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Clinical research / Pharmaceutical industry / Clinical data management / Drug safety / Electronic common technical document / Supplementary protection certificate / European Medicines Agency / Summary of Product Characteristics / Pharmacovigilance / Validation / Drug Master File
Date: 2016-07-20 07:22:57
Clinical research
Pharmaceutical industry
Clinical data management
Drug safety
Electronic common technical document
Supplementary protection certificate
European Medicines Agency
Summary of Product Characteristics
Pharmacovigilance
Validation
Drug Master File

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Source URL: www.ema.europa.eu

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