The DPHARM conference brings together senior clinical operations executives and thought leaders to explore innovations in modernizing clinical trials, patient-centric design, and partnerships across the trial ecosystem. CRIO will be at DPHARM 2026, connect with our team to learn how our eSource and workflow solutions are accelerating trial delivery.
Please join us for the following session featuring Ken Getz from the Tufts Center for the Study of Drug Development.
Date: Tuesday, September 15
Time: 12:35PM to 12:45PM
Session Title: Examining the Source Document Preparation Process During Study Start-up
Session Description: Study start-up timelines have been increasing at a rapid rate. This session looks at underlying factors contributing to longer start-up durations and presents new data on how sites translate clinical trial protocols and related information into template source documents, study plans and support materials. Based on a survey conducted in late 2025 by Tufts CSDD and CRIO, this presentation highlights key study insights including a comprehensive mapping of systems and workflows that global investigative sites use to capture, manage and transmit clinical research data. The session will also discuss the implications of the results and opportunities and solutions to improve start-up efficiency, speed and quality.
