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2700
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Petunjuk Praktis Terapi Insulin pada Pasien Diabetes Melitus

Indonesian Society of Internal Medicine (2006) C1
Practical Guidelines of Insulin Therapy in Diabetes Mellitus Patients
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Keputusan Menteri Kesehatan Republik Indonesia Nomor 2500/MENKES/SK/XII /2011 tentang Daftar Obat Esensial Nasional 2011

Ministry of Health Republic of Indonesia (2011) C1
Decree of the Minister of Health of the Republic of Indonesia No. 2500 / MENKES / SK / XII / 2011 on National Essential Medicines List 2011
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Instruksi Presiden Republik Indonesia Nomor 3 tahun 2002 tentang Penanggulangan Penyalahgunaan dan Peredaran Gelap Narkotika, Psikotropika, Prekursor dan Zat Adiktif Lainnya

President of the Republic of Indonesia (2002) C1
Instruction of the President of the Republic of Indonesia No. 3 of 2002 concerning the Control of Illicit Abuse and Distribution of Narcotics, Psychotropic, Precursors and other Addictive Substances
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Keputusan Menteri Kesehatan Republik Indonesia tentang Pedoman Penyelanggaraan Sarana Pelayanan Rehabilitasi Penyalahgunaan dan Ketergantungan Narkotika, Psikotropika dan Zat Adiktif Lainnya (NAPZA)

Ministry of Health Republic of Indonesia (2002) C1
Decree of the Minister of Health of the Republic of Indonesia on Guidelines for the Arrangement of Service Facilities for the Rehabilitation of Abuse and Addiction of Narcotics, Psychotropic and other Addictive Substances
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Keputusan Menteri Kesehatan Republik Indonesia tentang Penetapan Rumah Sakit dan Satelit Uji Coba Pelayanan Terapi Rumatan Metadon serta Pedoman Program Terapi Rumatan Metadon

Ministry of Health Republic of Indonesia (2006) C1
Decree of the Minister of Health of the Republic of Indonesia on the Establishment of Hospitals and Satellite Test of Methadone Therapy Service and Program Guidelines for Methadone Maintenance Therapy
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Undang-Undang Republik Indonesia Nomor 35 Tahun 2009 tentang Narkotika

President of the Republic of Indonesia (2009) C1
Law of the Republic of Indonesia on Narcotics
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Peraturan Menteri Kesehatan Republik Indonesia Nomor 55 Tahun 2015 tentang Pengurangan Dampak Buruk Pada Pengguna NAPZA Suntik

Ministry of Health Republic of Indonesia (2015) C1
Regulation of the Minister of Health of the Republic of Indonesia on Impact Reduction for Injecting Narcotics Drug Users NAPZA : Narkotika, Psikotropika dan Zat Adiktif Lainnya (Narcotics, Psychotropic and Other Addictive Substances)
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Peraturan Pemerintah Republik Indonesia Nomor 72 Tahun 1998 tentang Pengamanan Sediaan Farmasi dan Alat Kesehatan

President of the Republic of Indonesia (1998) C1
Government Regulation of the Republic of Indonesia regarding Security of Pharmaceutical Preparations and Medical Equipments
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Política Nacional de Medicamentos Paraguay 2015
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Pan American Health Organization PAHO; World Health Organization, Regional Office for the Americas (2016) C_WHO
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Guidelines for Registration of Medicines and Health Products in Liberia

Liberia Medicines and Health Products Regulatory Authority (LMHRA) (2012) C1
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National Antibiotic Treatment Guideline (Nepal)

Government of Nepal; Ministry of Health and Population (2014) C1
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Botswana National Drugs (Medicine) Policy

Ministry of Health, Gabarone, Botswana (2005) C2
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Ethiopia: Standard Treatment Guidelines for Health Center

Drug Administration and Control Authority of Ethiopia Contents (2014) C1
3rd edition
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Botswana: Guidelines on Good Manufacturing Practices

Ministry of Health, Gabarone, Botswana (2009) C2
Drug Advisory Board
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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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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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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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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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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