The domestication of the African Union model law on medical products regulation: Perceived benefits, enabling factors, and challenges

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dc.contributor.authorNcube, Bakani Mark
dc.contributor.authorDube, Admire
dc.contributor.authorWard, Kim
dc.date.accessioned2023-02-28T07:54:58Z
dc.date.available2023-02-28T07:54:58Z
dc.date.issued2023
dc.description.abstractIn 2016, the African Union (AU) Model Law on Medical Products Regulation was endorsed by AU Heads of State and Government. The aims of the legislation include harmonisation of regulatory systems, increasing collaboration across countries, and providing a conducive regulatory environment for medical product/health technology development and scale-up. A target was set to have at least 25 African countries domesticating the model law by 2020. However, this target has not yet been met. This research aimed to apply the Consolidated Framework for Implementation Research (CFIR) in analysing the rationale, perceived benefits, enabling factors, and challenges of AU Model Law domestication and implementation by AU Member States.en_US
dc.identifier.citationNcube, B. M. et al. (2023). The domestication of the African Union model law on medical products regulation: Perceived benefits, enabling factors, and challenges. Frontiers in Medicine, 10, 1117439. https://doi.org/10.3389/fmed.2023.1117439en_US
dc.identifier.issn2296-858X
dc.identifier.urihttps://doi.org/10.3389/fmed.2023.1117439
dc.identifier.urihttp://hdl.handle.net/10566/8468
dc.language.isoenen_US
dc.publisherFrontiers Mediaen_US
dc.subjectPharmaceutical policyen_US
dc.subjectAfrican medicinesen_US
dc.subjectLegislationen_US
dc.subjectMedical healthen_US
dc.subjectAfrican Unionen_US
dc.titleThe domestication of the African Union model law on medical products regulation: Perceived benefits, enabling factors, and challengesen_US
dc.typeArticleen_US

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