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Materiovigilance Programme of India: A scheme to assure cardiovascular devices safety surveillance

The Materiovigilance Programme of India (MvPI) has been implemented to ensure the safety of medical devices including cardiovascular devices (MD-CVD). This article describes the role of MvPI surveillance system that comprehensively collects, collates and analyses the adverse events associated with M...

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Detalles Bibliográficos
Autores principales: Kalaiselvan, V., Tripathi, Santanu Kumar, Prakash, Jai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7474122/
https://www.ncbi.nlm.nih.gov/pubmed/32861393
http://dx.doi.org/10.1016/j.ihj.2020.06.009
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author Kalaiselvan, V.
Tripathi, Santanu Kumar
Prakash, Jai
author_facet Kalaiselvan, V.
Tripathi, Santanu Kumar
Prakash, Jai
author_sort Kalaiselvan, V.
collection PubMed
description The Materiovigilance Programme of India (MvPI) has been implemented to ensure the safety of medical devices including cardiovascular devices (MD-CVD). This article describes the role of MvPI surveillance system that comprehensively collects, collates and analyses the adverse events associated with MD-CVD and also its supplementing role to the Central Drugs Standard Control Organization for taking regulatory decision to reduce the health burden on account of adverse events due to medical devices to the patients based on the evidence based data. This article is expected to stimulate ethical reporting of adverse events due to MD-CVD at MvPI.
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spelling pubmed-74741222020-09-15 Materiovigilance Programme of India: A scheme to assure cardiovascular devices safety surveillance Kalaiselvan, V. Tripathi, Santanu Kumar Prakash, Jai Indian Heart J Opinion Paper The Materiovigilance Programme of India (MvPI) has been implemented to ensure the safety of medical devices including cardiovascular devices (MD-CVD). This article describes the role of MvPI surveillance system that comprehensively collects, collates and analyses the adverse events associated with MD-CVD and also its supplementing role to the Central Drugs Standard Control Organization for taking regulatory decision to reduce the health burden on account of adverse events due to medical devices to the patients based on the evidence based data. This article is expected to stimulate ethical reporting of adverse events due to MD-CVD at MvPI. Elsevier 2020 2020-07-01 /pmc/articles/PMC7474122/ /pubmed/32861393 http://dx.doi.org/10.1016/j.ihj.2020.06.009 Text en © 2020 Cardiological Society of India. Published by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Opinion Paper
Kalaiselvan, V.
Tripathi, Santanu Kumar
Prakash, Jai
Materiovigilance Programme of India: A scheme to assure cardiovascular devices safety surveillance
title Materiovigilance Programme of India: A scheme to assure cardiovascular devices safety surveillance
title_full Materiovigilance Programme of India: A scheme to assure cardiovascular devices safety surveillance
title_fullStr Materiovigilance Programme of India: A scheme to assure cardiovascular devices safety surveillance
title_full_unstemmed Materiovigilance Programme of India: A scheme to assure cardiovascular devices safety surveillance
title_short Materiovigilance Programme of India: A scheme to assure cardiovascular devices safety surveillance
title_sort materiovigilance programme of india: a scheme to assure cardiovascular devices safety surveillance
topic Opinion Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7474122/
https://www.ncbi.nlm.nih.gov/pubmed/32861393
http://dx.doi.org/10.1016/j.ihj.2020.06.009
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