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  • Princeton 1-3 May 2018
    Princeton 1-3 May 2018
  • Darmstadt, 15-17 May 2018
    Darmstadt, 15-17 May 2018
  • Tokyo 4-5 December 2017
    Tokyo 4-5 December 2017
  • Wellesely, MA 16-18 October 2017
    Wellesely, MA 16-18 October 2017
  • BERLIN 26-28 SEP 2017
    BERLIN 26-28 SEP 2017
  • REYKJAVIK 8-10 MAY 2017
    REYKJAVIK 8-10 MAY 2017
  • BLUE BELL, PA 24-26 OCT 2016
    BLUE BELL, PA 24-26 OCT 2016
  • BASEL 10-12 OCT 2016
    BASEL 10-12 OCT 2016
  • SINGAPORE 1-3 JUNE 2016
    SINGAPORE 1-3 JUNE 2016
  • UPPSALA 17-19 MAY 2016
    UPPSALA 17-19 MAY 2016
  • INDIANAPOLIS 25-27 APR 2016
    INDIANAPOLIS 25-27 APR 2016
  • NEW YORK 19-21 OCT 2015
    NEW YORK 19-21 OCT 2015
  • HORSHAM 5-7 OCT 2015
    HORSHAM 5-7 OCT 2015
  • SINGAPORE 3-4 SEP 2015
    SINGAPORE 3-4 SEP 2015
  • NORTH WALES, PA 18-20 MAY 2015
    NORTH WALES, PA 18-20 MAY 2015
  • SIENA 28-30 APR 2015
    SIENA 28-30 APR 2015
  • BANGALORE 5-6 FEB 2015
    BANGALORE 5-6 FEB 2015
  • CAMBRIDGE, MA 22-24 OCT 2014
    CAMBRIDGE, MA 22-24 OCT 2014
  • COPENHAGEN 16-18 SEP 2014
    COPENHAGEN 16-18 SEP 2014
  • SINGAPORE 20-21 MAY 2014
    SINGAPORE 20-21 MAY 2014
  • AMSTERDAM 14-16 MAY 2014
    AMSTERDAM 14-16 MAY 2014
  • BOULDER 30 APR - 2 MAY 2014
    BOULDER 30 APR - 2 MAY 2014
  • RESTON, VA 28-30 OCT 2013
    RESTON, VA 28-30 OCT 2013
  • DUBLIN 18-20 SEP 2013
    DUBLIN 18-20 SEP 2013
  • KASNSAS CITY 7-9 MAY 2013
    KASNSAS CITY 7-9 MAY 2013
  • EDINBURGH 22-24 APR 2013
    EDINBURGH 22-24 APR 2013
  • MONTVILLE, NJ 14-16 NOV 2012
    MONTVILLE, NJ 14-16 NOV 2012
  • MADRID 1-3 OCT 2012
    MADRID 1-3 OCT 2012
  • PARIS 21-23 MAY 2012
    PARIS 21-23 MAY 2012
  • EAST HANOVER, NJ 7-8 MAY 2012
    EAST HANOVER, NJ 7-8 MAY 2012
  • STRASBOURG 28-30 NOV 2011
    STRASBOURG 28-30 NOV 2011
  • NEWPORT BEACH 2-3 NOV 2011
    NEWPORT BEACH 2-3 NOV 2011
  • BANBURY 4-6 MAY 2011
    BANBURY 4-6 MAY 2011
  • CAMBRIDGE, MA 12-13 APRIL 2011
    CAMBRIDGE, MA 12-13 APRIL 2011
  • FORT LAUDERDALE 3-5 NOV 2010
    FORT LAUDERDALE 3-5 NOV 2010
  • BRUSSELS 6-8 OCT 2010
    BRUSSELS 6-8 OCT 2010
  • PARIS 5-7 MAY 2010
    PARIS 5-7 MAY 2010

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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Regulatory

BoF Webinar: Requirements for Electronic Data for Regulated Clinical Trials (eCF Requirements)
  • 552
  • Article rating: 5.0

BoF Webinar: Requirements for Electronic Data for Regulated Clinical Trials (eCF Requirements)

Offered twice: March 27 2018 at UTC 1500 and April 17 2018 at UTC 0800

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

We will hold 2 webinars to introduce the “eCF Requirements” such that we can accommodate member’s time zones around the globe as well as upcoming national holidays.

BoF Webinar: Requirements for Electronic Data for Regulated Clinical Trials (eCF Requirements)
  • 552
  • Article rating: 5.0

BoF Webinar: Requirements for Electronic Data for Regulated Clinical Trials (eCF Requirements)

Offered twice: March 27 2018 at UTC 1500 and April 17 2018 at UTC 0800

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

We will hold 2 webinars to introduce the “eCF Requirements” such that we can accommodate member’s time zones around the globe as well as upcoming national holidays.

ECF REPRESENTATIVES MEET WITH EMA GCP IWG
  • 3200
  • Article rating: 5.0

ECF REPRESENTATIVES MEET WITH EMA GCP IWG

Meeting With Interested Parties On Topics Related To E-Source Data/ EDC Tools In Clinical Trials

Representatives from the eClinical Forum participated in the meeting with inspectors and observers in London 12th June to discuss challenges and trends in Clinical Research. We presented the work of the eClinical Forum in the areas of contractual requirements and risk-based software validation…  Expand article to read more...

Webinar on ICH E6 Release2 (GCP) 11Jan17 - An Excellent Event
  • 5740
  • 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
  • 6614
  • 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

Free access to GCDMP
  • 5633
  • Article rating: No rating

Free access to GCDMP

Re-Post from eCF LinkedIn

Anyone can now access to this important document for Data Management and Clinical Research.
Netherlands initiative to assess electronic health record systems using eCF eSRA tool
  • 6632
  • 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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  • Article rating: No rating

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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«April 2018»
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3/27/2018 UTC
53

BoF Webinar: Requirements for Electronic Data for Regulated Clinical Trials (eCF Requirements)

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

We will hold 2 webinars to introduce the “eCF Requirements” such that we can accommodate member’s time zones around the globe as well as upcoming national holidays.

Read more
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1617
4/17/2018 UTC
53

BoF Webinar: Requirements for Electronic Data for Regulated Clinical Trials (eCF Requirements)

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

We will hold 2 webinars to introduce the “eCF Requirements” such that we can accommodate member’s time zones around the globe as well as upcoming national holidays.

Read more
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5/1/2018 - 5/3/2018 UTC
43

North America Spring Meeting May 1-3 2018 -- Agenda

This meeting is open to industry, healthcare, academic and government partners who are members of the eClinical Forum. Please contact  info@eclinicalforum.org to discuss membership options. Click on title to download Preliminary Agenda.

 

Read more
2
5/1/2018 - 5/3/2018 UTC
43

North America Spring Meeting May 1-3 2018 -- Agenda

This meeting is open to industry, healthcare, academic and government partners who are members of the eClinical Forum. Please contact  info@eclinicalforum.org to discuss membership options. Click on title to download Preliminary Agenda.

 

Read more
3
5/1/2018 - 5/3/2018 UTC
43

North America Spring Meeting May 1-3 2018 -- Agenda

This meeting is open to industry, healthcare, academic and government partners who are members of the eClinical Forum. Please contact  info@eclinicalforum.org to discuss membership options. Click on title to download Preliminary Agenda.

 

Read more
456

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