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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