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On this page readers can obtain a listing of documents classified by keywords. Click on the bookshelf icon of a keyword to obtain the concerned documents or to return to the main list of keywords.
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138 documents on 3 pages
 
 
 
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Antimicrobial Resistance: What Does Medicine Quality Have to Do with It?

Year:

2015;

Pages:

45;

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Building Clinical Trial Capacity to Develop a New Treatment for Multidrug-resistant Tuberculosis. (Bull World Health Organ 2016;94:147–152)

Year:

2016;

Pages:

6;


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Building Clinical Trials Capacity for Tuberculosis Drugs in High-Burden Countries

Year:

2007;

Pages:

4;

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Compendium of Good Manufacturing Practices (GMP) Technical Documents for Harmonization of Medicines Regulation in The East African Community, 2014

Year:

2014;

Pages:

336;


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Concept paper for discussion: A stepwise approach for pharmaceutical companies in developing countries to attain WHO GMP standards. (WHO Drug Information Vol. 30, No. 2, 2016)

Year:

2016;

Pages:

13;


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Cuban Experience with Local Production of Medicines, Technology Transfer and Improving Access to Health [Spanish]

Year:

2015;

Pages:

76;


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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;


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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;


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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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Experiencia cubana en la producción local de medicamentos, transferencia de tecnología y mejoramiento en el acceso a la salud [English]

Year:

2015;

Pages:

80;


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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;


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

Year:

2014;

Pages:

109;


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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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Guidance on the Selection of Comparator Pharmaceutical Products for Equivalence Assessment of Interchangeable Multisource (Generic) Products. WHO Technical Report Series, No. 992, 2015, Annex 8

Year:

2015;

Pages:

6;


Regions:

 
 
 
 
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