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Namibia Health Facility Census 2009: Key Findings on Family Planning, Maternal and Child Health, and Malaria

Ministry of Health and Social Services (MoHSS), Namibia; ICF Macro, USA (2010) C_WHO
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Namibia Health Facility Census 2009: Key Findings on HIV/AIDS, TB and STIs

Ministry of Health and Social Services (MoHSS), Namibia; ICF Macro, USA (2010) C_WHO
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Namibia 2011 Census Disability Report

Namibia Statistics Agency (2016) C2
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ALGORITHMS FOR HIV CARE AND TREATMENT IN ETHIOPIA, HIVCore Final Report

Kalibala Samuel, Nrupa Jani and Getachew Kassa United States Agency for International Development (USAID) (2016) C1
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Ethiopia: GUIDELINE FOR IMPLEMENTATION OF A PATIENT REFERRAL SYSTEM

Federal Ministry of Health, Ethiopia (2010) C1
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Namibia: National Tuberculosis and Leprosy Programme (2015-2016)

Ministry of Health and Social Services (MOHSS) (2016) C1
Annual Report: 2015-2016
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Personal protective equipment for use in a filovirus disease outbreak
recommended

World Health Organization WHO (2016) C_WHO
Rapid Advice Guideline
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NAMIBIA 2014/15 HEALTH ACCOUNTS REPORT

Ministry of Health and Social Services (MOHSS) (2017) C2
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Annual Health Sector Performance Report 2016/2017

Ministry of Health Uganda (2017) C1
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Uganda: Management of Tuberculosis in Children
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Ministry of Health, Republic of Uganda | NtlP (2015) C2
A health worker guide.
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Botswana: Guidelines for stability testing of pharmaceutical products

Ministry of Health, Gabarone, Botswana (2009) C2
This guideline is intended to provide requirements to applicants wishing to submit applications for registration of medicines in Botswana.
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WHO Meeting Report of a Technical Expert Consultation: Non-inferiority analysis of Xpert MTB/RIF Ultra compared to Xpert MTB/RIF

World Health Organization (2017) C_WHO
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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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Laws of Kenya- - PHARMACY AND POISONS ACT

National Council for Law Reporting with the Authority of the Attorney-General Kenya Law Reports (KLR) (2012) C2
CHAPTER 244
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Monitoring and Evaluation of National Action Plans on AMR

World Health Organization WHO (2017) C_WHO
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PHARMACY, MEDICINES AND POISONS BOARD GOOD MANUFACTURING PRACTICES GUIDELINES(GMP) (Malawi)

Pharmacy, Medicines & Poisons Board, Malawi (2013) C2
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Namibia: Application for Registration of a Medicine

Ministry of Health and Social Services (MOHSS) (2014) C2
Namibia guideline for submission of applications for registration of pharmaceuticals for human use in common technical document format.
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GOOD MANUFACTURING PRACTICE GUIDELINES FOR PHARMACEUTICAL PRODUCTS

National Agency for Food and Drugs Administration and Control (NAFDAC), Nigeria (2016) C2
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Zambia: APPLICATION FOR MARKETING AUTHORISATION OF CONDOMS

Zambia Medicines Regulatory Authority (ZAMRA) (2016) C2
Guidance for the preparation and submission of dossiers
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Zambia: GENERAL GUIDELINES FOR SUBMITTING APPLICATIONS FOR REGISTRATION OF A MEDICINE

Zambia Medicines Regulatory Authority (ZAMRA) (2016) C2
First Edition