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 30 November 2016

Electronic Informed Consent Technology Showcase - An Excellent Event

Event Feedback

Untitled 2Electronic Informed Consent in clinical trials has been highlighted as a topic of interest at recent eClinical Forum meetings. The technology demonstration provided a good insight into the functional capabilities, business opportunities and challenges of eICF systems.


Our thanks go to Scott Askin, Novartis, Switzerland and to Eric Delente, DrugDev, USA who facilitated a very interesting webinar.
Slides used during the event can be downloaded by eCF members.

The session explored in detail:

  • How eICF can improve how we engage, manage and monitor patients involved in clinical trials
  • The change management challenges
  • How such Digital Technologies can make a significant difference
  • The functionality offered by one eICF system offered by Enforme Interactive/Drug Dev’s SecureConsent Application
  • Measured improvements in comprehension and process control
  • The steady growth in use and experience
  •  Best practices, business value and Regulatory acceptance
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