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Siveyans Danje nan kominote a Manadje Gid

Organización Panamericana de la Salud (2016) C1
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Aufklärungsinformation zur Impfung gegen Tetanus, Diphtherie, Pertussis und Poliomyelitis (Tdap-IPV) in 15 Sprachen

Robert-Koch-Institut RKI; Deutsches Grünes Kreuz (2015) C1
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National Guidelines for HIV Prevention Treatment and Care

Federal Ministry of Health, Abuja, Nigeria (2016) C1
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Sudah Siapkah Kita Menghadapi Gempa Bumi?

Ministry of Health Republic of Indonesia, WHO (2016) C_WHO
Guidance book about implementation of health crisis response for school children in Indonesia in facing earthquake as natural disaster
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Sudah Siapkah Kita Menghadapi Banjir?

Ministry of Health Republic of Indonesia, WHO (2016) C_WHO
Are we ready to face the flood? This book contains general knowledge about the flood, the efforts made before, during, and after the flood and what things can be done by children and adolescents while in evacuation. This book is done specifically for school children in Indonesia
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Sudah Siapkah Kita Menghadapi Tanah Longsor?

Ministry of Health Republic of Indonesia, WHO (2016) C_WHO
Are we ready to face landslide? A manual book of health crisis response for school children in facing landslide as a potential natural disaster in Indonesia
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2015 Pipeline Report HIV, Hepatitis C virus (HCV), and Tuberculosis (TB)

Polly Clayden, Simon Collins, Mike Frick, et al. A. Benzacar; HIV i-BASETREATMENT ACTION GROUP (2015)
Drugs, Diagnostics, Vaccines, Preventive Technologies, Research toward a cure, and immune-based and gene therapies in development
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Pharmacopoeia Commission for Indian Medicine & Homoeopathy, Ministry of AYUSH, Government of India (2016) C1
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Drug Resistance Through The Back Door: How The Pharmaceutical Industry Is Fuelling The Rise Of Superbugs Through Pollution In Its Supply Chains

Sascha Marchang, Natasha Hurley European Public Health Alliance (EPHA), Changing Markets (2016) C1
Irresponsible pharmaceutical companies fuel the proliferation of superbugs through supply chain pollution, the European Public Health Alliance (EPHA) reports. The advocacy group uncovered lapses such as dirty production and inadequate waste disposal in the production of antimicrobials in China and I... more
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Guideline for Application to conduct Clinical Trials in Liberia

Liberia Medicines and Health Products Regulatory Authority (LMHRA) (2014) C1
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Indonesia: Buku Data dan Informasi 2016

Pusat Data dan Informasi Kementerian Kesehatan Republik Indonesia (2016) C1
Indonesia's Health Data 2016
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Indonesia Health Profile 2014

Ministry of Health Republic of Indonesia (2015) C1
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Medicines in Health Care Delivery Myanmar

World Health Organization (WHO), Regional Office for South East Asia (2014) C_WHO
Situational Analysis: 13-23 October 2014
Report prepared using the WHO/SEARO workbook tool for undertaking a situational analysis of medicines in health care delivery in low and middle income countries
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Antiretroviral medicines in low- and middle-income countries: Forecasts of global and regional demand for 2014-2018

World Health Organization (2015) C_WHO
Technical Report AIDS Medicines and diagnostics service July 2015
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Landmines, Explosive Remnants of War and IED Safety Handbook (Arabic version)

United Nations Mine Action Service (UNMAS) (2015) C1
Arabic version of the Landmines, ERW and IED Safety Handbook.
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Counterfeit drugs and medical devices in developing countries

Beverly D Glass (2014) CC
The occurrence of a high percentage of couterfeit medicines on the global medicines market is often attributed to a lack of effective regulation and a weak enforcement capacity. This review, while focusing on counterfeit medicines and medical devices in developing countries, will present information... more
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Sierra Leone: GUIDELINES FOR MEDICINAL PRODUCT REGISTRATION

Pharmacy Board of Sierra Leone (PBSR) (2015) C2
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GUIDELINES ON DRUG REGISTRATION APPLICATIONS IN BOTSWANA, 4th edition

Ministry of Health, Gabarone, Botswana (2014)
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WHO good manufacturing practices for pharmaceutical products: main principles

World Health Organization WHO (2014) C_WHO
Licensed pharmaceutical products (marketing authorization) should be manufactured only by licensed manufacturers (holders of a manufacturing authorization) whose activities are regularly inspected by competent national authorities. This guide to GMP shall be used as a standard to justify GMP status,... more
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Pharmaceutical Waste Management An Overview

Kadam. A.; et al. (2016) C1
European Journal of Biomedical and Pharmaceutical Sciences, vol.3 (2016) 1, 192-206 This review shows that if all sub areas of pharmaceutical waste management can efficiently work back to back environmental pollution and dangers to human health can reduce significantly.