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101 documents on 3 pages
 
 
 
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2nd Biennial Scientific Conference on Medicines Regulation in Africa. Addis Ababa, Ethiopia, 30th November to 1st December 2015 - Book of Abstracts. Conference Theme: Regulatory Systems Strengthening for advancing Research, Innovation and Local Pharmaceutical Production in Africa

Year:

2015;

Pages:

38;


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An Antibiotic’s Journey from Marketing Authorization to Use, Norway (Bull World Health Organ 2017;95:220–226)

Year:

2017;

Pages:

7;


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Collaboration, Not Competition: Developing New Reliance Models - Regulatory Collaboration. Exchange of Assessment Reports (ARs) with Regulators Outside the European Union (EU). (WHO Drug Information Vol. 30, No. 4, 2016)

Year:

2017;

Pages:

9;


 
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Collaborative Procedure Between the World Health Organization (WHO) Prequalification Team and National Regulatory Authorities in the Assessment and Accelerated National Registration of WHO-prequalified Pharmaceutical Products and Vaccines. WHO Technical Report Series, No. 996, 2016, Annex 8

Year:

2016;

Pages:

42;


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Comparison of Medicines Legislation in the East African Community - Medicines Regulation. (WHO Drug Information Vol. 30, No. 4, 2016)

Year:

2017;

Pages:

10;


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Compendium of Medicines Evaluation and Registration for Medicine Regulation Harmonization in The East African Community, 2014

Year:

2014;

Pages:

312;


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Compendium of Quality Management System (QMS) Technical Documents for Harmonization of Medicines Regulation in the East African Community, 2104

Year:

2014;

Pages:

172;


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Drug Registration Guidance 2073. (Issued under Drug Registration Regulation 2038). MOH, Nepal, 2016

Year:

2016;

Pages:

177;


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First Biennial Scientific Conference on Medicines Regulation in Africa. Johannesburg, Afrique du Sud, 2–3 December 2013 - Book of Abstracts. Conference Theme: Building Partnerships for Sustainable Capacity Development in Medicines Regulation in Africa [French]

Year:

2013;

Pages:

72;


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First Biennial Scientific Conference on Medicines Regulation in Africa. Johannesburg, South Africa, 2-3 December, 2013 - Conference Report. Conference Theme: Building Partnerships for Sustainable Capacity Development in Medicines Regulation in Africa

Year:

2013;

Pages:

84;


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Guidance on Good Practices for Desk Assessment of Compliance with Good Manufacturing Practices, Good Laboratory Practices and Good Clinical Practices for Medical Products Regulatory Decisions. WHO Technical Report Series, No. 1010, 2018, Annex 9

Year:

2018;

Pages:

38;


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Guidelines for Conducting Clinical Trials - Sierra Leone

Year:

2013;

Pages:

14;


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Guidelines for Conducting Clinical Trials of Medicines, Food Supplements, Vaccines and Medical Devices in Sierra Leone

Year:

2014;

Pages:

32;


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Guidelines for Medicinal Product Registration - Sierra Leone

Year:

2013;

Pages:

28;


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Guidelines on Regulatory Preparedness for Provision of Marketing Authorization of Human Pandemic Influenza Vaccines in Non-vaccine-producing Countries. WHO Expert Committee on Biological Standardization, Sixty-seventh Report; WHO Technical Report Series No. 1004, 2017, Annex 7

Year:

2017;

Pages:

29;


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Legislación reglamentaria nacional en materia de fármacos: Principios orientadores para pequeños servicios de reglamentación farmacéutica. OMS, Serie de Informes Técnicos, No. 885, 1999, Annex 8 [English]

Year:

1999;

Pages:

44;


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