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Clinical research / Clinical data management / Pharmaceutical industry / Electronic common technical document / Pharmaceuticals policy / Common Technical Document / Marketing authorization / ASMF / European Medicines Agency / European Directorate for the Quality of Medicines / Dossier / Electronic submission


Revision version 1.5 for public consultation Comments byJune 2016
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Document Date: 2016-08-19 03:14:57

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File Size: 471,00 KB

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