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

Internet

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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