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European Medicines Agency / Government / Pharmaceutical sciences / Directive 2001/83/EC / Qualified Person Responsible For Pharmacovigilance / Supplementary protection certificate / Clinical research / Pharmaceuticals policy / Research
Date: 2013-10-09 09:07:11
European Medicines Agency
Government
Pharmaceutical sciences
Directive 2001/83/EC
Qualified Person Responsible For Pharmacovigilance
Supplementary protection certificate
Clinical research
Pharmaceuticals policy
Research

Microsoft Word - EMEA comments on draft Regulation

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