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Pharmaceuticals policy / Pharmaceutical industry / Clinical research / Drug safety / Healthcare quality / Bioequivalence / Summary of Product Characteristics / Marketing authorization / Test data exclusivity / Pharmacovigilance / Supplementary protection certificate / European Medicines Agency


CMDh QUESTIONS & ANSWERS GENERIC APPLICATIONS Doc. Ref.: CMDh, Rev.1 AprilSUBMISSION OF A DESCRIPTION OF PHARMACOVIGILANCE SYSTEM AND EU RISK
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Document Date: 2016-05-16 05:10:10


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