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67 documents on 2 pages

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Quality and Safety: Medicines

Quality Assurance

Title:	Access to Medicines and Drug Regulation in Developing Countries: A Resource Guide for DFID
Subjects:	Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support Quality and Safety: Medicines > Safety and Efficacy
Author:	Gray, Andy
Year:	2004 Pages: 16
Publishers:	DFID Health Resource Centre
Regions:	Global

Title:	Act 368 - Sale of Drugs Act 1952 (Revised 1989). Incorporating Latest Amendment - Act A1084/2000
Subjects:	Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
Year:	2000 Pages: 11
Publishers:	Malaysia Ministry of Health, Pharmaceutical Services Division
Countries:	Malaysia

Title:	Analysis of Legal Aspects of Local Pharmaceutical Production in Rwanda
Subjects:	Medicine Access and Rational Use > Supply Management Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
Year:	2006 Pages: 54
Publishers:	German Technical Cooperation Agency (GTZ) / Deutsche Gesellschaft für Technische Zusammenarbeit (GTZ) GmbH
Countries:	Rwanda

Title:	Antimalarial Medicines in Kenya. Availability, Quality and Registration Status. A Baseline Study Undertaken Prior to Nationwide Distribution of Artemether-Lumefantine (AL) in Kenya
Subjects:	Medicine Information and Evidence for Policy > Medicines Policy Quality and Safety: Medicines > Quality Assurance
Year:	2007 Pages: 41
Publishers:	WHO Country Office in Kenya Kenya Ministry of Health Health Action International - Africa
Regions:	EAC East African Community
Countries:	Kenya

Title:	Assessment of Medicine Quality Assurance in Rwanda: Overview of Findings and Recommendations for Consideration. Kigali and Butare, Rwanda, November 9-13, 2009
Subjects:	Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
Author:	Coignez, Veerle; Hajjou, Mustapha; Smine, Abdelkrim
Year:	2009 Pages: 20
Publishers:	United States Pharmacopeia (USP) USAID - Promoting the Quality of Medicines Program (PQM)
Countries:	Rwanda

Title:	Biosimilars. A Unique Opportunity for Iran National Health Sector and National Pharmaceutical Industry
Subjects:	Medicine Information and Evidence for Policy > Medicines Policy Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
Author:	Cheraghali, Abdol Majid
Year:	2012 Pages: 4
Related documents:	Guidelines on Evaluation of Similar Biotherapeutic Products (SBPs). WHO Expert Committee on Biological Standardization, 19-23 October 2009
Related links:	http://www.darujps.com/content/20/1/35
Countries:	Iran (Islamic Republic of)

Title:	Brunei Darussalam Guidelines for Manufacturing and Handling of Halal Medicinal Products, Traditional Medicines and Health Supplements. Guidance Document GD24, First Edition, May 2010
Subjects:	Traditional Medicine > Traditional, Complementary and Herbal Medicine Quality and Safety: Medicines > Quality Assurance
Year:	2010 Pages: 34
Publishers:	The Religious Council Negara Brunei Darussalam
Countries:	Brunei Darussalam

Title:	Combating Counterfeit, Falsified and Substandard Medicines: Defining the Way Forward? Chatham House Briefing Paper, November 2010
Subjects:	Quality and Safety: Medicines > Counterfeit Medicines Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
Author:	Clift, Charles
Year:	2010 Pages: 16
Publishers:	Chatham House (the Royal Institute of International Affairs) - Centre on Global Health Security
Regions:	Global

Title:	Does Price Reveal Poor-quality Drugs? Evidence from 17 Countries
Subjects:	Medicine Access and Rational Use > Pricing Quality and Safety: Medicines > Quality Assurance
Author:	Bate, Roger; Jin, Ginger Zhe; Mathur. Aparna
Year:	2011 Pages: 43
Publishers:	National Bureau of Economic Research, Cambridge, USA
Regions:	Global

Title:	Drug Regulation: History, Present and Future. In: van Boxtel CJ, Santoso B, Edwards IR eds., Drug Benefits and Risks: International Textbook of Clinical Pharmacology, Revised 2nd Ed. (Chapter 6). IOS Press and Uppsala Monitoring Centre, 2008
Subjects:	Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
Author:	Rägo, L; Santoso, Budiono
Year:	2008 Pages: 13
Regions:	Global

Title:	The Drugs (Federal Inspectors, Federal Drug Laboratory and Federal Government Analysts) Rules, 1976 (Pakistan)
Subjects:	Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support Prequalification of Medicines > WHO-UNICEF-UN Project
Year:	1976 Pages: 10
Publishers:	Pakistan Government
Countries:	Pakistan

