Regions

The following classification of the documents is based on the geographical region to which these documents refer/apply to. Publications are available in HTML, PDF , DOC or XLS format. Click on the corresponding icon to open the publication.
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154 documents on 4 pages
 
 
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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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Caribbean Pharmaceutical Policy (Approved April 2011)

Year:

2013;

Pages:

73;


 
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Criterios éticos para la promoción, propaganda y publicidad de medicamentos - Red PARF Documento Técnico Nº 12 (Red Panamericana de Armonización de la Reglamentación Farmacéutica) [English] [French]

Year:

2013;

Pages:

16;


 
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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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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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Ethical Criteria for the Promotion, Advertisement, and Publicity of Medicines - PANDRH Series Technical Document No 12 (Pan American Network for Drug Regulatory Harmonization) [French] [Spanish]

Year:

2013;

Pages:

14;


 
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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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