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Scientific method / Electronic Common Technical Document / International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use / Clinical trial / Adverse event / Common Technical Document / Institutional review board / Electronic Entertainment Expo / Communications protocol / Clinical research / Research / Science


Microsoft Word - E3 Q&As_R1_ Step4.docx
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Document Date: 2012-07-17 04:51:43

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File Size: 139,34 KB

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