Title:	Drugs Act, 2035, (1978). Act Number 21 of the Year 2053, 1978 (25 October 1978). An Act Made to Make Provisions Relating to Drugs - Nepal
Subjects:	Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
Year:	1978 Pages: 15
Publishers:	Nepal Government
Countries:	Nepal

Title:	Ensuring the Quality of Medicines in Resource-Limited Countries: An Operational Guide
Subjects:	Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support Quality and Safety: Medicines > Safety and Efficacy
Year:	2007 Pages: 207
Publishers:	United States Agency for International Development (USAID) United States Pharmacopeia (USP)
Regions:	Global

Title:	Exploratory Study on Active Pharmaceutical Ingredient Manufacturing for Essential Medicines
Subjects:	Quality and Safety: Medicines > Quality Assurance
Author:	Betsch, Ekkehard; Bumpas, Janet
Year:	2009 Pages: 52
Publishers:	The World Bank (WB)
Regions:	Global

Title:	FIP Guidelines for the Labels of Prescribed Medicines (2001, Singapore) [French] [Spanish]
Subjects:	Medicine Information and Evidence for Policy > Medicines Policy Medicine Access and Rational Use > Rational Use Quality and Safety: Medicines > Quality Assurance
Year:	2001 Pages: 4
Publishers:	International Pharmaceutical Federation - FIP
Related links:	http://www.fip.org/statements
Regions:	Global

Title:	FIP Statement of Policy on Counterfeit Medicines [French] [Spanish]
Subjects:	Medicine Information and Evidence for Policy > Medicines Policy Quality and Safety: Medicines > Counterfeit Medicines Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
Year:	2003 Pages: 4
Publishers:	International Pharmaceutical Federation - FIP
Related links:	http://www.fip.org/statements
Regions:	Global

Title:	Good Distribution Practices (GDP) for Pharmaceutical Products, 2009 - Egypt
Subjects:	Quality and Safety: Medicines > Quality Assurance
Year:	2009 Pages: 37
Publishers:	Egypt Minister of Health & Population
Countries:	Egypt

Title:	Good Laboratory Practice Regulations, 2008. Nigeria National Agency for Food and Drug Administration and Control (NAFDAC) Act 1993 (as amended)
Subjects:	Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support Quality and Safety: Medicines > Safety and Efficacy
Year:	2008 Pages: 23
Publishers:	Nigeria Ministry of Health - National Agency for Food and Drug Administration and Control (NAFDAC)
Countries:	Nigeria

Title:	Guide to Good Manufacturing Practice for Medicinal Products Part I - PIC/S, PE 009-8 (Part I), 15 January 2009
Subjects:	Quality and Safety: Medicines > Quality Assurance
Year:	2009 Pages: 43
Publishers:	Pharmaceutical Inspection Co-operation Scheme (PIC/S)
Regions:	Global

Title:	Guide to Good Manufacturing Practice for Medicinal Products Part II - PIC/S, PE 009-8 (Part II), 15 January 2009. Developed by the International Conference on Harmonisation (ICH) of Technical Requirements for Registration of Pharmaceuticals for Human Use
Subjects:	Quality and Safety: Medicines > Quality Assurance
Year:	2009 Pages: 55
Publishers:	Pharmaceutical Inspection Co-operation Scheme (PIC/S)
Regions:	Global

Title:	Guideline on Medication Error Reporting, First Edition, July 2009 - Malaysia
Subjects:	Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Safety and Efficacy
Year:	2009 Pages: 30
Publishers:	Malaysia Ministry of Health
Countries:	Malaysia

Title:	Guidelines for Clinical Lab Standards - QASD, MOH Bhutan
Subjects:	Quality and Safety: Medicines > Quality Assurance
Year:	2009 Pages: 84
Publishers:	Bhutan Ministry of Health
Countries:	Bhutan

Title:	Guidelines for Good Clinical Practice (GCP) Inspection. First Edition (Version 1.0), October 2010
Subjects:	Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
Year:	2010 Pages: 46
Publishers:	Malaysia - National Pharmaceutical Control Bureau (NPCB)
Countries:	Malaysia

Title:	Guidelines for Good Distribution Practices for Pharmaceuticals - Kenya. First Edition, June 2006
Subjects:	Medicine Access and Rational Use > Supply Management Quality and Safety: Medicines > Quality Assurance
Year:	2006 Pages: 22
Publishers:	Kenya Ministry of Health - Pharmacy and Poisons Board
Countries:	Kenya

