![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 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](https://www.pdfsearch.io/img/1b6e1a94d3d69418020326eab1a02996.jpg) Date: 2013-07-12 06:13:47Pharmaceuticals 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 Add to Reading ListSource URL: www.jazmp.siDownload Document from Source Website File Size: 532,18 KBShare Document on Facebook
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