Subjects

On this page readers can obtain a listing of documents under the subject headings. Click on the name of a subject heading to display the sub-headings, or to return to the main subjects. Click on the icon of a sub-heading to obtain the concerned documents. Publications are available in HTML, PDF , DOC or XLS format. Click on the corresponding icon to open the publication. The PDF icon located on the cover page of a publication represents that the publication is available only in PDF format. If the PDF icon is located near the title of the publication it means the document is available in both HTML and PDF formats.
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442 documents on 9 pages
 
 
 
 
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Addressing the Barriers to Effective Monitoring, Reporting and Containment of Spurious/Substandard/Falsely-labelled/ Falsified/Counterfeit Medical Products through Sustainable Multi-stakeholder Collaboration and Community/Consumer-based Interventions. A report prepared for the Medicines Transparency Alliance, Philippines

Year:

2016;

Pages:

94;


Countries:

 
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Analysis of the Regulatory Capacity to Assure the Quality of Antimalarial Medicines in Selected Countries of the Greater Mekong Subregion of Asia. March 2015

Year:

2015;

Pages:

110;


 
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Antimicrobial Resistance: What Does Medicine Quality Have to Do with It?

Year:

2015;

Pages:

45;

Regions:

 
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Assessment of the Regulatory Systems and Capacity of the Directorate General for Drug Administration in Bangladesh

Year:

2012;

Pages:

73;


Countries:

 
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Boas Práticas da OMS para Laboratórios de Controle de Qualidade de Produtos Farmacêuticos (Série de Relatórios Tecnicos da OMS, No. 957, 2010 - Relatório 44, Anexo 1) e Documento de Auto-Avaliação de Boas Práticas de Laboratório (BPL) - Rede PARF Documento Técnico No. 9 (Rede Pan-Americana da Harmonização de Regulamentação Farmacêutica) [English] [French] [Spanish] [Thai]

Year:

2011;

Pages:

58;


 
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Boas práticas da OMS para laboratórios de microbiologia farmacêutica - Rede PARF Documento Técnico Nº 11 (Rede Pan-Americana da Harmonização de Regulamentação Farmacêutica) [English]

Year:

2012;

Pages:

37;


 
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Building Clinical Trial Capacity to Develop a New Treatment for Multidrug-resistant Tuberculosis. (Bull World Health Organ 2016;94:147–152)

Year:

2016;

Pages:

6;


Regions:

 
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Building Clinical Trials Capacity for Tuberculosis Drugs in High-Burden Countries

Year:

2007;

Pages:

4;

Regions:

 
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Clinical Trials Have Gone Global: Is This a Good Thing?

Year:

2012;

Pages:

5;

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Collaborative Procedure Between the World Health Organization (WHO) Prequalification Team and National Regulatory Authorities in the Assessment and Accelerated National Registration of WHO-prequalified Pharmaceutical Products and Vaccines. WHO Technical Report Series, No. 996, 2016, Annex 8

Year:

2016;

Pages:

42;


Regions:

 
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Compendium of Good Manufacturing Practices (GMP) Technical Documents for Harmonization of Medicines Regulation in The East African Community, 2014

Year:

2014;

Pages:

336;


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