Title:	Guidelines for Importation of Chemicals in Nigeria NAFDAC/NCS/002/00. Directorate of Narcotics and Controlled Substances, Chemical Import Control
Subjects:	Medicine Access and Rational Use > Controlled Medicines Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
Pages:	6
Publishers:	Nigeria Ministry of Health - National Agency for Food and Drug Administration and Control (NAFDAC)
Countries:	Nigeria

Title:	Guidelines on GMP Inspection of Foreign Pharmaceutical Manufacturing Plants Use in Uganda, February 2007 - National Drug Authority, Uganda
Subjects:	Quality and Safety: Medicines > Quality Assurance
Year:	2007 Pages: 5
Publishers:	Uganda - National Drug Authority (NDA), Ministry of Health
Related links:	http://www.nda.or.ug/drug-insp.php
Countries:	Uganda

Title:	Handbook: Good Laboratory Practice (GLP). Quality Practices for Regulated Non-clinical Research and Development - 2nd Ed.
Subjects:	Quality and Safety: Medicines > Quality Assurance Prequalification of Medicines > WHO-UNICEF-UN Project
Year:	2009 Pages: 328
Publishers:	WHO/TDR - World Health Organization Special Programme for Research and Training in Tropical Diseases WHO Headquarters in Geneva The World Bank (WB) United Nations Children's Fund (UNICEF) United Nations Development Programme (UNDP)
Related documents:	Handbook: Non-Clinical Safety Testing
Regions:	Global

Title:	The Importance of Medicines Safety - Southern Med Review Vol 5 Issue 1 July 2012
Subjects:	Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Safety and Efficacy
Author:	Kiani, Ayyaz
Year:	2012 Pages: 2
Publishers:	Southern Med Review
Related links:	http://southernmedreview.org
Regions:	Global

Title:	Instability of (Methyl) Ergometrine in Tropical Climates: An Overview. European Journal of Obstetrics & Gynecology and Reproductive Biology 69 (1996) 25-29
Subjects:	Medicine Access and Rational Use > Supply Management Quality and Safety: Medicines > Quality Assurance
Author:	Hogerzeil, Hans V; Walker, Godfrey J.A.
Year:	1996 Pages: 5
Regions:	Global

Title:	Jan Aushadhi Stores in India and Quality of Medicines Therein
Subjects:	Medicine Access and Rational Use > Pricing Quality and Safety: Medicines > Quality Assurance
Author:	Kotwani, Anita; Nanda, Arun; Singal, G.L.
Year:	2011 Pages: 4
Countries:	India

Title:	Malaysian Guidelines for Good Clinical Practice
Subjects:	Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Safety and Efficacy
Year:	2004 Pages: 88
Publishers:	Malaysia Ministry of Health
Countries:	Malaysia

Title:	Malaysian Guidelines for the Conduct of Bioavailability and Bioequivalence Studies, 2000
Subjects:	Quality and Safety: Medicines > Quality Assurance
Year:	2000 Pages: 28
Publishers:	Malaysia Ministry of Health
Countries:	Malaysia

Title:	MDS-3: Managing Access to Medicines and Health Technologies (Third Edition)
Subjects:	Medicine Information and Evidence for Policy > Medicines Policy Medicine Access and Rational Use > Financing Medicine Access and Rational Use > Pricing Medicine Access and Rational Use > Rational Use Medicine Access and Rational Use > Selection Medicine Access and Rational Use > Supply Management Traditional Medicine > Traditional, Complementary and Herbal Medicine Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
Year:	2012 Pages: 1088
Publishers:	Management Sciences for Health (MSH)
Related documents:	Toward Sustainable Access to Medicines. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 1) Historical and Institutional Perspectives. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 2) Intellectual Property and Access to Medicines. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 3) National Medicine Policy. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 4) Traditional and Complementary Medicine Policy. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 5) Pharmaceutical Legislation and Regulation. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 6) Pharmaceutical Production Policy. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 7) Pharmaceutical Pricing Policy. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 9) Economics for Pharmaceutical Management. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 10) Pharmaceutical Financing Strategies. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 11) Pharmaceutical Benefits in Insurance Program. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 12) Revolving Drug Funds and User Fees. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 13) Global and Donor Financing. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 14) Pharmaceutical Donations. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 15) Managing Medicine Selection. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 16) Treatment Guidelines and Formulary Manuals. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 17) Pharmaceutical Supply Strategies. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 8) Managing Procurement. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 18) Quality Assurance for Pharmaceuticals. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 19) Quantifying Pharmaceutical Requirements. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 20) Managing the Tender Process. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 21) Managing Distribution. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 22) Inventory Management. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 23) Importation and Port Clearing. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 24) Transport Management. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 25) Kit System Management. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 26) Managing for Rational Medicine Use. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 27) Investigating Medicine Use. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 28) Promoting Rational Prescribing. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 29) Ensuring Good Dispensing Practices. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 30) Community-Based Participation and Initiatives. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 31) Drug Seller Initiatives. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 32) Encouraging Appropriate Medicine Use by Consumers. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 33) Medicine and Therapeutics Information. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 34) Pharmacovigilance. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 35) Pharmaceutical Supply Systems Assessment. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 36) Managing Pharmaceutical Programs. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 37) Planning for Pharmaceutical Management. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 38) Contracting for Pharmaceuticals and Services. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 39) Analyzing and Controlling Pharmaceutical Expenditures. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 40) Financial Planning and Management. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 41) Planning and Building Storage Facilities. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 42) Security Management. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 43) Medical Stores Management. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 44) Hospital Pharmacy Management. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 45) Pharmaceutical Management for Health Facilities. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 46) Laboratory Services and Medical Supplies. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 47) Monitoring and Evaluation. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 48) Pharmaceutical Management Information Systems. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 49) Computers in Pharmaceutical Management. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 50) Human Resources Management and Capacity Development. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 51) Designing and Implementing Training Programs. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 52) MDS-3: Managing Access to Medicines and Health Technologies. Front Matter, including Contributors, Reviewers, Contents, and How to Use MDS-3 MDS-3: Managing Access to Medicines and Health Technologies. Index
Related links:	http://www.msh.org/resource-center/managing-drug-supply.cfm
Regions:	Global

