The Application of an Integrated Product Development Process to the Design of Medical Equipment

Canciglieri, Osíris; Okumura, Maria Lucia Miyake; Young, Robert I. M.

doi:10.1007/978-3-319-13776-6_25

Cited by 3 publications

(1 citation statement)

References 26 publications

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“…A função do moderador do DFAT é buscar dados detalhados que são as características mais profundas para interpretá-las e direcioná-las como requisitos do produto pelas fases do PDIP, conforme ilustrado e destacado o Projeto Informacional na Figura 1. identificar o profissional especialista na área multidisciplinar e identificar as atividades do usuário para definir os requisitos a ser projetado. A interdisciplinaridade no PDIP orientado para TA envolve-se os usuários indiretos e o usuário final, que é argumentado quando se trata de PDIP de dispositivos ou equipamentos que são utilizados por profissionais prestadores de serviço e os seus usuários (CANCIGLIERI JUNIOR et al, 2015).…”

Section: Design For Assistive Technology No Pdipunclassified

Construção Da Docencia Desafios E Oportunidades: Relato De Experiência Em Uma Escola Pública De São Luís - Maranhão

Batalha¹,

Oliveira²,

Assis³

2019

Educação: Políticas, Estrutura E Organização 5

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Abordagem interdisciplinar do conhecimento. 2. Currículo escolar -Brasil. 3. Educação -Pesquisa -Brasil. 4. Políticas educacionais. I. Ferreira, Gabriella Rossetti. II. Série. CDD 370.1 Elaborado por Maurício Amormino Júnior -CRB6/2422 O conteúdo dos artigos e seus dados em sua forma, correção e confiabilidade são de responsabilidade exclusiva dos autores. 2019 Permitido o download da obra e o compartilhamento desde que sejam atribuídos créditos aos autores, mas sem a possibilidade de alterá-la de nenhuma forma ou utilizá-la para fins comerciais.

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Section: Design For Assistive Technology No Pdipunclassified

Construção Da Docencia Desafios E Oportunidades: Relato De Experiência Em Uma Escola Pública De São Luís - Maranhão

Batalha¹,

Oliveira²,

Assis³

2019

Educação: Políticas, Estrutura E Organização 5

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Usage-driven problem design for radical innovation in healthcare

2017

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While the diffusion and evaluation of healthcare innovations receive a lot of attention, the early design stages are less studied and potential innovators lack methods to identify where new innovations are necessary and to propose concepts relevant to users. To change this, we propose a structured methodology, Radical Innovation Design (RID), which supports designers who want to work on the unstated needs of potential end users in order to create superior value. In this article, the first part of RID is introduced with its two subprocesses: Problem Design and Knowledge Design. In this first period, RID guides innovators to systematically explore users' problems and evaluate which ones are most pressing in terms of innovation, taking into account existing solutions. The result is an ambition perimeter, composed of a set of value buckets, that is, important usage situations where major problems are experienced and the current solutions provide little or no relief. The methodology then moves on to Solution Design and Business Design (which are not detailed in this article) to address the value buckets identified. With its emphasis on problem exploration, RID differs from methods based on early prototyping. The RID methodology has been validated in various industrial sectors and is well-adapted for healthcare innovation. To exemplify the methodology, we present a case study in dental imagery performed by 10 students in 8 weeks. This example demonstrates how RID favours efficiency in Problem Design and allows designers to explore unaddressed and sometimes undeclared user needs.

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Development of 18 Quality Control Gates for Additive Manufacturing of Error Free Patient-Specific Implants

et al. 2019

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Unlike subtractive manufacturing technologies, additive manufacturing (AM) can fabricate complex shapes from the macro to the micro scale, thereby allowing the design of patient-specific implants following a biomimetic approach for the reconstruction of complex bone configurations. Nevertheless, factors such as high design variability and changeable customer needs are re-shaping current medical standards and quality control strategies in this sector. Such factors necessitate the urgent formulation of comprehensive AM quality control procedures. To address this need, this study explored and reported on a variety of aspects related to the production and the quality control of additively manufactured patient-specific implants in three different AM companies. The research goal was to develop an integrated quality control procedure based on the synthesis and the adaptation of the best quality control practices with the three examined companies and/or reported in literature. The study resulted in the development of an integrated quality control procedure consisting of 18 distinct gates based on the best identified industry practices and reported literature such as the Food and Drug Administration (FDA) guideline for AM medical devices and American Society for Testing and Materials (ASTM) standards, to name a few. This integrated quality control procedure for patient-specific implants seeks to prepare the AM industry for the inevitable future tightening in related medical regulations. Moreover, this study revealed some critical success factors for companies developing additively manufactured patient-specific implants, including ongoing research and development (R&D) investment, investment in advanced technologies for controlling quality, and fostering a quality improvement organizational culture.

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The Application of an Integrated Product Development Process to the Design of Medical Equipment

Cited by 3 publications

References 26 publications

Construção Da Docencia Desafios E Oportunidades: Relato De Experiência Em Uma Escola Pública De São Luís - Maranhão

Construção Da Docencia Desafios E Oportunidades: Relato De Experiência Em Uma Escola Pública De São Luís - Maranhão

Usage-driven problem design for radical innovation in healthcare

Development of 18 Quality Control Gates for Additive Manufacturing of Error Free Patient-Specific Implants

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