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.

 

NEWS FROM THE ECF

Success! eClinical Forum 2020 Spring Meetings replaced with Virtual Global Workshop 11-13 May 2020

  • 11/05/2020 - 14/05/2020
  • Author: Webmaster1
  • Number of views: 5075
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Success! eClinical Forum 2020 Spring Meetings replaced with Virtual Global Workshop 11-13 May 2020

The Virtual Workshop on May 11-13 that replaced the planned face-to-face Spring Workshops in Helsinki, Finland and Princeton, NJ was a huge success.  It was attended by over 130 members from around the globe, representing 46 member companies -- many of whom would not have been able to attend a face-to-face meeting and this was their first eCF workshop. 4 EMA inspectors and several guests also attended. Evaluations gave the workshop a 4.3/5.0 which is lower than our face-to-face workshops, but for our first virtual workshop we are happy with this grade!  A few comments from the evaluations: "Always an excellent group with many real experts.  The interactions are very good."  "Congratulations on an excellent event.  Everything worked well.  Sure, we missed the networking and evening events, but this worked well."  "eClinical Forum is a fantastic source of information about the landscape of eClinical today."  "eCF continues to be incredible value for money"

We are planning for another Virtual Workshop in Autumn 2020 (the week of October 12-16) and hoping to return to face-to-face workshops for Spring 2021. We now have a lot of good ideas for improvements for our 2nd Virtual Workshop! If anyone wants to make suggestions, please send to info@eclinicalforum.org. Thanks!!

eCF Requirements for Electronic Data for Regulated Clinical Trials V2019PR

  • 12 March 2020
  • Author: Webmaster1
  • Number of views: 2094
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eCF Requirements for Electronic Data for Regulated Clinical Trials  V2019PR

The eClinical Forum is happy to announce the Public release of the “eCF Requirements V2019PR” The eClinical Forum has produced a set of Requirements, which are based upon statements in regulatory documents that pertain to the design, development, implementation, and management of electronic systems that support clinical research data as well as those statements that pertain to the handling of data that will be used in a regulated clinical trial.

2020 is our 20th Anniversary Year!

  • 12 December 2019
  • Author: Webmaster1
  • Number of views: 4193
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2020 is our 20th Anniversary Year!

A lot has happened in electronic support for clinical research in the last 20 years ... and eClinical Forum has been there discussing it all!  We are pleased to be celebrating our 20th anniversary year, stronger than ever with 45+ member companies (and growing), meetings on 3 continents, global webinars that have been attended by members in over 25 countries, very active project teams, meetings with regulators, and freely adding to the knowledge base of the industry. Any organization working in this space is welcome to join. Please see the membership tab on our website (www.eclinicalforum.org) or contact us for more information!  info@eclinicalforum.org

eConsent

Evaluating the currently available data on the implementation of Electronic Consent

  • 17 October 2019
  • Author: Webmaster1
  • Number of views: 3433
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eConsent

Evaluating the currently available data on the implementation of Electronic Consent

Requirements for Electronic Data for Regulated Clinical Trials V2018PR

  • 29 March 2019
  • Author: Webmaster1
  • Number of views: 1771
  • 0 Comments
Requirements for Electronic Data for Regulated Clinical Trials V2018PR

The eClinical Forum is happy to announce the Public release of the “eCF Requirements V2018PR”. This is a project the eCF REG team has been working on for a long time and is excited to now be sharing.  

ABOUT THE ECF REQUIREMENTS:  The eClinical Forum has produced a set of Requirements, which are based upon statements in regulatory documents that pertain to the design, development, implementation, and management of electronic systems that support clinical research data as well as those statements that pertain to the handling of data that will be used in a regulated clinical trial. 

eClinical Forum Europe Meeting in Brussels, Belgium 15-17 May 2019

Better Together

  • 15/05/2019 - 18/05/2019
  • Author: Webmaster1
  • Number of views: 4208
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eClinical Forum Europe Meeting in Brussels, Belgium 15-17 May 2019

Our European meeting of the eClinical Forum took place in Brussels 15-17 May 2019, kindly hosted by Janssen.  The rousing meeting was well attended by members from Actelion, Bayer, Boehringer-Ingelheim, Bristol-Myers Squibb, CRF Bracket, CSL Behring, Eli Lilly, eResearch Technology, Glaxo SmithKline, Idorsia, Janssen Pharmaceuticals, Medidata, Merck KGaA, Munich Technical University, Neptunus Data, Novartis, Novo Nordisk, Oracle, Orion, Servier, Wega Informatik, ZeinCRO ... and guests Association for Innovative Medicines, ECRIN, and European Patients' Forum.  Meeting participants rated this meeting highly successful once again!

