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dc.contributor.authorThoithi, G.N.
dc.contributor.authorAbuga, K.O
dc.contributor.authorNguyo, J.M
dc.contributor.authorMukindia, G
dc.contributor.authorKingondu, O
dc.contributor.authorNgugi, J.K.
dc.contributor.authorKibwage, IO
dc.date.accessioned2013-02-22T07:57:33Z
dc.date.issued2002
dc.identifier.citationEast and Central African Journal of Pharmaceutical Sciences Vol.5(2) 2002: 28-32en
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/10705
dc.description.abstractThe Drug Analysis and Research Unit received and analyzed 261 drug samples over a five-year period, 1996 to 2000. Samples were received from regulatory authorities, local industry, non-governmental organizations, hospitals and private practitioners. The samples analyzed constituted 59.8 % locally manufactured and 40.2 % imported products. The overall rate of failure to comply with quality specifications set out in the respective monographs was 21.1 %. This represents 24.6 % and 16.2 % of the locally manufactured and imported drugs, respectively.en
dc.language.isoenen
dc.subjectQuality controlen
dc.subjectActive pharmaceutical ingredient content,en
dc.subjectDissolution.en
dc.titleDrug quality control in Kenya:Observation in drug analysis and research unit during the period 1996-2000en
dc.typeArticleen
local.embargo.terms6 monthsen
local.publisherDrug analysis and research unit Department o pharmaceutical chemistry faculty of pharmacy ,University of Nairobien


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