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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191 documents on 2 pages
 
 
 
 
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Multisource (Generic) Pharmaceutical Products: Guidelines on Registration Requirements to Establish Interchangeability. Republication of Multisource (Generic) Pharmaceutical Products: Guidelines on Registration Requirements to Establish Interchangeability, WHO Technical Report Series, No. 992, Annex 7 with a New Appendix 2. WHO Technical Report Series, No. 1003, 2017, Annex 6

Year:

2017;

Pages:

56;


Regions:

 
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Placebo and Drug Kits in Clinical Trial Design. (Who Drug Information Vol. 31, No. 2, 2017)

Year:

2017;

Pages:

4;


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Prequalification of Quality Control Laboratories: Procedure for Assessing the Acceptability, in Principle, of Quality Control Laboratories for Use by United Nations Agencies. Who Technical Report Series No. 1003, 2017, Annex 3

Year:

2017;

Pages:

12;


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A Quiet Revolution in Global Public Health: The World Health Organization’s Prequalification of Medicines Programme

Year:

2014;

Pages:

25;

Regions:

 
 
 
 
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