eConsent Solutions
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A Clinical Research Toolset That Delivers Power And Ease Of Use
1/23/2024
Improve experiences and outcomes in clinical trials with a robust, and modern toolset of best-in-class solutions for eSource, ePRO, data capture, reporting, and more.
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Get Your Tile Into One Home
7/15/2024
For clinical trial technology vendors, it’s fast and easy to become part of the only industry-wide solution to sit tech overload.
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Improving The Patient Experience With Total Consent
11/6/2023
Increased outreach, heightened involvement, superior quality. Tour this comprehensive consent management solution that enhances participant access and improves the overall patient experience.
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Modern eConsent Built For Clinical Research Sites
6/24/2026
We partnered with leading academic medical centers, sponsors, hospital systems, and site networks to create an eConsent platform that is easy-to-use and minimizes risk.
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Patient Engagement By Datacubed Health
2/16/2022
Explore how the Datacubed platform supports eCOA, virtual visits, eConsent and geofencing (a frictionless way to capture adverse event data) in one solution.
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Simplifying The Patient Journey With One App
11/12/2025
A single mobile app simplifies clinical trial participation by unifying eConsent, IRT, and eCOA workflows, reducing patient burden and improving engagement across trial phases and locations.
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EDC: Control Your Data, Control Your Study
2/16/2023
Streamline data, maximize efficiencies, tighten up costs, and reach end goals faster using Medrio’s powerful and intuitive EDC tool.
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Just The Facts: Direct Data Capture
5/20/2022
Start enabling direct data capture (DDC), clinical outcome assessments (eCOA), patient reported outcomes (ePRO), and eConsent with the Clinical ink platform.
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It's Time To Move Into One Home for Sites
10/7/2025
Explore a vendor- and sponsor-neutral platform that streamlines trial management by consolidating systems and tasks.
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Why Choose TrialKit For Your Clinical Trials?
7/18/2024
TrialKit supports everything from small biologics trials to large Phase 3 pharmaceutical trials and extensive registry studies, allowing you to capture and manage your clinical trial data as you see fit.