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  • Tokyo 3-4 December 2019
    Tokyo 3-4 December 2019
  • Zurich 28-30 October 2019
    Zurich 28-30 October 2019
  • Peapack 14-16 October 2019
    Peapack 14-16 October 2019
  • Brussels 15-17 May 2019
    Brussels 15-17 May 2019
  • Danbury 8-10 April 2019
    Danbury 8-10 April 2019
  • Tokyo 5-6 November 2018
    Tokyo 5-6 November 2018
  • Paris, France 23-25 October 2018
    Paris, France 23-25 October 2018
  • Philadelphia, USA 2-4 October 2018
    Philadelphia, USA 2-4 October 2018
  • Princeton 1-3 May 2018
    Princeton 1-3 May 2018
  • Darmstadt, 15-17 May 2018
    Darmstadt, 15-17 May 2018

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

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WORKING GROUPS

LEVERAGING KNOWLEDGE - DRIVING PERFORMANCE - DESIGNING THE FUTURE

eClinical Forum Project Teams work extensively with industry, healthcare organisations, academia regulators to link global stakeholders and to facilitate the development of the environment for electronic clinical research.

 

Webinar on ICH E6 Release2 (GCP) 11Jan17 - An Excellent Event
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  • Article rating: 5.0

Webinar on ICH E6 Release2 (GCP) 11Jan17 - An Excellent Event

Event Feedback

We had a fabulous level of participation with well over 140 members online from California to Japan participating in our first webinar of 2017 on the release of the addendum to E6 (Good Clinical Practice), 20 years after its original publication. Some good discussion helped us to understand the changes, opportunities and challenges. Expand the article to read more about the event.
FDA and OHRP Issue Final Guidance on the Use of Electronic Informed Consent 12/15/2016
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  • Article rating: 5.0

FDA and OHRP Issue Final Guidance on the Use of Electronic Informed Consent 12/15/2016

Re-Posted from eCF LinkedIn Group

The FDA and OHRP published final guidance aimed at providing answers to commonly asked questions about using electronic systems and processes that may employ multiple electronic media to obtain informed consent. Expand the article to read more

EDC Hosting Team Releases Final Documents
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  • Article rating: 5.0

EDC Hosting Team Releases Final Documents

Documents Available

The eCF EDC Hosting Team has released the final White Paper documenting best practices for establishing controls and operational procedures that facilitate compliance with evolving regulatory expectations for Electronic Data Capture in Clinical Trials using Service Providers. Expand the article to read more and to access the documents.
Netherlands initiative to assess electronic health record systems using eCF eSRA tool
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  • Article rating: No rating

Netherlands initiative to assess electronic health record systems using eCF eSRA tool

Partnering for Success

The Dutch Clinical Trial Foundation (DCTF) evaluate the use of eSRA for the validation of electronic health record (EHR) systems used at clinical research sites within the Netherlands. The group consists of representatives from several pharmaceutical companies, CROs and hospitals. Expand the article to learn more...

eCF Releases Key Documents and Tools
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eCF Releases Key Documents and Tools

Partnering for Success

The eCF is releasing 3 documents via the eCF website “Members” area (un/pw required).  Please feel free to download them and share with other members of your company.
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eCF Birds-of-a-Feather Webinar: Use of eCOA Metadata to Detect Fraud, Develop Risk Indices and More

Electronic solutions for patient-reported and clinician-reported outcomes provide rich metadata that can be mined for additional insights describing trial performance and driving risk-based monitoring. We will explore the use of this eCOA meta data in fraud detection, and other analytics insights and how these data might translate to risk indices to inform risk-based monitoring activities.

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