CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
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Why Clinical Trial Technology Often Redistributes Work, Not Reduces It
A Duke research program leader breaks down where trial technology genuinely saves site staff time and where it just relocates the same work.
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The 'Swivel Chair' Problem Slowing Down Clinical Trials
A community hospital research director explains why trial data still can’t flow between the EMR and sponsor EDC systems, and what would fix it.
ECOA RESOURCES
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Joe Dustin explains why validation documentation and sponsor benefit are key to getting approval for site-system integration.
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Learn how the right eCOA system enables site efficiency and elevated data quality, ensuring trials run smoothly and deliver more reliable results.
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Explore how the use of electronic Clinical Outcomes Assessments (eCOAs) can be rapidly implemented to capture patient reported outcomes (PROs).
ECONSENT RESOURCES
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Read this blog to learn more about how eConsent can enhance participant engagement and retention when used both onsite and remotely.
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Joe Dustin explains why validation documentation and sponsor benefit are key to getting approval for site-system integration.
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Discover how DCTs leverage “virtual” tools, such as telemedicine, sensory-based technologies, wearable medical devices, and direct delivery of study drugs and materials to patients’ homes.
EPRO RESOURCES
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We selected and evaluated a non-consumer device, to explore its potential as a reliable tool for home-based ePRO measure administration. Here’s what we learned from this usability testing.
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Discover how harnessing Patient Reported Outcomes electronically in early-phase trials can boost patient centricity, create more cost-effective operations, and help generate better data faster.
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Recently, early-phase protocols have been collecting patient-reported outcomes (PROs) not only to get regulatory approval but to demonstrate value to public and private payers.