ePRO Solutions
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Eliminate Barriers To Cancer Research With Clinical Ink ePRO
5/16/2023
Remove the burdens and barriers inherent in clinical trial participation and deliver a more patient-centric experience with Clinical ink’s ePRO.
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Decentralized Clinical Trials: The Future Of Clinical Research
9/26/2022
Our integrated EDC platform, including eConsent, ePRO, RTSM, and DDC, is your gateway to decentralized trials.
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eCOA And ePRO Solutions For Clinical Trials
3/10/2025
Planning to launch a patient-centric decentralized clinical trial? Give your clinical trial patients an app that makes it easy to participate—from anywhere at any time.
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ePRO And Castor Connect
3/19/2024
Gather data directly from the patient—the true source. Empower your team to streamline data collection, making it faster and easier for everyone involved.
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End-To-End Digital Therapeutics Studies Powered By Technology
2/2/2023
Curebase offers a variety of decentralized study models designed and tested for any type of DTx trial.
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A Fast, Customizable, And Cost-Effective ePRO/eCOA Solution For Complex Studies
8/29/2024
Complex studies often require costly customizations and lengthy timelines. Learn how our innovative study designer can streamline study launch, save you time, and reduce costs.
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Electronic Patient-Reported Outcomes
2/23/2023
Increase patient engagement and improve patient experience with TrialMaster ePRO.
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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.
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ePRO For Oncology Studies
5/15/2024
Now introducing a customized ePRO solution designed specifically for oncology studies: a user-friendly app with a streamlined two-step onboarding process.
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Castor-eCOA Clinical Trial Technology
8/21/2025
1,735 eCOA & ePRO Studies Completed
eCOA and ePRO with Enrollment, eConsent, Payments and EDC integrated. Our services cover build, licensing and 24/7 support.
95%+ Patient Compliance Rate
4-8 Weeks to Deploy
190+ Validated Instruments