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Medical device regulation and oversight in African countries: a scoping review of literature and development of a conceptual framework
Regulatory and other governance arrangements influence the introduction of medical devices into health systems and are essential for ensuring their effective and safe use. Challenges with medical device safety, quality and use are documented globally, with evidence suggesting these are linked to poo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10414093/ https://www.ncbi.nlm.nih.gov/pubmed/37558270 http://dx.doi.org/10.1136/bmjgh-2023-012308 |
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author | Nasir, Naima Molyneux, Sassy Were, Fred Aderoba, Adeniyi Fuller, Sebastian S |
author_facet | Nasir, Naima Molyneux, Sassy Were, Fred Aderoba, Adeniyi Fuller, Sebastian S |
author_sort | Nasir, Naima |
collection | PubMed |
description | Regulatory and other governance arrangements influence the introduction of medical devices into health systems and are essential for ensuring their effective and safe use. Challenges with medical device safety, quality and use are documented globally, with evidence suggesting these are linked to poor governance. Yet, medical device regulation and oversight remain inadequately defined and described, particularly in low-income and middle-income settings. Through this review, we sought to examine the literature available on regulatory and oversight processes for medical devices in African countries. Following a systematic approach, we searched academic databases including PubMed, Embase (Ovid) and MEDLINE (Ovid), supplemented by search for grey literature and relevant organisational websites, for documents describing medical device regulation and oversight in African countries. We summarised the data to present key actors, areas for regulation and oversight and challenges. A total of 39 documents reporting regulation and oversight of medical devices were included for analysis. Regulatory and oversight guidelines and processes were reported as inadequate, including limited pre-market testing, reliance on international certifications and limited processes for post-market monitoring and reporting of adverse events. Challenges for regulation and oversight reported included inadequate funding, personnel and technical expertise to perform regulatory functions. The literature highlighted gaps in guidelines for donated medical devices and in information on governance processes at the national level. The current literature provides a general overview of medical device regulatory guidelines and limited evidence on the implementation of regulatory/oversight processes at national and especially subnational levels. We recommend further research to elucidate existing governance arrangements for medical devices within African countries and propose a conceptual framework to inform future studies. The framework provides entry points for careful examination of governance and oversight in policy and practice, the exploration of governance realities across the health system and the influence of wider system dynamics. |
format | Online Article Text |
id | pubmed-10414093 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-104140932023-08-11 Medical device regulation and oversight in African countries: a scoping review of literature and development of a conceptual framework Nasir, Naima Molyneux, Sassy Were, Fred Aderoba, Adeniyi Fuller, Sebastian S BMJ Glob Health Original Research Regulatory and other governance arrangements influence the introduction of medical devices into health systems and are essential for ensuring their effective and safe use. Challenges with medical device safety, quality and use are documented globally, with evidence suggesting these are linked to poor governance. Yet, medical device regulation and oversight remain inadequately defined and described, particularly in low-income and middle-income settings. Through this review, we sought to examine the literature available on regulatory and oversight processes for medical devices in African countries. Following a systematic approach, we searched academic databases including PubMed, Embase (Ovid) and MEDLINE (Ovid), supplemented by search for grey literature and relevant organisational websites, for documents describing medical device regulation and oversight in African countries. We summarised the data to present key actors, areas for regulation and oversight and challenges. A total of 39 documents reporting regulation and oversight of medical devices were included for analysis. Regulatory and oversight guidelines and processes were reported as inadequate, including limited pre-market testing, reliance on international certifications and limited processes for post-market monitoring and reporting of adverse events. Challenges for regulation and oversight reported included inadequate funding, personnel and technical expertise to perform regulatory functions. The literature highlighted gaps in guidelines for donated medical devices and in information on governance processes at the national level. The current literature provides a general overview of medical device regulatory guidelines and limited evidence on the implementation of regulatory/oversight processes at national and especially subnational levels. We recommend further research to elucidate existing governance arrangements for medical devices within African countries and propose a conceptual framework to inform future studies. The framework provides entry points for careful examination of governance and oversight in policy and practice, the exploration of governance realities across the health system and the influence of wider system dynamics. BMJ Publishing Group 2023-08-09 /pmc/articles/PMC10414093/ /pubmed/37558270 http://dx.doi.org/10.1136/bmjgh-2023-012308 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Research Nasir, Naima Molyneux, Sassy Were, Fred Aderoba, Adeniyi Fuller, Sebastian S Medical device regulation and oversight in African countries: a scoping review of literature and development of a conceptual framework |
title | Medical device regulation and oversight in African countries: a scoping review of literature and development of a conceptual framework |
title_full | Medical device regulation and oversight in African countries: a scoping review of literature and development of a conceptual framework |
title_fullStr | Medical device regulation and oversight in African countries: a scoping review of literature and development of a conceptual framework |
title_full_unstemmed | Medical device regulation and oversight in African countries: a scoping review of literature and development of a conceptual framework |
title_short | Medical device regulation and oversight in African countries: a scoping review of literature and development of a conceptual framework |
title_sort | medical device regulation and oversight in african countries: a scoping review of literature and development of a conceptual framework |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10414093/ https://www.ncbi.nlm.nih.gov/pubmed/37558270 http://dx.doi.org/10.1136/bmjgh-2023-012308 |
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