Integrated eClinical Platforms: Why Connected Clinical Trial Workflows Matter
Integrated clinical platforms unify disconnected eClinical systems into seamless workflows. They maintain real-time synchronization throughout the trial lifecycle, reducing startup time, accelerating amendments, eliminating duplicate entry, and improving operational visibility across all trial functions.
Overview
Clinical trials today rarely operate within a single system. Study teams work across Electronic Data Capture (EDC), Randomization and Trial Supply Management (RTSM), ePRO platforms, CTMS environments, safety systems, analytics tools, and document repositories throughout the trial lifecycle. While these technologies support different operational functions, the workflows between them often remain disconnected.
A protocol amendment, for example, may require updates across visit schedules, randomization workflows, patient-facing systems, supply planning, and downstream reporting structures. In many organizations, these changes still rely on manual coordination between teams and systems. The result is not always a lack of technology, but it is the operational friction that is created between technologies.
This challenge is showing a growing interest in integrated eClinical platforms that support connected clinical trial workflows.
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