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

2006, Sept: The Future Vision of Electronic Health Records as eSource for Clinical Research

  • 1 October 2006
  • Author: Webmaster1
  • Number of views: 1243
  • 0 Comments
2006, Sept: The Future Vision of Electronic Health Records as eSource for Clinical Research

Please download to review this position paper.

ECF Steering Committee

  • 1 January 2006
  • Author: Webmaster1
  • Number of views: 1986
  • 0 Comments
ECF Steering Committee

Elected team providing strategic direction and governance

2005: US PhRMA's Electronic Clinical Data Capture Position Paper Revision 1

  • 1 May 2005
  • Author: Webmaster1
  • Number of views: 1259
  • 0 Comments
2005: US PhRMA's Electronic Clinical Data Capture Position Paper Revision 1

Please download to review this position paper.

2004: EDC Performance Metrics - Full Report

  • 22 June 2004
  • Author: Webmaster1
  • Number of views: 1412
  • 0 Comments
2004: EDC Performance Metrics - Full Report

The eClinical Forum's 2004 Metric Survey of companies involved in conducting EDC trials assesses the feasibility of establishing standard EDC performance metrics.

2003: eCF Presentation to EMEA GCP Inspectors on EDC

  • 22 October 2003
  • Author: Webmaster1
  • Number of views: 1342
  • 0 Comments
2003:  eCF Presentation to EMEA GCP Inspectors on EDC

Please download to review this presentation.

THE USE OF ELECTRONIC SOURCE DOCUMENTATION - V1.1 May 2003

  • 12 May 2003
  • Author: Webmaster1
  • Number of views: 2028
  • 0 Comments
THE USE OF ELECTRONIC SOURCE DOCUMENTATION - V1.1 May 2003

This 13-page position paper on eSource (source data that has been captured by an electronic tool which is a replacement for paper) describes the regulatory environment for the ultimate benefit of all stakeholders involved in EDC.

2003: Regulatory Environment for Electronic Data Capture

  • 12 February 2003
  • Author: Webmaster1
  • Number of views: 1295
  • 0 Comments
2003: Regulatory Environment for Electronic Data Capture

Please download to review this report.

2001: Cost / Benefit Analysis of EDC

  • 12 December 2001
  • Author: Webmaster1
  • Number of views: 1359
  • 0 Comments
2001: Cost / Benefit Analysis of EDC

Please download to review this report.

2001: Investigator Survey

  • 12 June 2001
  • Author: Webmaster1
  • Number of views: 2022
  • 0 Comments
2001:  Investigator Survey

The eClinical Forum has conducted a global survey of investigational site experiences and expectations with EDC. The survey covers:

* Computer use and site facilities.
* Current experience with EDC.
* Satisfaction with EDC features.
* Future expectations.

1999: Industry Survey

  • 3 January 2000
  • Author: Webmaster1
  • Number of views: 1947
  • 0 Comments
1999:  Industry Survey

A survey was undertaken by the eClinical Forum to review the pharmaceutical industry’s experience to date with Electronic Data Capture (EDC) and to better understand future trends.

The survey report incorporates the responses of 30 companies, and includes a mixture of EU and US ethical pharmaceutical and biotechnology companies representing 8 of the top 10, 12 of the top 20 and 18 of the top 40 by revenue.

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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:  Site experience in the day-and-age of hybrid e-trials

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.

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