The implementation of the African union model law on medical products regulation and the establishment of the African medicines agency

dc.contributor.advisorWard, Kim
dc.contributor.authorNcube, Bakani Mark
dc.date.accessioned2023-02-27T07:34:06Z
dc.date.accessioned2024-10-29T13:17:57Z
dc.date.available2023-02-27T07:34:06Z
dc.date.available2024-10-29T13:17:57Z
dc.date.issued2022
dc.description>Magister Scientiae - MScen_US
dc.description.abstractWithin 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 in national medicines regulatory authorities (NMRAs) and ineffective regional collaborations among NMRAs. In response to national regulatory challenges, a number of regional harmonisation efforts were introduced through the African Medicines Regulatory Harmonisation (AMRH) initiative to, among others, expedite market authorisation of medical products and to facilitate the alignment of national legislative frameworks with the African Union (AU) Model Law on Medical Products Regulation.en_US
dc.identifier.urihttps://hdl.handle.net/10566/16339
dc.language.isoenen_US
dc.publisherUniversity of the Western Capeen_US
dc.rights.holderUniversity of the Western Capeen_US
dc.subjectPharmaceutical policyen_US
dc.subjectAfrican Medicines Regulatory Harmonisation Initiativeen_US
dc.subjectLegislationen_US
dc.subjectAfricaen_US
dc.subjectMedicineen_US
dc.titleThe implementation of the African union model law on medical products regulation and the establishment of the African medicines agencyen_US

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