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Consumers Research
Results: 848

#	Item
641	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, European Medicines Agency PHARM 648 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-05-05 07:48:08 Pharmacology Health Drug safety Pharmacy European Medicines Agency Pharmacovigilance Directive 2001/83/EC Qualified Person Responsible For Pharmacovigilance Supplementary protection certificate Pharmaceuticals policy Clinical research Pharmaceutical sciences
642	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, European Medicines Agency PHARM 630 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-30 04:33:16 Research Pharmaceuticals policy Pharmaceutical industry Biologic European Medicines Agency Biosimilar Pharmacovigilance Directive 2001/83/EC Medicinal product Pharmacology Pharmaceutical sciences Clinical research
643	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
644	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
645	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, European Medicines Agency PHARM 658 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-05-05 07:46:09 Pharmaceutical industry Pharmacy European Medicines Agency Biosimilar Food and Drug Administration Pharmaceutical sciences Pharmacology Clinical research
646	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA PHARM 635 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-30 04:33:16 Pharmacology Health Drug safety Pharmacy Pharmacovigilance European Medicines Agency Directive 2001/83/EC Qualified Person Responsible For Pharmacovigilance Qualified Person for Pharmacovigilance Pharmaceutical sciences Clinical research Pharmaceuticals policy
647	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA PHARM 631 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-30 04:33:16 Pharmaceutical sciences Pharmacology Pharmaceutical industry Executive agencies of the United Kingdom government Drug safety European Medicines Agency EudraLex Clinical research Pharmaceuticals policy Research
648	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA PHARM 641 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-05-05 07:48:07 European Medicines Agency Pharmaceutical industry Pharmaceutical sciences Health Directive 2001/83/EC Octapharma Research exemption Supplementary protection certificate Clinical research Pharmaceuticals policy Research
649	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA PHARM 625 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:46:43 Pharmacology Health Pharmaceutical industry Drug safety European Medicines Agency Pharmacovigilance Good manufacturing practice Validation International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmaceutical sciences Pharmaceuticals policy Clinical research
650	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, European Medicines Agency PHARM 655 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-05-05 07:45:51 Pharmaceutical industry Health European Medicines Agency Alternative medicine Off-label use Pharmacovigilance Supplementary protection certificate Pharmaceutical sciences Pharmacology Clinical research

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