eISF Overview

Trial Interactive electronic Investigative Site File (eISF) solution reduces administration loads and improves speed and compliance for site personnel, CRAs, and study teams. Digital investigative site binder processes maintain certified copies of source file documentation and essential documents required for each clinical study. A seamless, connected eTMF allows for the automatic indexing of essential documents to the eTMF. The ability to conduct remote site monitoring, recommended by the FDA and EMA, helps CRAs work more efficiently in today’s increasingly virtual environment while reducing travel expenses.