Revising the ECRIN standard requirements for information technology and data management in clinical trials.

Christian Ohmann 1, * Steve Canham 1 Catherine Cornu 2 Jochen Dreß 3 François Gueyffier 4 Wolfgang Kuchinke 1 Enrico Nicolis 5 Michael Wittenberg 6
* Auteur correspondant
1 Coordination Centre for Clinical Trials
2 CIC CHU Lyon (inserm)
3 ZKS - Centre for Clinical Studies
4 Service de Pharmacologie Clinique et Essais Thérapeutiques
5 Department of Cardiovascular Research
6 Coordination Centre for Clinical Trials
Abstract : The pilot phase of the ECRIN (European Clinical Research Infrastructure Network) certification programme for European data centres, in late 2011, led to a substantial revision of the original ECRIN standards, completed by June 2012. The pilot phase, the conclusions drawn from it and the revised set of standards are described. Issues concerning the further development of standards and related material are discussed, as are the methods available to best support that development. A strategy is outlined based on short-lived specific task groups, established as necessary by a steering group drawn from ECRIN-ERIC. A final section discusses possible future developments.
Keywords : Standards Information technology Data management ECRIN European Certification
Type de document :
Article dans une revue
Trials, BioMed Central, 2013, 14 (1), pp.97. 〈10.1186/1745-6215-14-97〉
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http://www.hal.inserm.fr/inserm-00823379
Contributeur : Ed. Bmc <>
Soumis le : jeudi 16 mai 2013 - 17:16:52
Dernière modification le : lundi 19 mars 2018 - 10:04:48
Document(s) archivé(s) le : lundi 19 août 2013 - 16:36:14

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Christian Ohmann, Steve Canham, Catherine Cornu, Jochen Dreß, François Gueyffier, et al.. Revising the ECRIN standard requirements for information technology and data management in clinical trials.. Trials, BioMed Central, 2013, 14 (1), pp.97. 〈10.1186/1745-6215-14-97〉. 〈inserm-00823379〉

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