Directive 75 318 EEC - PDFSEARCH.IO - Document Search Engine

Directive 75 318 EEC
Results: 69

#	Item
41	Microsoft Word - CMDv report for release February[removed]final Add to Reading List Source URL: www.hma.eu Language: English - Date: 2009-02-25 10:35:43 European Medicines Agency Pharmaceutical industry Pharmaceutical sciences Government Directive 75/318/EEC Supplementary protection certificate Clinical research Pharmaceuticals policy Research
42	The rules governing cosmetic products in the European Union Volume 2 Cosmetics legislation Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-07-03 11:50:04 Standards Pharmaceuticals policy Safety Cosmetics Cosmetics Directive ISIRI 13146 Directive 75/318/EEC Evaluation European Union directives Reference
43	Directive[removed]EC of the European Parliament and of the Council of 18 June 2009 amending Directive[removed]EC and Directive[removed]EC, as regards variations to the terms of marketing authorisations for medicinal pro Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:52:57 European Union Health policy Health Directive 2001/83/EC European Medicines Agency Directive 75/318/EEC Directive on intra-EU-transfers of defence-related products Pharmaceuticals policy Clinical research Research
44	L[removed]EN Official Journal of the European Communities Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2012-03-20 15:11:38 Law Europe Clinical research Battery Directive Directive 75/318/EEC European Union directives Pharmaceuticals policy European Union
45	Microsoft Word - Summary record 12th meeting VETPHARM 223 final.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:25:44 Research Health Pharmacovigilance Directive 75/318/EEC European Directorate for the Quality of Medicines Directive 2001/83/EC EudraLex European Medicines Agency Pharmaceuticals policy Clinical research Pharmaceutical sciences
46	Microsoft Word - Update-Declaration-TBT_MRA_Good_Clinical_Practice.doc Add to Reading List Source URL: www.efta.int Language: English - Date: 2013-05-28 10:56:19 Pharmaceutical sciences Science Clinical trial Good Clinical Practice Directive 75/318/EEC Clinical research Pharmaceutical industry Research
47	Microsoft Word - VETPHARM 200 Draft record meeting 25 October 2000 correcte. Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:25:02 Pharmacology Council of Europe Health Pharmacy Clinical research European Directorate for the Quality of Medicines Directive 75/318/EEC Pharmacovigilance European Pharmacopoeia Pharmaceutical sciences Medicine Pharmaceuticals policy
48	ANNEX E Seeds (Art. 11) ARTICLE 1 Scope This Annex applies to seeds of agricultural species covered by the legal acts listed in Add to Reading List Source URL: www.efta.int Language: English - Date: 2013-05-28 10:56:09 Reference Standards European Union law Law Copyright law of the European Union ISIRI 13146 Directive 75/318/EEC European Union directives Pharmaceuticals policy Evaluation
49	EUROPEAN COMMISSION DIRECTORATE-GENERAL III INDUSTRY Industrial affairs III: Consumer goods industries Pharmaceuticals and cosmetics Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:25:02 Health Research Qualified Person Responsible For Pharmacovigilance Pharmacovigilance Directive 75/318/EEC European Directorate for the Quality of Medicines European Medicines Agency Qualified Person Directive 93/41/EEC Pharmaceuticals policy Clinical research Pharmaceutical sciences
50	L[removed]EN Official Journal of the European Communities Add to Reading List Source URL: www.help-button.co.uk Language: English - Date: 2010-12-02 14:07:20 Technology CE mark Medical Devices Directive Internal Market Directive Medical device Type approval Common technical regulation Directive 75/318/EEC European Union directives European Union Medicine

UPDATE