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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.
What expectations do FDA, EMA, PMDA, MNPA, MHRA and ICH put on your e-clinical systems … and how can you easily keep an eye on them as they change? Happily for you – the eClinical Forum is releasing its 8th 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 these regulatory authorities, and boils them down into 37 statements for you to follow. Each eCF Requirement is “held up” by a series of mappings to the regulatory authority documents. The eCF Requirements can be used to determine if systems that handle data which will become part of a regulated clinical trial are consistent with regulatory requirements and if systems and process that manage these data have the necessary features.
The eClinical Forum is releasing this version (V2024 PR) as a service to the eClinical Community. The V2025, recently released, is available to eClinical Forum members only. For information on becoming an eClinical Forum member, please see our Membership tab on this website.
This is an ongoing effort of the eClinical Forum’s “Regulatory Expert Group” (REG). They have put in countless hours to ensure that this comprehensive checklist for evaluating electronic systems that will manage data used in regulated clinical research remains up-to-date against regulations and guidance from FDA /United States, EMA/European Union, PMDA/Japan, NMPA/China, MHRA/United Kingdom, TFDA/Taiwan ROC, and ICH (International Council on Harmonization) among others. This work is a result of the vast experience of the REG members who come from a variety of different eCF Member companies. They have spent hours debating each regulation or guidance and how to word the eCF Requirements to meet the needs in the regulatory documents. If any one company were to undertake such a project, the hours spent would justify an eClinical Forum membership very quickly. For this reason, the eCF Requirements V2025 is released to eClinical Forum members only, with the V2024 now being released to the public.
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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.
V2025 vs V2024 and Regulatory Basis
Comparison of V2025 to V2024 for both Form/S (eSource) and Form/F (eFile) and mapping to regulatory authority document statements
Implementing eSRA - Sponsor Perspective
This guideline provides additional information to sponsors/CROs evaluating the use of eSRA forms for their organisation.
eSRA Handbook and Assessment Forms V2025
The one file you will need to complete an assessment of your e-Source or e-File systems.
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 8th 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, TFDA and ICH , and boils them down into 37 unique statements or "eCF Requirements".
eCF Spring 2025 Workshops Announced
We are pleased to announce our 2025 Spring Workshops.
These workshops will be in-person, with the UK workshop also being live-streamed for any eCF member around the globe to join. Each eCF member organisation has a certain number of seats available for in-person participation, depending on the membership type (please contact your eCF Primary representative to discuss using a member seat). Joining the UK workshop via live-stream is gratis for anyone in an eCF member organisation.
April 8-10: Bangalore, India (kindly hosted by i2e)
April 29-May 1: King-of-Prussia, PA, USA (kindly hosted by CSL Behring)
May 13-15: Walton Oaks, Surrey, UK (kindly hosted by Pfizer)