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.
Expand the sub-collections menu.
493 documents on 5 pages
 
 
 
 
 
Open this document and view its content

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

Year:

2014;

Pages:

109;


Countries:

 
Open this document and view its content

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

Year:

2016;

Pages:

20;


Regions:

 
Open this document and view its content

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:

 
Open this document and view its content

A Guide to Aid the Selection of Diagnostic Tests. (Bull World Health Organ 2017;95:639–645)

Year:

2017;

Pages:

7;


Related documents:

Regions:

 
Open this document and view its content

Guideline for Good Clinical Practice. ICH Harmonised Tripartite Guideline. E6(R1). Current Step 4 version, dated 10 June 1996. (including the Post Step 4 corrections). The International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH).

Year:

1996;

Pages:

59;


 
Open this document and view its content

Guideline for Good Storage Practices, Good Distribution Practice, and Pharmaceutical Product Recall. First Edition, September 2015 - Ethiopia

Year:

2015;

Pages:

71;


Countries:

 
Open this document and view its content

Guideline for Registration of Medicines. Third Edition, June 2014 - Ethiopia

Year:

2014;

Pages:

141;


Countries:

 
Open this document and view its content

Guidelines for Conducting Clinical Trials - Sierra Leone

Year:

2013;

Pages:

14;


Countries:

 
Open this document and view its content

Guidelines for Conducting Clinical Trials of Medicines, Food Supplements, Vaccines and Medical Devices in Sierra Leone

Year:

2014;

Pages:

32;


Countries:

 
Open this document and view its content

Guidelines for Medicinal Product Registration - Sierra Leone

Year:

2013;

Pages:

28;


Related documents:

Countries:

 
 
 
 
The WHO Essential Medicines and Health Products Information Portal was designed and is maintained by Human Info NGO. Last updated: November 7, 2017