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Clinical research / Clinical data management / Pharmaceutical industry / Electronic common technical document / Pharmaceuticals policy / Marketing authorization / Common Technical Document / Validation / Product lifecycle


22 JulyJuly 2016 EMAv7.0 User Guidance for Marketing Authorisation Holders (MAHs) for PSUR Repository
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Document Date: 2016-08-19 03:16:02


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File Size: 874,00 KB

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