ePRO Solutions
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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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Instill Greater Confidence In Respiratory Data
11/13/2023
Discover how this solution is improving data quality and helping clinical trial teams to "breathe easy" throughout their pulmonary and other lung safety or disease studies.
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Veeva eCOA Features Brief
6/24/2024
Ensure access and transparency throughout clinical studies while streamlining the design, management, and completion of electronic Clinical Outcome Assessments with Veeva eCOA.
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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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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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Democratizing Clinical Research With Castor
5/11/2023
Execute your study with Castor using modular solutions or as a platform package.
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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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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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Your Biometrics CRO Partner
10/30/2023
Explore the ways that this dedicated team of experts with unwavering knowledge and expertise meticulously cares for and manages clinical trial data.