Title:	MHLW Ministerial Ordinance No. 136, 2004. Ministerial Ordinance on Standards for Quality for Drugs, Quasi-drugs, Cosmetics and Medical Devices - Japan
Subjects:	Medicine Information and Evidence for Policy > Information and Publications Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
Year:	2004 Pages: 16
Publishers:	Japan - Ministry of Health, Labour and Welfare (MHLW)
Countries:	Japan

Title:	MHLW Ministerial Ordinance No. 179, 2004. Ministerial Ordinance on Standards for Manufacuring Control and Quality Control for Drugs and Quasi-drugs.
Subjects:	Medicine Information and Evidence for Policy > Information and Publications Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
Year:	2004 Pages: 23
Publishers:	Japan - Ministry of Health, Labour and Welfare (MHLW)
Countries:	Japan

Title:	Myths, Questions, Facts About Generic Drugs in the EU
Subjects:	Medicine Information and Evidence for Policy > Medicines Policy Medicine Access and Rational Use > Pricing Quality and Safety: Medicines > Quality Assurance
Author:	Baumgärtel, Christoph
Year:	2012 Pages: 5
Regions:	Europe (EURO)

Title:	National Pharmaceutical Control Bureau, Annual Report 2009 - Malaysia
Subjects:	Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support Quality and Safety: Medicines > Safety and Efficacy
Year:	2010 Pages: 97
Publishers:	Malaysia - National Pharmaceutical Control Bureau (NPCB)
Countries:	Malaysia

Title:	PhAMA Code of Conduct for Non Prescription (OTC) Products - Malaysia
Subjects:	Medicine Access and Rational Use > Rational Use Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Safety and Efficacy
Year:	2008 Pages: 7
Publishers:	Pharmaceutical Association of Malaysia (PhAMA) / Persatuan Farmaseutikal Malaysia
Countries:	Malaysia

Title:	Pharmaceuticals: Counterfeits, Sustandard Drugs and Drug Diversion. World Bank, HNP Brief #2
Subjects:	Quality and Safety: Medicines > Counterfeit Medicines Quality and Safety: Medicines > Quality Assurance
Author:	Seiter, Andreas
Year:	2005 Pages: 4
Publishers:	The World Bank (WB)
Regions:	Global

Title:	Pharmaceuticals: Drug Regulation in Low and Middle Income Countries. World Bank, HNP Brief #4
Subjects:	Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
Author:	Seiter, Andreas
Year:	2005 Pages: 4
Publishers:	The World Bank (WB)
Regions:	Global

Title:	Pharmaceuticals: Local Manufacturing. World Bank, HNP Brief #3
Subjects:	Medicine Access and Rational Use > Supply Management Quality and Safety: Medicines > Quality Assurance
Author:	Seiter, Andreas
Year:	2005 Pages: 5
Publishers:	The World Bank (WB)
Regions:	Global

Title:	Pharmaceuticals: Quality Assurance in the Distribution Chain. World Bank, HNP Brief #6
Subjects:	Medicine Access and Rational Use > Supply Management Quality and Safety: Medicines > Quality Assurance
Author:	Seiter, Andreas
Year:	2005 Pages: 5
Publishers:	The World Bank (WB)
Regions:	Global

