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Emergency Medicines List (EML). First Edition, November 2014 - Ethiopia

Food, Medicine and Health care Administration and Control Authority of Ethiopia (FMHACA) (2014) C_WHO
The list of emergency medicine has been developed though various consultative meeting and workshops with concerned health professionals and institutions. The medicines in the list should be administered to emergency patients only treated in the health institutions, purchased from legal medicine reta ... more
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List of Medicines for Community Pharmacy, Ethiopia (LMCP)

Food, Medicine and Health care Administration and Control Authority of Ethiopia (FMHACA) (2012) C1
Fourth Edition
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Chlorhexidine Cord Care Program in Nepal

Ministry of Health, Government of Nepal (2013) C1
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Epidemiological review of TB disease in Sierra Leone

L. Anderson and E. Hamblion World Health Organisation (WHO) (2015) C_WHO
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Nigeria Integrated Biological and Behavioural Surveillance Survey (IBBSS) 2014

National AIDS and STIs Control programme (NASCP), Federal Ministry of Health, Nigeria (2015) C1
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Post-sexual violence kits

Report the Abuse (2017) C1
Report the Abuse fact sheet
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Integrated Management of Neonatal and Childhood Illness - Treat the Young Infant and Counsel the Mother (Module 4/9)

World Health Organization WHO; UNICEF (2009) C_WHO
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India: Integrated Management of Neonatal and Childhood Illness (f-IMNCI) - Participant's Manual (Module 4/9)

Ministry of Health and Family Welfare, Government of India; WHO; UNICEF (2009) C_WHO
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India: Guidelines for Setting up Blood Storage Centres

National AIDS Control Organisation (NACO), Ministry of Health and Family Welfare, Government of India; National Blood Transfusion Council (NBTC) (2007) C1
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Treatment of tuberculosis guidelines. Russian version

World Health Organization (2009)
4th edition
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india: Guidelines for Storage of 2nd -Line Anti-TB-Drugs for Revised National TB Control Programme (RNTCP)

Government of India, Central Tuberculosis Division, Ministry of Health and Family Welfare (2011) C1
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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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GLI Practical Guide to TB Laboratory Strengthening

Global Laboratory Initiative World Health Organization (2017) C_WHO
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Ghana: GUIDELINES FOR REPORTING ADVERSE REACTION

Food and Drugs Authority (FDA), Ghana (2016) C2
Document No. : FDA/SMC/SMD/GL-RAR/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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The shorter MDR-TB regimen

World Health Organization (2016) C_WHO
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Monitoring and Evaluation of National Action Plans on AMR

World Health Organization WHO (2017) C_WHO
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A Guide to the Registration, Licensing and Scheduling of Medicinal Products in Malawi

Pharmacy, Medicines and Poisons Board, Malawi (2002) C2
First edition, November 1997 | Revised July 2002
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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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Nigeria: GOOD PRACTICES FOR PHARMACEUTICAL QUALITY CONTROL LABORATORIES

National Agency for Food and Drugs Administration and Control (NAFDAC) (2016) C2