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Clinical research / Clinical data management / Electronic common technical document / Pharmaceutical industry / Pharmaceuticals policy / Common Technical Document / Marketing authorization / Electronic submission / Drug Master File


Practical Guidance For the Paper Submission of Regulatory Information in Support of a Marketing Authorisation Application When Using an eCTD or a NeeS as the Source Submission. v2.0
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Document Date: 2016-08-19 03:14:51


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File Size: 419,85 KB

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