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 ForumThe 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 15 June 2026

Webinar "AI Validation"

eCF June Webinar

Event date: 24/06/2026 15:00 - 16:00 Export event

Are you interested in AI Validation? Join our webinar on June 24th 2026 

As generative and agentic AI become part of pharmaceutical operations, how do we validate these systems in a practical way? Generative and agentic AI are already in clinical trial operations, but the validation rulebook hasn't kept up. CSV and CSA were built for software that behaves predictably, not for systems that produce novel outputs and act before anyone reviews them. "Human in the loop" isn't a validation strategy: the April 2, 2026 FDA warning letter on AI over-reliance showed human review can be present and still fail.

Join us on Wednesday, June 24th for a webinar exploring the future of validating AI-enabled software. The session will identify key challenges, discuss practical, risk-based approaches, and talk about next steps. Our goal is to bring together cross-industry experts in an ongoing working group to build one practical, risk-based framework. If you're interested in contributing your expertise and helping shape the discussion, join the webinar on June 24th 2026, 10am EDT

A registration link was sent out in this month's newsletter. If you haven't received it and are interested in participating, write jana.summa@eclinicalforum.org 

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Author: Jana Summa

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