Ensuring patient safety: Best practices in medical device software development based on IEC 62304

Descripción del Articulo

Medical device software plays a crucial role in modern healthcare, responsible for a wide range of functions, from monitoring vital signs to administering treatments. However, software failures can have serious consequences, including patient death. In response to this situation, the IEC 62304 stand...

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Detalles Bibliográficos
Autores: Casma Angulo, Pablo Ivan, Meza Balvin, Sandra Jeannet
Formato: tesis de maestría
Fecha de Publicación:2025
Institución:Universidad de San Martín de Porres
Repositorio:USMP-Institucional
Lenguaje:inglés
OAI Identifier:oai:repositorio.usmp.edu.pe:20.500.12727/19426
Enlace del recurso:https://hdl.handle.net/20.500.12727/19426
Nivel de acceso:acceso embargado
Materia:Medical equipment
Registration
FDA
Software
Development methodology
https://purl.org/pe-repo/ocde/ford#1.02.01
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dc.title.es_PE.fl_str_mv Ensuring patient safety: Best practices in medical device software development based on IEC 62304
title Ensuring patient safety: Best practices in medical device software development based on IEC 62304
spellingShingle Ensuring patient safety: Best practices in medical device software development based on IEC 62304
Casma Angulo, Pablo Ivan
Medical equipment
Registration
FDA
Software
Development methodology
https://purl.org/pe-repo/ocde/ford#1.02.01
title_short Ensuring patient safety: Best practices in medical device software development based on IEC 62304
title_full Ensuring patient safety: Best practices in medical device software development based on IEC 62304
title_fullStr Ensuring patient safety: Best practices in medical device software development based on IEC 62304
title_full_unstemmed Ensuring patient safety: Best practices in medical device software development based on IEC 62304
title_sort Ensuring patient safety: Best practices in medical device software development based on IEC 62304
author Casma Angulo, Pablo Ivan
author_facet Casma Angulo, Pablo Ivan
Meza Balvin, Sandra Jeannet
author_role author
author2 Meza Balvin, Sandra Jeannet
author2_role author
dc.contributor.advisor.fl_str_mv Cuadros Ricra, Ruben Dario
dc.contributor.author.fl_str_mv Casma Angulo, Pablo Ivan
Meza Balvin, Sandra Jeannet
dc.subject.es_PE.fl_str_mv Medical equipment
Registration
FDA
Software
Development methodology
topic Medical equipment
Registration
FDA
Software
Development methodology
https://purl.org/pe-repo/ocde/ford#1.02.01
dc.subject.ocde.es_PE.fl_str_mv https://purl.org/pe-repo/ocde/ford#1.02.01
description Medical device software plays a crucial role in modern healthcare, responsible for a wide range of functions, from monitoring vital signs to administering treatments. However, software failures can have serious consequences, including patient death. In response to this situation, the IEC 62304 standard establishes a set of processes and requirements designed to ensure the safety and effectiveness of software used in medical devices, mitigating the risks associated with their use. In this article we explore the importance of developing medical software under the guidelines of IEC 62304, focusing on patient protection, risk identification and management and the implementation of good practices throughout the software life cycle, the objective of the article is to provide good practices for the development of software for medical equipment, based on the IEC 62304 standard, in order to ensure safety and reliability, we complement with the presentation of an implementation plan that focuses on the objectives of the process, the activities to be carried out and the required documentation, which is key to a certification and registration process with the FDA, As a result we present an assessment from the risk in the adoption of the standard, as well as statistics of the main failures presented in devices that have not followed the recommendations of the standard and as a conclusion we present the advantages and disadvantages in compliance with the standard.
publishDate 2025
dc.date.accessioned.none.fl_str_mv 2025-11-05T14:25:27Z
dc.date.available.none.fl_str_mv 2025-11-05T14:25:27Z
dc.date.embargoEnd.none.fl_str_mv 2027-11-05
dc.date.issued.fl_str_mv 2025
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spelling Cuadros Ricra, Ruben DarioCasma Angulo, Pablo IvanMeza Balvin, Sandra Jeannet2025-11-05T14:25:27Z2025-11-05T14:25:27Z20252027-11-05https://hdl.handle.net/20.500.12727/19426Medical device software plays a crucial role in modern healthcare, responsible for a wide range of functions, from monitoring vital signs to administering treatments. However, software failures can have serious consequences, including patient death. In response to this situation, the IEC 62304 standard establishes a set of processes and requirements designed to ensure the safety and effectiveness of software used in medical devices, mitigating the risks associated with their use. 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