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Medical Device Development Process, and Associated Risks and Legislative Aspects-Systematic Review
P. Marešová, B. Klímová, J. Honegr, K. Kuča, WNH. Ibrahim, A. Selamat,
Jazyk angličtina Země Švýcarsko
Typ dokumentu systematický přehled
NLK
Directory of Open Access Journals
od 2013
Free Medical Journals
od 2013
PubMed Central
od 2013
Europe PubMed Central
od 2013
Open Access Digital Library
od 2013-01-01
Open Access Digital Library
od 2013-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2013
PubMed
32903646
DOI
10.3389/fpubh.2020.00308
Knihovny.cz E-zdroje
- Publikační typ
- systematický přehled MeSH
Objective: Medical device development, from the product's conception to release to market, is very complex and relies significantly on the application of exact processes. This paper aims to provide an analysis and summary of current research in the field of medical device development methodologies, discuss its phases, and evaluate the associated legislative and risk aspects. Methods: The literature search was conducted to detect peer-reviewed studies in Scopus, Web of Science, and Science Direct, on content published between 2007 and November 2019. Based on exclusion and inclusion criteria, 13 papers were included in the first session and 11 were included in the second session. Thus, a total of 24 papers were analyzed. Most of the publications originated in the United States (7 out of 24). Results: The medical device development process comprises one to seven stages. Six studies also contain a model of the medical device development process for all stages or for just some of the stages. These studies specifically describe the concept stage during which all uncertainties, such as the clinical need definition, customer requirements/needs, finances, reimbursement strategy, team selection, and legal aspects, must be considered. Conclusion: The crucial factor in healthcare safety is the stability of factors over a long production time. Good manufacturing practices cannot be tested on individual batches of products; they must be inherently built into the manufacturing process. The key issues that must be addressed in the future are the consistency in the classification of devices throughout the EU and globally, and the transparency of approval processes.
Biomedical Research Centrum University Hospital Hradec Kralove Hradec Kralove Czechia
Faculty of Informatics and Management University of Hradec Kralove Hradec Kralove Czechia
Citace poskytuje Crossref.org
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