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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403 documents on 5 pages
 
 
 
 
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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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Development of a Risk-Based Approach and Tools for Improving Safe and Rational Use of Tuberculosis Medicines

Year:

2013;

Pages:

40;


Regions:

 
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Documento de Autoevaluación de Buenas Prácticas de Laboratorio (BPL) / Documento de Auto-Avaliação de Boas Práticas de Laboratório (BPL) / Document on Self-Evaluation of Good Laboratory Practices (GLP) - Red PARF Documento Técnico No. 6 (Red Panamericana de Armonización de la Reglamentación Farmacéutica)

Year:

2011;

Pages:

113;


 
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Emergency Use Assessment and Listing Procedure (EUAL) for Candidate in Vitro Diagnostics (IVDs) for Use in the Context of a Public Health Emergency

Year:

2015;

Pages:

11;


Regions:

 
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Emergency Use Assessment and Listing Procedure (EUAL) for Candidate Medicines for Use in the Context of a Public Health Emergency

Year:

2015;

Pages:

9;


Regions:

 
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Emergency Use Assessment and Listing Procedure (EUAL) for Candidate Vaccines for Use in the Context of a Public Health Emergency

Year:

2015;

Pages:

10;


Regions:

 
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Estudio sobre las Condiciones Actuales de los Laboratorios Oficiales de Control de Calidad de Medicamentos (LOCM) en América Latina y el Caribe / World Health Organization (WHO) Study of the Current Conditions of the Official Medicine Control Laboratories (OMCL) in Latin America and the Caribbean / Estudo sobre as Condições Atuais dos Laboratórios Oficiais de Controle da Qualidade de Medicamentos (LOCM) na América Latina e Caribe Farmacêutico - Red PARF Documento Técnico No. 4 (Red Panamericana de Armonización de la Reglamentación Farmacéutica)

Year:

2010;

Pages:

45;


 
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Framework for Implementation of Equivalence Requirements for Pharmaceutical Products - PANDRH Technical Report Nº8 (Pan American Network for Drug Regulatory Harmonization) [Spanish]

Year:

2011;

Pages:

38;


 
 
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Good Manufacturing Practice Guideline for Pharmaceutical Products: Main Principles. First Edition, 2014 - Ethiopia

Year:

2014;

Pages:

109;


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Countries:

 
 
 
 
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