This article has Open Peer Review reports available.
Standard requirements for GCP-compliant data management in multinational clinical trials
- Christian Ohmann†1Email author,
- Wolfgang Kuchinke†1,
- Steve Canham†2,
- Jens Lauritsen3,
- Nader Salas4,
- Carmen Schade-Brittinger5,
- Michael Wittenberg5,
- Gladys McPherson6,
- John McCourt7,
- Francois Gueyffier8,
- Andrea Lorimer9,
- Ferràn Torres10 and
- the ECRIN Working Group on Data Centres
© Ohmann et al; licensee BioMed Central Ltd. 2011
Received: 24 September 2010
Accepted: 22 March 2011
Published: 22 March 2011
Open Peer Review reports
Pre-publication versions of this article are available by contacting firstname.lastname@example.org.
|24 Sep 2010||Submitted||Original manuscript|
|13 Dec 2010||Reviewed||Reviewer Report - Roxanne Ward|
|13 Dec 2010||Reviewed||Reviewer Report - Christine Kubiak|
|11 Feb 2011||Author responded||Author comments - Christian Ohmann|
|Resubmission - Version 2|
|11 Feb 2011||Submitted||Manuscript version 2|
|Resubmission - Version 3|
|Submitted||Manuscript version 3|
|Resubmission - Version 4|
|Submitted||Manuscript version 4|
|18 Mar 2011||Author responded||Author comments - Christian Ohmann|
|Resubmission - Version 5|
|18 Mar 2011||Submitted||Manuscript version 5|
|22 Mar 2011||Editorially accepted|
|22 Mar 2011||Article published||10.1186/1745-6215-12-85|
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