The eClinical Forum eSource Sub-team is working on a common assessment tool to determine Investigator Site eSource-Readiness. This tool has been piloted at 17 sites and presented to FDA and EMA for review. The eClinical Forum is currently planning on releasing a simple version of this tool by the end of 2013. For more information, please review this presentation which is a version of what was presented to the FDA and EMA as well as the DIA Annual meeting and the exlPharma eClinical Summit. For more information, please contact Suzanne.Bishop@eclinicalforum.org.