IQVIA Integrated Complete Consent IRT eCOA

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IQVIA’s integrated eConsent, IRT, and eCOA solution streamlines trial management by eliminating redundant data entry, improving compliance, and accelerating workflows. It simplifies sponsor and site engagement with unified log-ins, harmonized training, real-time reporting, and automated processes. Benefits include faster patient enrollment, improved protocol compliance, and reduced manual errors. A use case showed 1,300 FTE hours saved compared to unintegrated systems. This interoperable platform improves trial orchestration, quality, and patient outcomes.

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Vendor Sheet

IQVIA Integrated Complete Consent IRT eCOA

IQVIA Integrated Complete Consent IRT eCOA

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