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Pharmaceutical industry / Medical research / Pharmacology / Clinical research / Pharmaceutical sciences / Pharmaceuticals policy / Marketing authorization / Validation / Bioequivalence / European Medicines Agency
Date: 2015-11-16 09:50:36
Pharmaceutical industry
Medical research
Pharmacology
Clinical research
Pharmaceutical sciences
Pharmaceuticals policy
Marketing authorization
Validation
Bioequivalence
European Medicines Agency

EMEA/CMDvCMDv/GUI/014 GUIDANCE for The Processing of Generic Applications Through MRP / DCP

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