trial participants cannot go to the study site for a scheduled visit.