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Commission on Human Medicines
Results: 105

#	Item
91	CODE OF PRACTICE FOR CHAIRMEN AND MEMBERS OF THE COMMISSION ON HUMAN MEDICINES, CERTAIN SECTION 4 COMMITTEESAND EXPERT ADVISORY GROUPS Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2013-09-11 07:43:05 Pharmacy Clinical research Pharmaceutical industry Drug safety Medicines and Healthcare products Regulatory Agency British Pharmacopoeia Commission on Human Medicines Pharmacovigilance Pharmacopoeia Pharmaceutical sciences Pharmacology Health
92	Medicines Act 1968 Advisory Bodies Annual Reports[removed]Commission on Human Medicines Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2010-09-17 04:58:28 Pharmacology Clinical research Pharmaceutical industry Commission on Human Medicines Committee on Safety of Medicines Medicines and Healthcare products Regulatory Agency British Pharmacopoeia Adverse effect Alternative medicine Health Pharmaceutical sciences Medicine
93	Medicines Act 1968 Advisory Bodies Annual Reports 2007 Medicines Act 1968 Advisory Bodies Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2011-08-12 05:36:04 Pharmacy Clinical research Pharmaceutical industry Executive agencies of the United Kingdom government Commission on Human Medicines Committee on Safety of Medicines Medicines and Healthcare products Regulatory Agency British Pharmacopoeia Pharmacovigilance Pharmaceutical sciences Pharmacology Health
94	Resolution[removed]Countering fraudulent medicines, in particular their trafficking The Commission on Crime Prevention and Criminal Justice, Stressing that, for the purposes of the present resolution and without prejudice Add to Reading List Source URL: www.unodc.org Language: English - Date: 2013-02-19 08:31:48 Drug control law Drug policy Government Organized crime United Nations Office on Drugs and Crime International Narcotics Control Board Convention against Transnational Organized Crime United Nations Global Initiative to Fight Human Trafficking Law Human trafficking United Nations
95	Commission Implementing Regulation (EU) No[removed]of 7 March 2013 on the selection of a symbol for the purpose of identifying medicinal products for human use that are subject to additional monitoringText with EEA rele Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:55:12 Pharmacology Health Drug safety Pharmacy Pharmaceutical industry European Medicines Agency Pharmacovigilance Qualified Person Responsible For Pharmacovigilance Supplementary protection certificate Pharmaceuticals policy Pharmaceutical sciences Clinical research
96	Communication from the Commission — Detailed guidance on the request to the competent authorities for authorisation of a clinical trial on a medicinal product for human use, the notification of substantial amendments a Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:00:38 Pharmaceutical sciences Health Pharmacology Pharmaceutical industry European Union European Medicines Agency Clinical Trials Directive EudraLex EudraCT Clinical research Research Pharmaceuticals policy
97	Microsoft Word - FINAL summary report PEAG meeting held 27 Nov 2013.doc Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2014-02-05 11:53:39 Clinical research Pharmaceutical industry Organochlorides Pharmaceuticals policy Pharmacovigilance Yellow Card Scheme Medicines and Healthcare products Regulatory Agency European Medicines Agency Commission on Human Medicines Pharmaceutical sciences Pharmacology Health
98	Microsoft Word - Draft web minutes CHM 17 April 2014.doc Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2014-06-20 07:51:19 Drug safety Pharmacovigilance Pharmacy Commission on Human Medicines Academy of Medical Sciences Knights Bachelor Pharmaceutical sciences Pharmacology Health
99	SUMMARY MINUTES OF THE CLINICAL TRIALS, BIOLOGICALS & VACCINES (CTBVEAG) EXPERT ADVISORY GROUP HELD ON MONDAY 10 MARCH 2014 Information is being withheld, under Section 43 of the Freedom of Information Act 2000, on the g Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2014-04-16 10:47:47 Drug safety Pharmacovigilance Pharmacy Medicines and Healthcare products Regulatory Agency Commission on Human Medicines Pharmaceutical sciences Pharmacology Health
100	EUROPEAN COMMISSION ENTERPRISE AND INDUSTRY DIRECTORATE-GENERAL Tourism, CSR, Consumer Goods and International Regulatory Agreements Director Second meeting of the Steering Group on access to medicines Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2012-10-18 12:54:08 Brainstorming Human behavior Politics Behavior Biotechnology EuropaBio European Federation of Pharmaceutical Industries and Associations

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