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The eClinical Forum is a global network of peers. It provides a non‐competitive environment for innovation, learning and collaboration in clinical research.
Event date: 17/05/2022 - 19/05/2022 Export event
We are pleased to announce that registration is now open for our next Workshop at the Crowne Plaza Brussels Airport, Brussels on 17-19 May 2022.
This hybrid workshop is available for face-to-face or remote participation. Please note: not all of the sessions can be streamed for remote participation. We encourage you to participate in person if you can. For the moment, we anticipate that participation in person will require you to be fully vaccinated and with a negative Covid test.
Our recent workshops have been entirely virtual, and I know that many of us are anxious to get back to the more interactive workshops of the pre-pandemic era. Nearly everyone (91%) that took part in the short poll at the end of the last workshop in October 2021 expressed a hope for some form of face-to-face component during 2022. A hybrid meeting offers us the best of both worlds:
Of course, new variants might interfere with our planning and, if covid restrictions on travel and meeting together prevent us offering a face-to-face meeting, then the live stream sessions will run as outlined in the attached agenda.
We have an exciting agenda for the meeting and an outline is attached.
We encourage you and your colleagues to REGISTER NOW for the sessions that you would like to attend (https://eclinicalforum.org/forms/hybrid-workshop-brussels-17-19-may-2022 ). Please register your interest early for places at the face-to-face meeting as this space is limited. Space within the virtual sessions is not limited and you are welcome to participate from any region.
You may also want to consider registration for the live streamed sessions of the Americas Workshop taking place on 8-10 June 2022 using this link.
Meeting Topics:
DECENTRALISED CLINICAL TRIALS
REAL WORLD EVIDENCE & DIGITAL HEALTH TECHNOLOGIES
ELECTRONIC TRIAL MASTER FILE
INNOVATIONS IN CLINICAL RESEARCH
IN THE NEWS
Registration
This meeting is open to organisations that are members of the eClinical Forum.
About the eClinical Forum
The eClinical Forum offers a unique, non-commercial networking environment to learn, exchange information and ideas, collaborate on shared initiatives and to influence the future.
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eCF Birds-of-a-Feather Webinar: Site experience in the day-and-age of hybrid e-trials
Back by popular demand! Dr. van de Walle presented at the hybrid European eCF workshop in May … and we just ran out of time to answer all the questions! So many requests to ask Viviënne to present again with more time. So, here it is! Not to be missed! Viviënne is a full-time investigator and founder of an indepenent research site. She has vast site and patient experience and will share her insight into how hybrid trials are going for the sites and the patients.
eCF Views & News
We send out a brief monthly newsletter via email to all our active eCF members to keep them abreast of the activities of eCF that they can participate in. The more who participate, the better we are "A Network Powered by Peers". Click to see the most current newsletter.
2024 Members Release of the "Requirements for Electronic Data for Regulated Clinical Trials" (commonly referred to as the “eCF Requirements”)
The "eCF Requirements" Members Release V2024 has been released. This is a significant accomplishment by the eClinical Forum’s “Regulatory Expert Group” (REG) as they have put in countless hours over many years to be able to produce such a comprehensive list of compliance requirements for electronic systems that will manage data used in regulated clinical research, against regulations and guidances from 40 different documents from FDA, EMA, PMDA, NMPA, MHRA and ICH and ISO.
Public release of the "Requirements for Electronic Data for Regulated Clinical Trials" (commonly referred to as the “eCF Requirements”)
The eClinical Forum is releasing its 7th public version of the “eCF Requirements” which takes all of the requirements and guidance directions that pertain to electronic data and electronic systems that support clinical research, from FDA, EMA, PMDA, MNPA, MHRA and ICH , and boils them down into 37 unique statements or "eCF Requirements".
eCF Birds-of-a-Feather Webinar: Protocol Optimization using AI/ML
We will be discussing the transformative potential of Artificial Intelligence (AI) and Generative AI in clinical development.
eCF Technology Showcase Webinar: OpenClinca “Unlocking Clinical Data from EHRs”
What if site users could launch the eCRF with a single click from the patient’s chart, and automatically populate CRFs with data from the chart? This is a Technology Showcase hosted by our newest eCF member, OpenClinica.
eCF Free Public Webinar: Regulatory Requirements for Electronic Data/Systems for Clinical Trials, and associated site system assessments
The eClinical Forum is pleased to offer a free public webinar – to provide information on our 3 free tools: The “eCF Requirements” (Requirements for electronic data for regulated clinical trials), eSRA (Site eSource-Readiness Assessment), and ISF (Investigator Site File System) Assessment. 18-Sept-24: Registration Required.
eCF Americas Autumn Workshop 2024 Announced
Registration is open! Our Americas Autumn workshop will be kindly hosted by eClinical Solutions at their offices in Mansfield, Massachussetts (near Boston/Patriots Stadium) on October 22-24 2024.