Clinical Site Alliance
Overview
There is a significant gap in the efficiency and accessibility of EFS in the industry, where the time and complexity of patient enrollment, trial initiation, and site coordination often delay access to innovative medical devices. The Clinical Site Alliance addresses these challenges by bringing together experienced sites in a collaborative network to enhance and standardize enrollment processes.
Objective
To establish a collaborative network of experienced sites to reduce enrollment time and provide “First-in-World” access for U.S. patients to innovative medical devices and therapies.
Get Involved
The EFS Clinical Site Alliance aims to unite clinical sites demonstrating expertise in conducting EFS studies. This initiative seeks to enhance the performance of EFS in the United States by facilitating the sharing of best practices and operational insights. The Clinical Site Alliance will customize and improve previously developed tools to support this effort.
Accelerate EFS Toolkit
MDIC’s work within the EFS program includes tracking EFS performance metrics, and developing tools and best practices for EFS sponsors and clinical researchers alike. In combination, these efforts are anticipated to drive overall EFS efficiency and support continuous assessment of EFS efficiency and effectiveness for US patients.