Title:	Pharmalink Newsletter, Vol 10, Issue 1, October 2010. Assuring the Quality of Medicines [French]
Subjects:	Medicine Information and Evidence for Policy > Information and Publications Quality and Safety: Medicines > Quality Assurance Prequalification of Medicines > WHO-UNICEF-UN Project
Author:	Bonsmann, Christoph; Haefele-Abah, Christine; Liedtke, Christine; Lwanyaga, Joanita N.; Mohanta, Guru Prasad; Mubangizi, Deusdedit; Nandama, Wycliffe
Year:	2010 Pages: 16
Related links:	http://www.epnetwork.org/
Regions:	Global

Title:	A Poor-quality Generic Drug for the Treatment of Visceral Leishmaniasis: A Case Report and Appeal
Subjects:	Medicine Access and Rational Use > Supply Management Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support Quality and Safety: Medicines > Safety and Efficacy
Author:	Beijnen, Jos H.; de Vries, Peter J.; Dorlo, Thomas P. C.; Eggelte, Teunis A.; Schoone, Gerard J.
Year:	2012 Pages: 4
Regions:	Global
Countries:	Bangladesh

Title:	Potency of Ergometrine in Tropical Countries
Subjects:	Medicine Access and Rational Use > Supply Management Quality and Safety: Medicines > Quality Assurance
Author:	Hillgren, Ulf; Hogerzeil, Hans V; Walker, Godfrey J.A.
Year:	1988 Pages: 1
Related documents:	The Quality and Stability of Essential Drugs in Rural Zimbabwe: Controlled Longitudinal Study
Regions:	Global

Title:	Pre Qualification of Suppliers of Pharmaceuticals and Medical Devices-State Pharmaceuticals Corporation (National Procurement Agency, Sri Lanka)
Subjects:	Medicine Access and Rational Use > Supply Management Quality and Safety: Medicines > Quality Assurance Prequalification of Medicines > WHO-UNICEF-UN Project
Year:	2007 Pages: 1
Publishers:	Sri Lanka Ministry of Healthcare and Nutrition
Countries:	Sri Lanka

Title:	Public and Private Sector Approaches to Improving Pharmaceutical Quality in Bangladesh - Bangladesh Development Series Paper No. 23
Subjects:	Medicine Access and Rational Use > Pricing Quality and Safety: Medicines > Quality Assurance
Year:	2008 Pages: 62
Publishers:	The World Bank (WB)
Countries:	Bangladesh

Title:	Putting Contract Research Organisations on the Radar. An Exploratory Study on the Outsourcing of Clinical Trials by Pharmaceutical Companies to Contract Research Organisations in Non-Traditional Trial Regions
Subjects:	Quality and Safety: Medicines > Quality Assurance
Author:	Balbinot, Rachelle Amalia Agostini; Bhagianadh, Divya; da Freitas, Corina Bontempo Duca; Dallari,S ueli Gandolfi; Delgado, Duilio Jesús Fuentes; Homedes, Núria; Martich, Evangelina; Martínez, Gabriela Minaya; Schipper, Irene; Ugalde, Antonio; van Huijstee, Mariëtte
Year:	2011 Pages: 103
Publishers:	Centre for Studies in Ethics and Rights - CSER Salud y Fármacos Stichting Onderzoek Multinationale Ondernemingen (SOMO) / Centre for Research on Multinational Corporations
Regions:	Global; America (AMRO)
Countries:	Argentina; Brazil; Peru; India

Title:	The Quality and Stability of Essential Drugs in Rural Zimbabwe: Controlled Longitudinal Study
Subjects:	Medicine Access and Rational Use > Supply Management Quality and Safety: Medicines > Quality Assurance
Author:	Hogerzeil, Hans V; Nazerali, Hanif
Year:	1998 Pages: 3
Related documents:	Potency of Ergometrine in Tropical Countries
Related links:	www.bmj.com
Countries:	Zimbabwe

Title:	Quality Assurance for Pharmaceuticals. (MDS-3: Managing Access to Medicines and Health Technologies, Chapter 19)
Subjects:	Medicine Information and Evidence for Policy > Medicines Policy Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support Prequalification of Medicines > WHO-UNICEF-UN Project
Author:	Layloff, Thomas
Year:	2012 Pages: 23
Publishers:	Management Sciences for Health (MSH)
Related documents:	MDS-3: Managing Access to Medicines and Health Technologies (Third Edition)
Related links:	http://www.msh.org/resource-center/mds-3-digital-edition.cfm
Regions:	Global


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Last updated: May 3, 2013