On the universality of medical device regulations: the case of Benin

BACKGROUND: Regulatory frameworks surrounding medical devices (MDs) and medical locations are of utter importance for safeguarding patients and users, and for granting a universal access to healthcare. Currently, as the main existing regulatory frameworks are drafted by high-income countries, they p...

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Detalles Bibliográficos
Autores principales: Maccaro, A., Piaggio, D., Leesurakarn, S., Husen, N., Sekalala, S., Rai, S., Pecchia, L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9375389/
https://www.ncbi.nlm.nih.gov/pubmed/35962389
http://dx.doi.org/10.1186/s12913-022-08396-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9375389/
https://www.ncbi.nlm.nih.gov/pubmed/35962389
http://dx.doi.org/10.1186/s12913-022-08396-2

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