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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400 documents on 4 pages
 
 
 
 
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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;


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

Year:

2017;

Pages:

7;


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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;


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

Year:

2015;

Pages:

71;


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

Year:

2014;

Pages:

141;


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Guidelines for Conducting Clinical Trials - Sierra Leone

Year:

2013;

Pages:

14;


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

Year:

2014;

Pages:

32;


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Guidelines for Medicinal Product Registration - Sierra Leone

Year:

2013;

Pages:

28;


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Guidelines for the Production, Control and Regulation of Snake Antivenom Immunoglobulins. Replacement of Annex 2 of Who Technical Report Series, No. 964. Who Expert Committee on Biological Standardization, Sixty-seventh Report; Who Technical Report Series No. 1004, 2017, Annex 5

Year:

2017;

Pages:

192;


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Guidelines on Import Procedures for Pharmaceutical Products. WHO Technical Report Series, No. 863, 1996, Annex 12 (with Appendix: Special Import Controls for Narcotic Drugs and Psychotropic Substances)

Year:

2014;

Pages:

10;


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Guidelines on Regulatory Preparedness for Provision of Marketing Authorization of Human Pandemic Influenza Vaccines in Non-vaccine-producing Countries. Who Expert Committee on Biological Standardization, Sixty-seventh Report; Who Technical Report Series No. 1004, 2017, Annex 7

Year:

2017;

Pages:

29;


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Guidelines on Submission of Documentation for a Multisource (Generic) Finished Pharmaceutical Product for the WHO Prequalification of Medicines Programme: Quality Part. WHO Technical Report Series, No. 970, 2012, Annex 4

Year:

2012;

Pages:

76;


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Guidelines on the Conduct of Surveys of the Quality of Medicines. WHO Technical Report Series, No. 996, 2016, Annex 7

Year:

2016;

Pages:

36;


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