Medical device design within the ISO 13485 framework

dc.check.entireThesisEntire Thesis Restricted
dc.check.opt-outYesen
dc.check.reasonReleasing this thesis would cause substantial prejudice to the commercial interests of University College Corken
dc.contributor.advisorCantillon-Murphy, Padraigen
dc.contributor.authorO'Shea, Conor
dc.contributor.funderIrish Research Council for Science, Engineering and Technologyen
dc.date.accessioned2017-02-14T13:30:31Z
dc.date.issued2017
dc.date.submitted2017
dc.description.abstractThe design and development of medical devices has become an increasing complex and regulated process. Little if any consideration is given to the regulatory requirements when developing medical devices in universities. This has resulted in an imposing barrier preventing academic innovation reaching clinical adoption. The scope of universities is not to become the legal manufacturer of medical devices. However, should the development of novel devices ever aim to benefit patient care and reach a clinical setting, design controls must be implemented throughout the project life cycle to demonstrate feasibility and safety. The aim of this thesis is to develop user-centred technologies which comply with industrial design control practices whilst helping to bolster and promote innovation within academia. Four projects relating to medical devices have been designed in response to well-defined and end-user-originated clinical needs. These devices can serve as the exemplar for the framework developed in this work with each reaching staggered phases of development within a controlled design process. Although unique, the devices have significant overlapping characteristics that lend the devices to parallel development, leveraging in-house know-how and ‘lessons learned’ into the process of innovation. This thesis focuses on the novelty and design of the aforementioned projects in a discrete structured approach and reflects on the development of each project within the context of a design control process which was developed as part of this work. It is the ultimate goal of this work to develop a flexible structured system compliant with the international requirements for product design and development which may be exported internationally. However, the full execution of this ambition was limited due physical, and financial limitations. This manuscript will describe the technical and commercial opportunity of devices and reflects on the success of developing same within a design control process developed as part of this work.en
dc.description.sponsorshipIrish Research Council for Science, Engineering and Technology (Grant GOIPG/2013/137)en
dc.description.statusNot peer revieweden
dc.description.versionAccepted Version
dc.format.mimetypeapplication/pdfen
dc.identifier.citationO'Shea, C. 2017. Medical device design within the ISO 13485 framework. PhD Thesis, University College Cork.en
dc.identifier.endpage227en
dc.identifier.urihttps://hdl.handle.net/10468/3630
dc.language.isoenen
dc.publisherUniversity College Corken
dc.rights© 2017, Conor O'Shea.en
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/en
dc.subjectMedical devicesen
dc.subjectMedical device designen
dc.subjectISO 13485 frameworken
dc.thesis.opt-outtrue
dc.titleMedical device design within the ISO 13485 frameworken
dc.typeDoctoral thesisen
dc.type.qualificationlevelDoctoral Degree (Structured)en
dc.type.qualificationnamePHD (Engineering)en
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