Clinical trials are shifting from paper-based workflows to digital-first processes—but not every site is prepared to capture source data electronically. This checklist outlines 9 essential indicators of eSource-readiness, helping sponsors, CROs, and research sites assess whether their systems are ready for faster, more accurate data capture.
From structured medication and lab data to FHIR interoperability and standardized coding, the checklist highlights practical steps to evaluate your site’s infrastructure and data flows. By identifying gaps early, organizations can reduce transcription errors, cut costs, and accelerate study timelines.
Download the checklist to see how Archer helps sites transition smoothly to automated EHR-to-EDC data transfer, ensuring secure, regulatory-grade eSource adoption.