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191	E.02 CMDv RfR Oct-Nov 12 EMA-CMDv[removed] Add to Reading List Source URL: www.hma.eu Language: English - Date: 2013-02-07 05:40:50 Pharmaceutical industry Health European Medicines Agency Vaccine EudraLex Pharmaceutical sciences Clinical research Pharmaceuticals policy Research
192	EUROPEAN COMMISSION HEALTH QND CONSUMERS DIRECTORATE-GENERAL Director General Brussels, Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:04:07 Clinical research Drug safety Pharmacy European Medicines Agency Pharmacovigilance Veterinary physician Veterinary Medicines Directorate EudraLex Pharmaceutical sciences Pharmacology Health
193	Microsoft PowerPoint - 13 HOLM Anja (EMA) EMA.ppt [Mode de compatibilité] Add to Reading List Source URL: www.rr-africa.oie.int Language: English - Date: 2010-11-24 09:14:54 Pharmaceutical sciences Pharmacology European Medicines Agency EudraLex European Directorate for the Quality of Medicines Pharmacovigilance Qualified Person Qualified Person Responsible For Pharmacovigilance Good Clinical Practice Directive Clinical research Pharmaceuticals policy Research
194	FERNAND SAUER HOPES AND RISKS:THE CASE OF PHARMACEUTICALS domain there is also a great degree of irrationality and beliefs, especially when people turn to traditional remedies and alternative medicines because they are Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2012-03-20 15:12:59 Pharmaceuticals policy Clinical research Pharmacy European Union law Pharmacovigilance Food and Drug Administration Precautionary principle EudraLex Pharmaceutical industry Pharmaceutical sciences Pharmacology Health
195	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA PHARM 618 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:48:36 Pharmaceutical sciences Health EudraLex Directive 2001/83/EC Pharmacovigilance Qualified Person Responsible For Pharmacovigilance Regulation Directive Medicinal product Pharmaceuticals policy Clinical research Research
196	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – Quality, safety and efficacy PHARM 633 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-11-21 03:31:56 Research Pharmaceutical sciences Health European Union directives European Medicines Agency EudraLex EudraGMP Good manufacturing practice Clinical Trials Directive Pharmaceuticals policy Clinical research Pharmaceutical industry
197	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – Quality, safety and efficacy PHARM 644 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-05-05 07:48:08 Research European Union Government European Medicines Agency Pharmaceutical industry EudraLex Clinical Trials Directive Council Implementing Regulation (EU) No 282/2011 Clinical research European Union directives Pharmaceuticals policy
198	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA PHARM 639 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-02-12 05:22:25 Health Pharmaceutical industry Drug safety Pharmacy Pharmaceuticals policy European Medicines Agency Pharmacovigilance Biosimilar EudraLex Pharmaceutical sciences Pharmacology Clinical research
199	Study on the environmental risks of medicinal products FINAL REPORT Executive Agency for Health and Consumers 12 December 2013 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-06-17 09:17:47 Pharmacology Pharmacy Pharmaceuticals policy Clinical research Pharmacovigilance Committee for Medicinal Products for Human Use European Medicines Agency EudraLex Pharmaceutical sciences Health Drug safety
200	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, European Medicines Agency PHARM 643 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-05-05 07:48:08 Pharmaceutical sciences Health Directive 65/65/EEC European Medicines Agency EudraLex Supplementary protection certificate Pharmaceuticals policy Clinical research Research

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