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Electronic informed consent (eConsent) improves the experience for patients, caregivers, and clinical-trial staff — yet adoption remains hindered by several barriers. This article reviews the data substantiating eConsent’s positive impact on clinical trial outcomes and what's slowing uptake.
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Traditionally, IRT systems have not been used in early phase trials due to time and cost. However, as early phase studies become more complex, sponsors are re-evaluating the use of IRT. This piece outlines how one IRT solution can increase control, ease-of-use, and cost efficiencies versus manual processes.
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Watch a short walkthrough of how IRT and electronic Clinical Outcome Assessment (eCOA) solution on a unified platform delivery drives smoother study orchestration.
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As part of the inaugural Clinical Leader Solutions Showcase, IQVIA's Dan Pavitt explores the latest innovative techniques in trial design, delivery, conduct, and monitoring of clinical trials, plus a live demonstration of IQVIA’s mobile IP product.
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