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WHO Expert Committee on specifications for pharmaceutical preparations.

dc.contributor.authorBawazir, SA
dc.contributor.authorCaudron, JM
dc.contributor.authorDekker, TG
dc.contributor.authorGuerrero Rivas, NM
dc.contributor.authorHoogmartens, J
dc.contributor.authorShaohong, J
dc.contributor.authorMiller, JH
dc.contributor.authorMolzon, JA
dc.contributor.authorTreebamroog, M
dc.contributor.authorBiwota, EW
dc.contributor.authorAddae-Mensah, I
dc.contributor.authorKristensen, HG
dc.contributor.authorRabouhans, ML
dc.contributor.authorRobert, JL
dc.contributor.authorSingh, S
dc.contributor.authorTribe, R
dc.contributor.authorFarquharson, GJ
dc.contributor.authorMills, S
dc.contributor.authorPelkonen, E
dc.contributor.authorSchumauser, B
dc.contributor.authorSmith, D
dc.contributor.authorSpeitzhofer, A
dc.contributor.authorJakobsen, PS
dc.contributor.authorDaviaud, J
dc.contributor.authorLodi, A
dc.contributor.authorKozarewicz, P
dc.contributor.authorBeatrice, MG
dc.contributor.authorCappuccino, N
dc.contributor.authorSuffolk, B
dc.contributor.authorHoek, AJ
dc.contributor.authorAnquez-Traxler, C
dc.contributor.authorFitzGerald, M
dc.contributor.authorVallender, M
dc.contributor.authorKim, HS
dc.contributor.authorLee, SJ
dc.contributor.authorRusso, KA
dc.contributor.authorEtienne, CF
dc.contributor.authorHogerzeil, HV
dc.contributor.authorRägo, S
dc.contributor.authorKopp, S
dc.contributor.authorMendy, C
dc.contributor.authorBalocco, R
dc.contributor.authorGould, A
dc.contributor.authorKuwana, R
dc.contributor.authorMehmandoust, M
dc.contributor.authorMubangizi, D
dc.contributor.authorSaboartova, J
dc.contributor.authorStreipa, I
dc.contributor.authorWorku, WZ
dc.contributor.authorYin, H
dc.contributor.authorvan Zyl, A
dc.contributor.authorAzatyan, S
dc.contributor.authorHetzke, J
dc.contributor.authorMaruyama, Y
dc.contributor.authorOndari, C
dc.contributor.authorThéry, RF
dc.contributor.authorWood, DJ
dc.date.accessioned2013-06-12T06:28:18Z
dc.date.available2013-06-12T06:28:18Z
dc.date.issued2010
dc.identifier.citationWorld Health Organ Tech Rep Ser. 2010;(957):1-276, back coveren
dc.identifier.urihttp://hinari-gw.who.int/whalecomwww.ncbi.nlm.nih.gov/whalecom0/pubmed/20560300
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/31882
dc.description.abstractThe Expert Committee on Specifications for Pharmaceutical Preparations works towards clear, independent and practical standards and guidelines for the quality assurance of medicines. Standards are developed by the Committee through worldwide consultation and an international consensus-building process. The following new guidelines were adopted and recommended for use: good practices for pharmaceutical quality control laboratories; supplementary guidelines for active pharmaceutical ingredients; good manufacturing practices for pharmaceutical products containing hazardous substances; good manufacturing practices for sterile pharmaceutical products; good distribution practices for pharmaceutical products; guidelines on the requalification of prequalified dossiers: and guidelines for the preparation of a contract research organization master file.en
dc.language.isoenen
dc.publisherUniversity of Nairobien
dc.titleWHO Expert Committee on specifications for pharmaceutical preparations.en
dc.typeArticleen
local.publisherSchool of medicine,University of Nairobien


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