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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
Date: 2016-08-19 03:16:02
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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Source URL: esubmission.ema.europa.eu

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