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State Strategy to Combat the Spread of HIV in Russia through 2020 and beyond

Federal Government (2016) C2
Unofficial Translation Approved by the Federal Government on October 20, 2016
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Essential Medicines and Health Supplies List for Uganda (EMHSLU) 2016

Ministry of Health Uganda (2016) C1
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WHO guidelines for the treatment of Treponema pallidum (syphilis)
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World Health Organization WHO (2016) C_WHO
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Zika Virus Research Agenda - October 2016

World Health Organization WHO (2016) C_WHO
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Review of the HIV Programme in the former Yugoslav Republic of Macedonia

D. Raben; S. F.Jakobsen; A. Sönnerborg; E. Subata World Health Organization (Europe); Research Gate (2016) C_WHO
October 2015
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The growing HIV epidemic in Central Europe: a neglected issue?

D. Gökengin; C. Oprea; S. Uysal; J. Begovac PMC - US National Library of Medicine National Institutes of Health; Journal of Virus Eradication (2016) C2
Review Journal of Virus Eradication 2016 Jul; 2(3): 156–161. Published online 2016 Jul 1. PMCID: PMC4967967 PMID: 27482455
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The Global State of Harm Reduction 2016

K. Stone; G. Sander Harm Reduction International (2016) C2
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Lymphatic Filariasis and Podoconiosis morbidity management and disability prevention guidelines
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Ministry of Health Ethiopia (2016) CC
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Ghana: GUIDELINES FOR REPORTING ADVERSE REACTION

Food and Drugs Authority (FDA), Ghana (2016) C2
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The use of molecular line probe assays for the detection of resistance to isoniazid and rifampicin

World Health Organization (2016) C_WHO
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Ghana: GUIDELINES FOR SAFETY MONITORING OF MEDICINAL PRODUCTS

Food and Drug Authority (FDA), Ghana (2016) C2
Document No. : FDA/SMC/SMD/GL-SMP/2015/05 | These guidelines are for information, guidance and strict compliance by Marketing Authorization Holders and Local Representatives of regulated products to help in the continuous safety monitoring of products granted marketing authorization in Ghana.
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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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Zambia: GUIDELINES ON REGULATING THE CONDUCT OF CLINICAL TRIAL IN HUMAN PARTICIPANTS

Zambia Medicines Regulatory Authority (ZAMRA) (2016) C2
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Zambia: APPLICATION FOR MARKETING AUTHORISATION OF CONDOMS

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

Zambia Medicines Regulatory Authority (ZAMRA) (2016) C2
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Zimbabwe National Pharmacovigilance Policy Handbook, 2nd ed.

Medicines Control Authority of Zimbabwe (MCAZ) | Ministry of Health and Child Care (2016) C2
The Zimbabwe National Pharmacovigilance Policy Handbook, 2nd Edition updates the November 2013 version to indicate the Zimbabwe National Pharmacovigilance (PV) Centre’s compliance with the WHO Pharmacovigilance Indicators Handbook 2015.
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SWAZILAND GUIDELINE ON DONATION OF MEDICINES

Ministry of Health, Kingdom of Swaziland (2016) C2
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Swaziland: MEDICINES AND RELATED SUBSTANCES CONTROL ACT, 2016

Government of the Kingdom of Swaziland (2016) C2
Act 9 of 2016
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Technical and Operational Guidelines (TOG) for TB Control in India 2016 - Annexures & Appendix

Government of India, Central Tuberculosis Division, Ministry of Health and Family Welfare (2016) C1
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The use of molecular line probe assays for the detection of resistance to second-line anti-tuberculosis drugs

World Health Organization (2016) C_WHO
Policy Guidance.