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

EU Hybrid Workshop Announced

Published on 20 August 2024

EU Hybrid Workshop Announced

Oct 15-17 2024

Event date: 15/10/2024 - 17/10/2024 Export event

Come join us for discussions on “How new and evolving technology is changing the roles in clinical research” at the eClinical Forum Hybrid Workshop, kindly hosted by Boehringer Ingelheim in Ingelheim am Rhein, Germany on October 15-17, 2024. The workshop will provide the usual updates and discussion on the eCF project teams and recent regulatory issues, as well as a day to focus on how the roles of the different participants in the clinical research path (from patient through to regulatory submission) have and will continue to change as technology evolves.

This workshop will be available for in-person and remote participation. There will be networking/social events on both evenings.  eCF Member companies can register up to 2 seats at this workshop. For those wishing to register for the US workshop  you can do so here : Oct 22-24: eCF US Workshop

2024 Autumn Workshop Topics: 

  • Regulatory updates: eCF meeting with EMA IWG
  • eCF Project Team updates and break-out discussions, including Audit Trail Review Analytics, Digital Health Technologies Governance, and Essential Metadata
  • Validation/Continuous Learning in AI products
  • Changing roles in e-clinical for: Patients, Sites, Clin-ops, Safety, Supply/logistics, Data managers, Statisticians, IT Support, Training dept, Auditors/QA, Medical Writing, Archivists.
    • We are looking for people to present their perspective on their changing role -- Please contact us!!

Workshop will take place at:

Boehringer Ingelheim:  Binger Str. 173, 55218 Ingelheim am Rheim, Germany

eCF Member companies may register up to 2 seats at this workshop by Oct 1; additional seats can be registered for a waiting list.  For more information or to register: eCF EU Hybrid Workshop Ingelheim, Germany Oct 15-17 2024 (eclinicalforum.org)

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