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Substandard and falsified medical product recalls in Zambia from 2018 to 2021 and implications on the quality surveillance systems

BACKGROUND: Substandard and falsified (SF) medical products are removed from circulation through a process called ‘product recall’ by medicines regulatory agencies. In Zambia, the Zambia Medicines Regulatory Authority (ZAMRA) is responsible for recalling SF medical products from the Zambian market t...

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Detalles Bibliográficos
Autores principales:	Chabalenge, Billy, Jere, Elimas, Nanyangwe, Namuchindo, Hikaambo, Christabel, Mudenda, Steward, Banda, Michelo, Kalungia, Aubrey, Matafwali, Scott
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	SAGE Publications 2022
Materias:	Medicine Quality and Pharmaceutical Manufacturing - What Does Good Look Like?
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9806395/ https://www.ncbi.nlm.nih.gov/pubmed/36601496 http://dx.doi.org/10.1177/27550834221141767

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