eCOA Resources
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Still Using Paper Diaries To Capture PRO Data? Read This.
1/8/2024
Access real-world examples of how electronic patient-reported outcome measures (PROMs) optimize data quality and reliability and improve the statistical power of trial data.
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Medrio eCOA/ePRO
3/18/2024
Take your ePRO clinical outcome assessments from clunky to convenient. Intuitive, configurable solutions improve the participant experience, site processes, and data quality, from protocol to postmarket.
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Accelerating CRO Study Deployment At Scale
7/7/2025
A top-3 CRO and a top-10 pharmaceutical company partnered with Medable to help accelerate, scale, and standardize their eCOA trials. See how they accomplished it.
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A Definitive Guide To Evidence Generation
10/18/2023
Obtain a complete understanding of enrollment, screening, consent, and data collection by diving into this introductory handbook on decentralized clinical trials.
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Potential Of eClinical Solutions To The Complexity Of Oncology Trials
7/31/2025
How are eClinical technologies—specifically IRT and eCOA— being leveraged to overcome patient recruitment difficulties, high mortality rates, and the intricacies of cancer treatments.
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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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Simplify Your Clinical Data Flow To Streamline And Automate Modern Data Review
11/11/2022
Examine the three reasons why simplifying your clinical data flow can increase operational oversight, shorten data management cycle times, and reduce the manual burdens on data management teams.
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Smarter eCOA With Clinical ink
9/22/2022
Deploy a smarter, faster, simpler eCOA with Clinical ink, powered by deep outcomes science expertise across many therapeutic areas.
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Patient First Solutions For Oncology
2/14/2023
Medable, Inc's new oncology offering is an end-to-end suite that includes an extensive eCOA library, pre-built and validated DCT applications such as Total Consent and Televisit, and protocol design consulting.
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How Site And Patient Research Optimizes Clinical Trials
6/17/2024
Signant’s patient and site research enhances digital health technology in clinical trials by optimizing usability and design. These insights drive improvements in product features, study designs, and training materials.