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Quality and Safety: Medicines

Quality Assurance

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Titre:	13th International Conference of Drug Regulatory Authorities (ICDRA) Berne, Switzerland, 16-19 September 2008. ICDRA: Medicines Agencies Decide Future Action
Sujets:	Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
An:	2008 Pages: 19
Éditeurs:	WHO Headquarters in Geneva
Liens associés:	http://www.who.int/medicines/areas/quality_safety/regulation_legislation/icdra/en/index.html
Régions:	Global

Titre:	14th International Conference of Drug Regulatory Authorities(ICDRA), Singapore 30 November - 3 December 2010
Sujets:	Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
An:	2011 Pages: 16
Éditeurs:	WHO Headquarters in Geneva
Liens associés:	http://www.who.int/medicines/areas/quality_safety/regulation_legislation/icdra/en/index.html

Titre:	Accelerated Stability Studies of Widely Used Pharmaceutical Substances Under Simulated Tropical Conditions
Sujets:	Quality and Safety: Medicines > Quality Assurance
An:	1986 Pages: 119
Éditeurs:	WHO Headquarters in Geneva
Régions:	Global

Titre:	Access to Medicines and Drug Regulation in Developing Countries: A Resource Guide for DFID
Sujets:	Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support Quality and Safety: Medicines > Safety and Efficacy
Auteur:	Gray, Andy
An:	2004 Pages: 16
Éditeurs:	DFID Health Resource Centre
Régions:	Global

Titre:	Act 368 - Sale of Drugs Act 1952 (Revised 1989). Incorporating Latest Amendment - Act A1084/2000
Sujets:	Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
An:	2000 Pages: 11
Éditeurs:	Malaysia Ministry of Health, Pharmaceutical Services Division
Pays:	Malaisie

Titre:	Additional Guidance for Organizations Performing in Vivo Bioequivalence Studies. WHO Technical Report Series, No. 937, 2006, Annex 9
Sujets:	Quality and Safety: Medicines > Quality Assurance Prequalification of Medicines > WHO-UNICEF-UN Project
An:	2006 Pages: 23
Éditeurs:	WHO Headquarters in Geneva
Documents similaires:	WHO Expert Committee on Selection and Use of Essential Medicines - WHO Technical Report Series, No. 850, Annex 3 (Guidelines for Good Clinical Practice (GCP) for Trials on Pharmaceutical Products) - Sixth Report Proposal to Waive in Vivo Bioequivalence Requirements for WHO Model List of Essential Medicines Immediate-release, Solid Oral Dosage Forms. WHO Technical Report Series, No. 937, 2006, Annex 8
Régions:	Global

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

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

Titre:	Application of Hazard Analysis and Critical Control Point (HACCP) Methodology to Pharmaceuticals. WHO Technical Report Series, No. 908, 2003, Annex 7
Sujets:	Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
An:	2003 Pages: 14
Éditeurs:	WHO Headquarters in Geneva
Régions:	Global

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

Titre:	Basic Tests for Drugs - Pharmaceutical Substances, Medicinal Plant Materials and Dosage Forms [French] [Spanish]
Sujets:	Quality and Safety: Medicines > Quality Assurance
An:	1998 Pages: 100
Éditeurs:	WHO Headquarters in Geneva
Régions:	Global

Titre:	Basic Tests for Pharmaceutical Substances [French] [Spanish]
Sujets:	Quality and Safety: Medicines > Quality Assurance
An:	1986 Pages: 216
Éditeurs:	WHO Headquarters in Geneva
Régions:	Global

Titre:	Biosimilars. A Unique Opportunity for Iran National Health Sector and National Pharmaceutical Industry
Sujets:	Medicine Information and Evidence for Policy > Medicines Policy Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
Auteur:	Cheraghali, Abdol Majid
An:	2012 Pages: 4
Documents similaires:	Guidelines on Evaluation of Similar Biotherapeutic Products (SBPs). WHO Expert Committee on Biological Standardization, 19-23 October 2009
Liens associés:	http://www.darujps.com/content/20/1/35
Pays:	Iran (République islamique d')

Titre:	Brunei Darussalam Guidelines for Manufacturing and Handling of Halal Medicinal Products, Traditional Medicines and Health Supplements. Guidance Document GD24, First Edition, May 2010
Sujets:	Traditional Medicine > Traditional, Complementary and Herbal Medicine Quality and Safety: Medicines > Quality Assurance
An:	2010 Pages: 34
Éditeurs:	The Religious Council Negara Brunei Darussalam
Pays:	Brunéi Darussalam

Titre:	Combating Counterfeit, Falsified and Substandard Medicines: Defining the Way Forward? Chatham House Briefing Paper, November 2010
Sujets:	Quality and Safety: Medicines > Counterfeit Medicines Quality and Safety: Medicines > Quality Assurance Quality and Safety: Medicines > Regulatory Support
Auteur:	Clift, Charles
An:	2010 Pages: 16
Éditeurs:	Chatham House (the Royal Institute of International Affairs) - Centre on Global Health Security
Régions:	Global

Titre:	Considerations for Requesting Analysis of Drug Samples. WHO Technical Report Series, No. 902, 2002, Annex 4
Sujets:	Quality and Safety: Medicines > Quality Assurance
An:	2002 Pages: 4
Éditeurs:	WHO Headquarters in Geneva
Documents similaires:	Model Certificate of Analysis. WHO Technical Report Series, No. 902, 2002, Annex 10
Régions:	Global

Titre:	Development of Paediatric Medicines: Points to Consider in Formulation. WHO Technical Report Series, No. 970, 2012, Annex 5
Sujets:	Quality and Safety: Medicines > Quality Assurance
An:	2012 Pages: 29
Éditeurs:	WHO Headquarters in Geneva
Documents similaires:	WHO Expert Committee on Specifications for Pharmaceutical Preparations - WHO Technical Report Series, No. 970 - Forty-sixth Report (Geneva, 10–14 October 2011)
Liens associés:	http://www.who.int/medicines/areas/quality_safety/quality_assurance/guidelines/en/index.html http://www.who.int/childmedicines/en/
Régions:	Global

Titre:	Does Price Reveal Poor-quality Drugs? Evidence from 17 Countries
Sujets:	Medicine Access and Rational Use > Pricing Quality and Safety: Medicines > Quality Assurance
Auteur:	Bate, Roger; Jin, Ginger Zhe; Mathur. Aparna
An:	2011 Pages: 43
Éditeurs:	National Bureau of Economic Research, Cambridge, USA
Régions:	Global

Titre:	Drug Quality Control Laboratories
Sujets:	Quality and Safety: Medicines > Quality Assurance
An:	1999 Pages: 42
Éditeurs:	World Health Organization - Regional Office for Africa (WHO/AFRO)
Documents similaires:	Report of a Meeting on the Optimal Use of Regional Drug Quality Control Laboratories in Africa
Régions:	Afrique (AFRO)

Titre:	Drug Quality Screening in Developing Countries: Establishment of an Appropriate Laboratory in Swaziland
Sujets:	Quality and Safety: Medicines > Quality Assurance
Auteur:	Kenyon, A.S.; Kenyon, T.A.; Sibiya, T.
An:	1994 Pages: 6
Éditeurs:	WHO Headquarters in Geneva
Pays:	Swaziland


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Dernière mise à jour: le 3 mai 2013