Browsing Faculty of Natural Science by Author "Ward, Kim"
Now showing items 1-5 of 5
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The implementation of the African union model law on medical products regulation and the establishment of the African medicines agency
Ncube, Bakani Mark (University of the Western Cape, 2022)Within Africa, there is insufficient access to quality, safe, efficacious and affordable medical products which can partly be attributed to lack of robust regulatory systems, a lack of competent regulatory professionals ... -
Perceptions of the pharmaceutical industry and regulators in South Africa towards registration harmonisation in the Southern African Development Community (SADC)
Dhanraj, Keshnee (University of the Western Cape, 2021)Medicines have to be regulated in an effort to monitor their quality, safety, and efficacy. The process of medicines registration is lengthy, costly, and document-heavy. Many countries have limited expertise and resources ... -
Post-market assessment of the quality of first line regimen fixed-dose combination antiretrovirals in South Africa
Suleiman, Reem Abdallah S. (University of the Western Cape, 2017)The rapid increase in access to new antiretrovirals (ARVs) worldwide and, especially in sub-Saharan Africa, coupled with the well-documented problem of poor quality ARVs in developing countries has underscored the need for ... -
Review of the effectiveness of the medicines regulatory systems in Zambia over the period 1995 to 2015
Kabali, Emmanuel (University of the Western Cape, 2018)Due to inadequacy of data on the effectiveness of medicines regulatory systems in Zambia, this study was framed. The aim was to evaluate legislative provisions for medicines regulation under three legalregulatory- frameworks ... -
Review of the effectiveness of the medicines regulatory systems in Zambia over the period 1995 to 2015
Kabali, Emmanuel (University of the Western Cape, 2018)Due to inadequacy of data on the effectiveness of medicines regulatory systems in Zambia, this study was framed. The aim was to evaluate legislative provisions for medicines regulation under three legalregulatory- frameworks ...