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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371 documents on 4 pages
 
 
 
 
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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;


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Essential Medicines for Universal Health Coverage. (Essential Medicines for Universal Health Coverage - Comment. The Lancet Commission on Essential Medicines Policies)

Year:

2016;

Pages:

2;

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Essential Medicines for Universal Health Coverage. (The Lancet Commission on Essential Medicines Policies)

Year:

2016;

Pages:

74;


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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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FIP–WHO Technical Guidelines: Points to Consider in the Provision by Health-care Professionals of Children-specific Preparations That Are Not Available as Authorized Products. WHO Technical Report Series, No. 996, 2016, Annex 2

Year:

2016;

Pages:

24;


Related documents:

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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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General Background Notes on the List of International Comparator Pharmaceutical Products. Who Technical Report Series, No. 1003, 2017, Annex 5

Year:

2017;

Pages:

2;


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

Year:

2014;

Pages:

109;


Countries:

 
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Good Pharmacopoeial Practices. WHO Technical Report Series, No. 996, 2016, Annex 1

Year:

2016;

Pages:

20;


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Guidance on Good Manufacturing Practices: Inspection Report. (Including Appendix 1: Guidance on Good Manufacturing Practices: Inspection Report; Appendix 2: Example of a Risk Category Assessment of the Site Depending on Level of Compliance and Inspection Frequency. WHO Technical Report Series, No. 996, 2016, Annex 4

Year:

2016;

Pages:

16;


Regions:

 
 
 
 
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