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Pharmaceuticals policy / Health / Medical research / Clinical Trials Directive / Directive 2001/83/EC / Good laboratory practice / Marketing authorization / Good Clinical Practice Directive / European Pharmacopoeia / Biopharmaceutical / Pharmacovigilance / European Medicines Agency
Date: 2013-07-12 06:13:47
Pharmaceuticals policy
Health
Medical research
Clinical Trials Directive
Directive 2001/83/EC
Good laboratory practice
Marketing authorization
Good Clinical Practice Directive
European Pharmacopoeia
Biopharmaceutical
Pharmacovigilance
European Medicines Agency

The Agency for Medicinal Products and Medical Devices of the Republic of Slovenia has prepared the unofficial consolidated text for the Medicinal Products Act which includes:  Medicinal Products Act (Official Gazette

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