Directive 2001 83 EC - PDFSEARCH.IO - Document Search Engine

Directive 2001 83 EC
Results: 312

#	Item
151	L[removed]EN Official Journal of the European Union Add to Reading List Source URL: www.fve.org Language: English - Date: 2014-06-03 16:50:36 Research Health Pharmacology European Medicines Agency Qualified Person Responsible For Pharmacovigilance Directive 2001/83/EC Pharmacovigilance Qualified Person Summary of Product Characteristics Pharmaceuticals policy Clinical research Pharmaceutical sciences
152	Comments on the Concept Paper submitted for Public Consultation concerning the Delegated Act on Principles and Guidelines of Good Manufacturing Practice for Active Substances in Medicinal Products for Human use. Ref: San Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:41:46 Pharmaceutical sciences Health policy EudraLex Good manufacturing practice Qualified Person Medicinal product Directive 2001/83/EC Validation Qualified Person for Pharmacovigilance Pharmaceuticals policy Clinical research Research
153	Official Journal L 311, [removed], p. 67 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:25:49 Health Research Pharmacology European Union Pharmaceutical industry Directive 2001/83/EC Directive 93/41/EEC Directive 75/319/EEC Directive 75/318/EEC Pharmaceuticals policy Clinical research Pharmaceutical sciences
154	Microsoft Word - DGentr-PH-COM_2002_735-F2PH311medicame_EN_ACTE.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:06:39 Research Pharmacology European Medicines Agency Pharmaceutical industry Pharmacovigilance Directive 2001/83/EC Good Laboratory Practice Qualified Person Responsible For Pharmacovigilance EudraLex Clinical research Pharmaceutical sciences Pharmaceuticals policy
155	Rue d’Arlon[removed]Brussels www.eucope.org European Commission DG SANCO/D/5 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:30:33 Health Pharmaceutical industry Pharmacology Drug safety Pharmacovigilance Marketing authorization Clinical trial Directive 2001/83/EC European Medicines Agency Pharmaceutical sciences Clinical research Pharmaceuticals policy
156	GVP Module Additional Monitoring Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2013-07-21 06:41:44 Pharmacology Pharmaceuticals policy Health Drug safety Pharmaceutical industry European Medicines Agency Pharmacovigilance Directive 2001/83/EC Summary of Product Characteristics Clinical research Pharmaceutical sciences Research
157	Microsoft Word - cermEU Certificate of GMP compliance of a manufacturerEMEA. Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:04:58 Pharmaceuticals policy Pharmacy Pharmaceutical industry Clinical research Good manufacturing practice Directive 2001/83/EC Tablet Dose Pharmaceutical sciences Dosage forms Pharmacology
158	[removed]EN Official Journal of the European Union Add to Reading List Source URL: www.fide-online.org Language: English - Date: 2008-01-14 05:08:37 Clinical research Technology Law European Union Medical Devices Directive Medical device CE mark Directive 2001/83/EC Undertakings for Collective Investment in Transferable Securities Directives European Union directives Pharmaceuticals policy Medicine
159	Directorate-General for the Presidency Directorate for Relations with National Parliaments Legislative Dialogue Unit Brussels, 5 March 2014 Add to Reading List Source URL: www.europarl.europa.eu Language: English - Date: 2014-03-07 06:02:19 Forms of government European Parliament Parliament Treaty of Lisbon Directive 2001/83/EC Law Government Politics
160	Official Journal L 311, [removed], p. 1 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:25:55 Health Pharmaceutical sciences Pharmacology Pharmaceutical industry European Union Directive 93/41/EEC Directive 2001/83/EC Marketing authorization Homeopathy Pharmaceuticals policy Clinical research Medicine

UPDATE