Commission on Human Medicines

Results: 105



#Item
91CODE OF PRACTICE FOR CHAIRMEN AND MEMBERS OF THE COMMISSION ON HUMAN MEDICINES, CERTAIN SECTION 4 COMMITTEESAND EXPERT ADVISORY GROUPS

CODE OF PRACTICE FOR CHAIRMEN AND MEMBERS OF THE COMMISSION ON HUMAN MEDICINES, CERTAIN SECTION 4 COMMITTEESAND EXPERT ADVISORY GROUPS

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Source URL: www.mhra.gov.uk

Language: English - Date: 2013-09-11 07:43:05
92Medicines Act 1968 Advisory Bodies Annual Reports[removed]Commission on Human Medicines

Medicines Act 1968 Advisory Bodies Annual Reports[removed]Commission on Human Medicines

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Source URL: www.mhra.gov.uk

Language: English - Date: 2010-09-17 04:58:28
93Medicines Act 1968 Advisory Bodies Annual Reports 2007 Medicines Act 1968 Advisory Bodies

Medicines Act 1968 Advisory Bodies Annual Reports 2007 Medicines Act 1968 Advisory Bodies

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Source URL: www.mhra.gov.uk

Language: English - Date: 2011-08-12 05:36:04
94Resolution[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

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

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Source URL: www.unodc.org

Language: English - Date: 2013-02-19 08:31:48
95Commission 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

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

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Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 08:55:12
96Communication 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

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

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Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 09:00:38
97Microsoft Word - FINAL summary report PEAG meeting held 27 Nov 2013.doc

Microsoft Word - FINAL summary report PEAG meeting held 27 Nov 2013.doc

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Source URL: www.mhra.gov.uk

Language: English - Date: 2014-02-05 11:53:39
98Microsoft Word - Draft web minutes CHM 17 April 2014.doc

Microsoft Word - Draft web minutes CHM 17 April 2014.doc

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Source URL: www.mhra.gov.uk

Language: English - Date: 2014-06-20 07:51:19
99SUMMARY 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

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

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Source URL: www.mhra.gov.uk

Language: English - Date: 2014-04-16 10:47:47
100EUROPEAN 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

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

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Source URL: ec.europa.eu

Language: English - Date: 2012-10-18 12:54:08