Audit Trail Review

  • 29 January 2019
  • Author: Webmaster1
  • Number of views: 3431
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Audit Trail Review

Best practices for meeting regulatory expectations for Audit Trail Review

Archiving and Decommissioning

Developing a position paper from the industry on the electronic archiving of study data and related topics

  • 29 January 2019
  • Author: Webmaster1
  • Number of views: 3041
  • 0 Comments
Archiving and Decommissioning

Developing a position paper from the industry on the electronic archiving of study data and related topics

CANCELED: eClinical Forum Europe Meeting in Helsinki, Finland

27-29 April 2020

  • 1 January 2019
  • Author: Webmaster1
  • Number of views: 3162
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CANCELED: eClinical Forum Europe Meeting in Helsinki, Finland

This meeting is being replaced with a Virtual Global Workshop on 11-13 May 2020.

Networking with peers has never been more important in order to stay current, collaborate on shared challenges and influence the future. The eClinical Forum offers a unique, non-commercial networking environment to learn, exchange information and ideas, collaborate on shared initiatives.

For more information on our Virtual Global Workshop, please contact info@eclinicalforum.org.

Trial of the Future

  • 1 May 2018
  • Author: Webmaster1
  • Number of views: 2754
  • 0 Comments
Trial of the Future

Evaluating emerging technologies and processes and their impact on the future of clinical trials

eSRA Maintenance

Self-Evaluating the GCP Compliance of Systems Holding Source Data

  • 1 March 2018
  • Author: Webmaster1
  • Number of views: 3035
  • 0 Comments
eSRA Maintenance

Maintaining the free eSRA (eSource-Readiness Assessment) questionnaire used by sites to self-evaluate electronic systems originating or managing data for clinical research.

eCF Autumn 2018 Meeting Dates and Locations Announced

  • 20 February 2018
  • Author: Webmaster1
  • Number of views: 12402
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eCF Autumn 2018 Meeting Dates and Locations Announced

North America: Oct 2-4 in Philadelphia, Pennsylvania USA hosted by CRF Health

Europe: Oct 23-25 in Paris, France hosted by Servier

Asia Pacific: Nov 5-6 in Tokyo Japan

Agendas will be decided a few months prior. For more information or to suggest agenda topics, please contact info@eclinicalforum.org

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eCF Views & News

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.

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eCF Birds-of-a-Feather Webinar:  EHR-EDC Integration – Implementation Overview and Learnings

eCF Birds-of-a-Feather Webinar:  EHR-EDC Integration – Implementation Overview and Learnings

Implementing EHR-EDC integrations is an emerging area of focus in the pharma industry.  This presentation will share an overview of implementing an EHR-EDC integration on 2 studies and the associated lessons learned.   Following this overview will be a group discussion on such integrations and prospects for broader adoption within our clinical trials. 

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eCF Requirements for Electronic Data for Regulated Clinical Trials PR2023

eCF Requirements for Electronic Data for Regulated Clinical Trials PR2023

The eClinical Forum is happy to announce the Public release of the "eCF Requirements for Electronic Data for Regulated Clinical Trials PR2023"

ABOUT THE ECF REQUIREMENTS:  The eClinical Forum has produced a set of Requirements, which are based upon statements in regulatory documents that pertain to the design, development, implementation, and management of electronic systems that support clinical research data as well as those statements that pertain to the handling of data that will be used in a regulated clinical trial.  We have reviewed regulatory documents from the FDA, EMA, PMDA, NMPA, MHRA and ICH to produce this set of requirements. Each Requirement has as its basis one or more statements from one or more of these regulatory documents. The Requirements can be used to determine if systems, that source or manage 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.

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