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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519 documents on 7 pages
 
 
 
 
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MOH Guidelines on Submission of Documentation for Registration of Human Pharmaceutical Products. First Edition, 2014 - Republic of Rwanda

Year:

2014;

Pages:

436;


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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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National Drug Law - Union of Myanmar. (The State Law and Order Restoration Council Law No. 7/92. The 5th Waning Day of Tazaungmon, 1354 M.E. 30th October, 1992)

Year:

1992;

Pages:

9;


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National Drug Regulatory Legislation: Guiding Principles for Small Drug Regulatory Authorities. WHO Technical Report Series, No. 885, 1999, Annex 8 [Spanish]

Year:

1999;

Pages:

41;


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National Medicines Regulatory Authority Act, No. 5 of 2015. (Published as a Supplement to Part II of the Gazette of the Democratic Socialist Republic of Sri Lanka of March 20, 2015)

Year:

2015;

Pages:

98;


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Pharmaceutical Regulation in 15 European Countries: Review. Health Systems in Transition, 2016; 18(5):1–118

Year:

2016;

Pages:

143;


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Première Conférence Scientifique Biennale sur la Réglementation des Médicaments en Afrique. Johannesburg, Afrique du Sud, 2-3 Décembre 2013 - Livre des Résumés. Thème de la Conférence : Établir des Partenariats pour le Renforcement Durable des Capacités dans la Réglementation des Médicaments en Afrique [English]

Year:

2013;

Pages:

70;


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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;


Regions:

 
 
 
 
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