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.
120 documents on 3 pages
 
 
 
 
Open this document and view its content

Adverse Event Reporting on Antiretroviral Medicines in KwaZulu-Natal for April 2007 to March 2012

Year:

2014;

Pages:

50;


Related documents:

Countries:

 
Open this document and view its content

Antiretroviral Cohort Adverse Event Monitoring In Kwazulu-Natal, April 2014

Year:

2014;

Pages:

110;


Countries:

 
Open this document and view its content

Assessment of the Regulatory Systems and Capacity of the Directorate General for Drug Administration in Bangladesh

Year:

2012;

Pages:

73;


Countries:

 
Open this document and view its content

Clinical Trials Have Gone Global: Is This a Good Thing?

Year:

2012;

Pages:

5;

Related documents:

Regions:

 
Open this document and view its content

Comprehensive Assessment of Pharmacovigilance Systems and their Performance in Sub-Saharan Africa

Year:

2012;

Pages:

1;


 
Open this document and view its content

Designing a National Combined Reporting Form for Adverse Drug Reactions and Medication Errors - Malta

Year:

2015;

Pages:

10;

Countries:

 
Open this document and view its content

Development of a Risk-Based Approach and Tools for Improving Safe and Rational Use of Tuberculosis Medicines

Year:

2013;

Pages:

40;


Regions:

 
Open this document and view its content

Governance and Pharmacovigilance in Brazil: A Scoping Review

Year:

2016;

Pages:

15;

Countries:

 
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

Health Professionals' Knowledge, Attitudes and Practices about Pharmacovigilance in India: A Systematic Review and Meta-Analysis

Year:

2016;

Pages:

15;

Related documents:

Countries:

 
 
 
 
The WHO Essential Medicines and Health Products Information Portal was designed and is maintained by Human Info NGO. Last updated: November 2, 2016