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Nigeria: National Drug Policy

Ministry of Health , World Health Organisation (WHO) (2005) C_WHO
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National Drug Distribution Guidelines 2nd Edition 2012

Federal Ministry of Health, Nigeria (2012) C1
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The fight against fake drugs by NAFDAC in Nigeria Olike Chinwendu KIT (Royal Tropical Institute) Development Policy & Practice Vrije Universiteit Amsterdam (2008) CC
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Guidelines for Good Clinical Practice (GCP) for Trials on Pharmaceutical Products Bangladesh

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Sierra Leone: Supply chain assessment for ARV drugs and HIV test kits

Allers, Claudia, Timothy O’Hearn, and Meba Kagone USAID (2007) C1
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Sierra Leone - Pharmaceutical Sector Country Profile (Questionnaire 2011)

World Health Organization (WHO); The Global Fund (2011) C_WHO
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Pharmacopoeia Commission for Indian Medicine & Homoeopathy, Ministry of AYUSH, Government of India (2016) C1
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Medicine Prices, Availability and Affordability Survey Haiti

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Nepal Pharmaceutical Country Profile

World Health Organisation (WHO), Ministry of Health Nepal (2011) C_WHO
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Comparative Analysis of Pharmacovigilance Systems in Five Asian Countries

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Central Sector Scheme on Conservation, Development and Sustainable Management of Medicinal Plants

Goverment of India, Ministry of Ayush, National Medicinal Plants Board (2015) C1
Operational Guidelines
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Lesotho Pharmaceutical Country Profile

Ministry of Health and Social Welfare, World Health Organization (WHO) Lesotho Country Office (2011) C1
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Malawi - Pharmaceutical Sector Country Profile (Questionnaire 2011)

World Health Organization (2011) C_WHO
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Kenya Health Assessment 2010

USAID, SPS, Strengthening Pharmaceutical Systems Program-Kenya (2010) C1
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Zambia: THE MEDICINES AND ALLIED SUBSTANCES ACT, 2013

The Government of Zambia (2013) C1
Medicines and Allied Substances [No. 3 of 2013 47 | An Act to continue the existence of the Pharmaceutical Regulatory Authority and re-name it as the Zambia Medicines Regulatory Authority; provide for the functions and powers of the Authority; provide for the registration and regulation of pharmacie... more
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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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South Africa: GUIDELINES FOR THE REGISTRATION OF MEDICINES

Medicines Control Council (MCC), Department of Health Republic of South Africa (2012) C1
This guideline is intended to provide recommendations to applicants wishing to submit applications for the registration of medicines. It represents the Medicines Control Council’s current thinking on the safety, quality and efficacy of medicines.
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Uganda: Annual Pharmacovigilance Report July 2015 – June 2016

National Drug Authority, Uganda (2016) C1
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Senegal private health sector assessment: Selected health products and services

Brunner B., J. Barnes, A. Carmona et. al. United States Agency for International Development (2016) C2
SHOPS and HIA finalized a scope of work with USAID Senegal in April 2015, and a team of five private sector experts conducted the onsite assessments between May and June 2015. The Private Sector Assessment (PSA) team worked closely with Senegalese key stakeholders throughout the process. The PSA tea... more