"This is the best use of my time to remain current with what is going on in the industry."
WHO WE ARE
The eClinical Forum is a global network of peers. It provides a non‐competitive environment for innovation, learning and collaboration in clinical research.
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.)
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)
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!!
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.
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!!
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Requirements for Electronic Data for Regulated Clinical Trials - "eCF Requirements" past public releases 2018 - 2023
The eCF REG team puts out a yearly version of the "eCF Requirements" which many orgainizations use to check compliance of their systems against regulatory authority document statements. The previous versions have been requested in order to easily check the requirements that were in place in a particular year.
eCF APAC Autumn Workshop 2024 Announced
Registration is open! Our APAC Autumn workshop will be kindly hosted by Clario at the Hyatt Regency Tokyo Bayin Urayasu, Japan on November 11-12 2024.
eCF Birds-of-a-Feather Round-Table: Risk-Based Source Data Verification
This topic is coming out of a discussion that started at the eCF Workshop in Massachusetts in October. The group decided they wanted more time to delve more deeply into this discussion and to include eCF members from other regions. The discussion will be around:
eCF “Think GCP” Webinar: ICH E6(R3) for eCF Members
Presenter: Rebecca Stanbrook, GCP Strategic Lead, Process & Risk Surveillance, Novartis, EFPIA Topic Lead ICH E6(R3)
About this topic: The final piece of the GCP renovation puzzle, revision 3 of ICH GCP. Understand the background to the renovation, key changes and the philosophy of the changes in this one hour webinar.