Manual transcription of patient records into EDC systems carries a pooled error rate above 6.5% when abstracted from medical records, according to a systematic review of 93 clinical research papers, and fixing those errors downstream consumes a disproportionate share of CRA monitoring time. That cost is exactly what CRScube and Mednet are targeting with a webinar on October 14, 2026, at 11 a.m. ET, where they will demonstrate an integration-free EHR-to-EDC capability built into the cubeCDMS platform.

The distinction worth watching is the word “integration-free.” Conventional EHR-to-EDC connections require site-level technical agreements, IT authorization workflows, and implementation work that many smaller sites simply cannot absorb. That friction has kept a large share of the roughly $1.84 billion global EDC market reliant on manual re-entry despite the existence of automated alternatives. CRScube, which acquired Mednet in November 2025 to extend its North American footprint, is positioning this feature as something sponsors and CROs can deploy across sites without triggering those technical hurdles on either end.

The session will include a live demonstration showing site staff capturing data directly inside cubeCDMS without re-keying from a separate EHR screen. The claim is that eliminating transcription at the point of capture also compresses the source data verification cycle, since records don’t need to be cross-checked against a manual entry that may already contain an error. The FDA’s October 2024 guidance on electronic records and signatures in clinical investigations clarified expectations around audit trails and data integrity for systems like these, giving vendors a clearer compliance target and giving sponsors more confidence to deploy EHR-connected tools broadly.

The concrete test for this approach is whether query rates at sites using the tool actually fall in sponsored trials. If CRScube shares any internal query-reduction figures during the live demo, that number is the one worth benchmarking against your current site performance data.

Source link: https://www.mednetsolutions.com/webinars/webinar-streamlining-clinical-data-flow-with-integration-free-ehr-to-edc/

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Moe Alsumidaie, MBA, MSF, is founder and Chief Editor of Vanguard Publications, which publishes Clinical Trial Vanguard, Pharma Vanguard and BullScope, and Head of Research at CliniBiz. He has two decades in clinical trial operations and data science, with earlier roles at Genentech, Abbott Vascular and Stanford University Medical Center, and is a guest lecturer in clinical trial sciences at Rutgers University.