The eClinical Forum offers 2 absolutely free system assessment forms that consist of regulatory-based questions for evaluating the suitability of an investigator site system to provide data/records for clinical trials.Both forms are part of the eSRA Handbook which provides guidance to sites on how to complete the forms.  We request that Sponsors and CROs do not separate the forms from the handbook. Sites may separate the forms from the handbook after completion such that they are only sharing and storing the completed forms.

Notice to those intending to include eCF Site System Assessment Forms in their own materials/applications: the forms are copyrighted by the eClinical Forum. The eClinical Forum keeps all rights of this material. Please see the License for Fair Use in the eSRA Handbook and “Implementing eSRA” Guide. By using these materials, you acknowledge the terms and conditions for use as described in the eSRA documents.  The eClinical Forum is only responsible for materials as distributed via the eClinical Forum website. If using the eCF forms downloaded from this website in original formats, there is no need to notify eCF.

Stay Current!!

eSRA materials are updated annually and released at the end of Q1. To be notified of future releases and/or to provide feedback to the team, please send an email to eSRA@eClinicalForum.org.  Your email address will not be used for purposes other than to inform you of updates to eCF Site System Assessments.

Does the eClinical Forum keep a list of sites that have completed eCF Site Assessments?

Due to privacy laws in different countries, we do not keep such a list, however sponsors can keep a list of eSRAs they have received.We encourage sites to store their completed assessments in a central location (such as their IT dept) so that other groups within the same organisation / using the same computer system, can use the previously completed assessment as a starting point.

eCF Site System Assessment Resources – Scroll to see all resources

Published on 28 October 2026

eCF Webinar November: FDA warning letters for audit trail analytics

Webinar November 2026

Event date: 10/11/2026 10:00 - 11:00 Export event

eCF Webinar November 2026: FDA warning letters are telling you what to fix. Is your audit trail analytics listening? 

FDA warning letters name what went wrong. They rarely explain what a functioning audit trail analytics program should have caught instead.
This session works through a FDA warning letter in detail and uses it as a case study, tracing the inspection finding back through the data to identify where the analytical signal existed, why it was missed, and what a fit-for-purpose audit trail review program would have detected before the letter was written.

The goal is not to teach you about the letter, but to give you a method for reading any letter as a diagnostic for your own program. Attendees leave with a structured approach for connecting FDA inspection findings to audit trail analytics design, and a clearer picture of where their current programs may have the same blind spots.

The webinar will be held on Tuesday, November 10, 2026 and will take place twice. 

You can find more information and sign up here

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Author: Jana Summa

Categories: Webinar/Telecon, Visible by Public

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