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

Pharmacy Board Sierra Leone (2014) C1
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Nigeria: National Guideline for the Control and Management of Sickle Cell Disease

Federal Ministry of Health, Nigeria (2014) C1
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Liberia: Definitions of Indicators: Essential Health Services

Ministry of Health, Liberia; World Health Organization (WHO) (2016) C_WHO
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India: Guidelines on Prevention and Management of TB in PLHIV at ART Centres

National AIDS Control Organisation (NACO), Ministry of Health & Family Welfare, Government of India (2016) C1
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India: Guidelines on Airborne Infection Control in Healthcare and Other Settings

Directorate General of Health Services , Ministry of Health & Family Welfare, Government of India (2010) C1
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India: Guidelines for Postexposure Chemoprophylaxis

Central Leprosy DivisionNLEP, Ministry of Health and Family Welfare, Government of India (2016) C1
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Ethiopia: GUIDELINE ON MEASLES SURVEILLANCE AND OUTBREAK MANAGEMENT

Ethiopian Health and Nutrition Research Institute, Federal Democratic Republic of Ethiopia (2012) C1
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GUIDELINES FOR ONCHOCERCIASIS ELIMINATION IN ETHIOPIA

Federal Ministry of Health, Ethiopia (2015) C1
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Treatment of tuberculosis - Annex 3 Grade evidence profiles

World Health Organization (2017) C_WHO
Guidelines for treatment of drug-susceptible tuberculosis and patient care 2017 update
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Treatment of tuberculosis - Annex 4 Evidence- to- decision tables

World Health Organization (2017) C_WHO
Guidelines for treatment of drug-susceptible tuberculosis and patient care Update 2017
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Treatment of tuberculosis - Annex 6 Essential first-line antituberculosis drugs

World Health Organization (2017) C_WHO
Guidelines for treatment of drug-susceptible tuberculosis and patient care Uptsate 2017
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GUIDELINES FOR CONDUCTING CLINICAL TRIALS OF MEDICINES, FOOD SUPPLEMENTS, VACCINES AND MEDICAL DEVICES IN GHANA

Food and Drugs Authority (FDA), Ghana (2013) C1
Document No. : FDA/SMC/CTD/GL-CCT/2013/01
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Guidelines for conduct of clinical trials in Kenya

Pharmacy and Poisons Board, Ministry of Health, Kenya (2016) C1
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Summary of product charakteristics - annex 1

European Medicines Agency (2017) C2
Accessed November 2017
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Uganda: Guidelines on good manufacturing practice for medicinal products - ANNEXES

National Drug Authority (NDA), Uganda (2017) C1
Doc. No.: INS/GDL/001-(Annexes)
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Zambia: GUIDELINES ON REGULATING THE CONDUCT OF CLINICAL TRIAL IN HUMAN PARTICIPANTS

Zambia Medicines Regulatory Authority (ZAMRA) (2016) C2
First Edition
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Zambia: GENERAL GUIDELINES FOR SUBMITTING APPLICATIONS FOR REGISTRATION OF A MEDICINE

Zambia Medicines Regulatory Authority (ZAMRA) (2016) C2
First Edition
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GUIDELINE ON SUBMISSION OF DOCUMENTATION FOR REGISTRATION OF A MULTISOURCE (GENERIC) FINISHED PHARMACEUTICAL PRODUCT (FPP): QUALITY PART IN THE COMMON TECHNICAL DOCUMENT (CTD) FORMAT

Medicines Control Authority of Zimbabwe (MCAZ) (2012) C2
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South Africa: National Parenteral Nutrition Practice Guidelines for Paediatrics

National Department of Health, Republic of South Africa (2016) C2
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South Africa: Cold Chain and Immunisation Operations Manual

Department of Health, Republic of South Africa (2015) C2
Guidelines for Handling Temperature Sensitive Vaccines and Pharmaceuticals