The eClinical Forum offers 2 system assessment forms for investigator sites, sponsors, CROs, and regulators to use free of charge, to evaluate the suitability of an investigator site system to provide data/records for clinical trials. They are:

  • e-Source-Readiness Assessment (eSRA)
  • e-Investigator Site File System Assessment (ISF Assessment)

The 2 system assessment forms contain questions based on regulations and guidelines from global regulatory agencies for clinical research.  Since 2016, eSRA has been globally in use and regulators have accepted its inclusion in study materials. In 2024, the The ISF Assessment, based on eSRA, was released on the request of our eSRA users.  The eCF intends to publish an update to these materials annually, in Q1, to keep current with regulations and guidelines.

  • Each assessment form is packaged in a handbook providing guidance to sites on how to complete the form. The form should not be separated from the handbook, except after completion. 
  • The document “Implementing eSRA – Sponsor Assessment”, while written for eSRA, applies equally to implementing the ISF Assessment.
  • A joint document, “Regulatory documents used as a basis for the eClinical Forum eSRA and ISF Assessments” shows the correlation between these 2 assessment tools and the underlying regulatory documents.

Notice to those intending to include eCF Site System Assessment Forms in their own materials/applications: the forms are copyrighted by the eClinical Forum in 2024The eClinical Forum keeps all rights of this material. Please see the License for Fair Use in the Handbooks and “Implementing eSRA” Guide. We welcome our assessment forms to be used in other formats, however, it is required that all question text be used exactly, that all questions are included, that your use is updated when the eCF forms are updated (annually, Q1), and that eClinical Forum is notified in writing and credited. By using these materials, you acknowledge the terms and conditions for use.  The eClinical Forum is only responsible for materials as distributed via the eClinical Forum website. If using the eCF form, downloaded from this website in its original format, there is no need to notify eCF.

 

Stay Current!!

As new regulations are released or updated, the eClinical Forum will evaluate if the site system assessment form questions should be updated. To be notified of future releases of eSRA and ISF Assessment and/or to provide feedback to the team, please send an email to eSRA@eClinicalForum.org or  ISFA@eClinicalForum.org.  Your email address will not be used for purposes other than to inform you of updates to eSRA and ISF Assessment.

Do we keep a list of sites that have completed eCF Site Assessments?

We have frequently been asked if we can provide a list of which sites have already completed an eSRA. Due to privacy laws in different countries, eClinical Forum does not keep such a list. We supply the site system assessment questionnaires (eSRA and ISF Assessment), free of charge, to anyone who wants to use it. We encourage sponsors to keep a list for themselves of which sites they have received a completed assessment from. We encourage sites to store their completed eSRA or ISF Assessment in a central location (such as their IT department) so that other groups within the same organization / using the same computerised system, can use the previously completed assessment as a starting point.

eCF Site System Assessment Resources – Scroll to see all resources

eCF Overview slides -- available for your use to promote eCF participation in your company!

Sometimes, one part of an organisation takes out an eCF membership ... but other departments that could also benefit are not aware that they too could have free access to the eCF online offerings, project teams, webinars, etc. This set of slides gives an overview of the many eCF benefits available to ANYONE from a member company. Slides are current as of Dec '23. For more information, please contact your facilitator (EU: wolfgang.summa@eclinicalforum.org, NA: suzanne.bishop@eclinicalforum.org, AP: sean.higashio@eclinicalforum.org.)

27 April 2024 0
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Interested in a presenting a Technology Showcase?

The eCF Technology Showcases allow our vendor members to open dialogue with our members about their products and services. While the eCF is "non-commercial" and we do not promote any particular technology solutions, our members have asked to see what their eCF colleagues are working on.  These are one-hour webinars and can be set up anytime. Please download the information below, and then contact Suzanne Bishop for more information or to get started setting one up! (suzanne.bishop@eclinicalforum.org)

27 April 2024 0
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Interested in hosting an eCF Workshop? We come to you! It is "win-win"!

As we are not-for-profit, and keep our budget very tight, we rely on eCF member companies to host our in-person workshops. The host can help set the agenda topics and have additional seats ... as well as avoiding travel costs for those participating who are local to their site.  Please read our "Hosting Considterations" document (download below) and we are happy to have an informal conversation with you to answer any questions! Wolfgang Summa (EU workshops... wolfgang.summa@eclinicalforum.org), Suzanne Bishop (US workshops...suzanne.bishop@eclinicalforum.org), Sean Higashio (Asia workshops...sean.higashio@eclinicalforum.org). Thanks for considering!!

27 April 2024 0
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MR2023.3 of the "eCF Requirements" includes mappings to the EMA Guideline on Computerised Systems and Electronic Data in Clinical Research and is available to eCF members only

MR2023.3 of the "eCF Requirements" includes mappings to the EMA Guideline on Computerised Systems and Electronic Data in Clinical Research and is available to eCF members only

The eClinical Forum REG Team has completed a significant update to the Members-Only 2023 release of the eCF Requirements for Electronic Data for Regulated Clinical Trials (commonly referred to as the “eCF Requirements”).  This updated release incorporates extensive review and mapping of the EMA Guideline for Computerised Systems and Electronic Data in Clinical Research. This document is invaluable in determining if electronic records and systems are appropriate for use in regulated clinical trials.

24 November 2023 0
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Congratulations to our Founder, Richard Perkins, on his retirement!!!

Congratulations to our Founder, Richard Perkins, on his retirement!!!

After 23 years, Richard Perkins, our founder and chairman is retiring from eClinical Forum. We are so grateful for all of Richard’s guidance over the years, growing the eCF from a workshop with 13 participants in Nov 1999 to now a global organization with over 2300 active participants from 50 member companies (most member companies participating from several regions around the globe) and 10 global project teams. Richard will remain as a behind-the-scenes consultant during a transition period for the rest of 2023.

We had great fun toasting Richard and telling stories at both Blue Bell and Darmstadt workshops. Thanks you Richard for all you have done for us!! We will certainly miss you!!

1 July 2023 0
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