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Breaking down silos: why unifying EDC and endpoint adjudication accelerates clinical trials
Separate EDC and endpoint adjudication systems can create duplicate work and delay clinical event reviews. Explore how a unified approach connects data collection with independent review, reduces manual reconciliation and supports timely, reliable endpoint evaluation.
How to make sites want to take part in clinical trials with Vivienne van de Walle
The opening episode of Clinical Data Talks season 4 features Vivienne van de Walle, founder of an independent clinical site. She talks about technology burden, patient centricity, and collaboration between sponsors and sites.
The end of dual data entry: How native AI is rewriting the rules of EHR/EMR data intake
Double data entry remains a major burden for clinical trial sites, creating unnecessary work and increasing the risk of transcription errors. This article explores how native AI-powered EMR/EHR data intake in cubeCDMS can capture patient data directly from the active screen, reducing manual entry and helping sites, CRAs, data managers, and sponsors work with cleaner, more timely clinical data.
