Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/16365
Full metadata record
DC FieldValueLanguage
dc.contributor.authorIvanović, Lozica-
dc.contributor.authorRackov, Milan-
dc.contributor.authorStojanovic, Blaza-
dc.contributor.authorPenčić, Marko-
dc.contributor.authorČavić, Maja-
dc.contributor.authorMiladinovic, Slavica-
dc.date.accessioned2023-02-09T11:06:41Z-
dc.date.available2023-02-09T11:06:41Z-
dc.date.issued2022-
dc.identifier.citationIvanović, L., Rackov, M., Stojanović, B., Penčić, M., Čavić, M., Miladinović, S. (2022). Design and Development of Medical Devices. In: Lalic, B., Gracanin, D., Tasic, N., Simeunović, N. (eds) Proceedings on 18th International Conference on Industrial Systems – IS’20. IS 2020. Lecture Notes on Multidisciplinary Industrial Engineering. Springer, Cham. https://doi.org/10.1007/978-3-030-97947-8_6en_US
dc.identifier.isbn978-3-030-97946-1en_US
dc.identifier.issn2522-5022en_US
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/16365-
dc.description.abstractThe medical device industry is one of the fastest growing industries. Medical devices cover a wide range of products for medical use, ranging from the simplest to the most sophisticated medical equipment. Thanks to today’s rapid development in both medicine and technology, the development of medical devices has been intensified. Given the multidisciplinary characteristics of such devices and their environment, the process of developing medical devices involves some special characteristics. Due to their potentially harmful effects in the interaction with tissues and organs, compliance with the various directives is of particular importance. For these reasons, it is necessary to carefully follow all steps in the design and manufacture of medical devices in order to obtain regulatory approval and licensing of the products, so that their implementation is safe for users. This paper demonstrates that medical device design is a unique and complex process which requires an organized development strategy that ensures that the product meets design and user goals, is technically reliable, and can be produced safely and efficiently.en_US
dc.language.isoenen_US
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.sourceIndustrial Innovation in Digital Age : Proceedings on 18th International Conference on Industrial Systems – IS’20-
dc.subjectMedical device Design process Design methodology Product development Directivesen_US
dc.titleDesign and Development of Medical Devicesen_US
dc.typebookParten_US
dc.description.versionAuthor's versionen_US
dc.identifier.doi10.1007/978-3-030-97947-8_6en_US
dc.type.versionPublishedVersionen_US
Appears in Collections:Faculty of Engineering, Kragujevac

Page views(s)

388

Downloads(s)

43

Files in This Item:
File Description SizeFormat 
499370_1_En_6_Chapter_Author.pdf1.3 MBAdobe PDFThumbnail
View/Open


Items in SCIDAR are protected by copyright, with all rights reserved, unless otherwise indicated.