Author:
Bilbault Pascal,Belorgey Chantal,Zannad Faiez,Golinelli Danielle,Pletan Yannick,Abiteboul Michel,Bertram Delphine,Cornu Catherine,Chassany Olivier,Demotes-Mainard Jacques,Demarez Jean-Paul,Diebolt Vincent,Dubray Claude,Ericson Mats,Orvoen Elisabeth Frija,Hirsch François,Juillet Yves,Lamarque Véronique,Le Coent Rémi,Libersa Christian,Marey Christine,Marchenay Brigitte,Mijonnet Armelle,Plattner Valérie,Raison Anne,Rossignol Patrick,Rusch Philippe,Simon Tabassome
Reference12 articles.
1. Submission of clinical studies to Ethics Committees or clinical trials registers – the authors’ point of view;Pehboeck;Intensive Care Med,2009
2. Conference on the Impact on Clinical Research of European Legislation (FP7 program, ICREL), results § discussion, Brussels;European Forum for Good Clinical Practice (EFGCP),2008
3. Common definition for categories of clinical research: a prerequisite for a survey on regulatory requirements by the European Clinical Research Infrastructures Network (ECRIN);Kubiak;Trials,2009
4. Projet de Loi sur les recherches sur la personne;Jardé,2009
5. CTA assessment in member states;Clinical Trials Facilitation Group,2008
Cited by
6 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献