• 제목/요약/키워드: 의료기기 산업

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한국 의료기기산업의 공간적 특성에 관한 연구 (A Study on Spatial Characteristics of the Medical Device Industry in Korea)

  • 황인균
    • 한국경제지리학회지
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    • 제22권1호
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    • pp.1-17
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    • 2019
  • 이 논문의 목적은 지역산업정책 추진에 따른 의료기기 산업의 공간적 특성을 고찰하는데 있다. 이를 위해, 정부지원에 따른 생산 활동의 생산성과 판매 활동에 의한 수익성을 공간별로 살펴볼 수 있는 연구방법론을 제시하였다. 정부의 대규모 지원이 '선별적 지원' 방식에 의해 지역별로 편재됨에 따라 산업의 생산성과 수익성의 공간적 특성이 상이하게 나타났다. 이러한 맥락에서 정부의 지역산업 정책을 세 가지 측면에서 검토한 결과는 다음과 같다. 첫째, 정부지원이 생산성 강화와 수익성 확보로 귀결되지 않았다. 둘째, 지역적 차원에서 높은 생산성이 반드시 높은 수익성으로 직결되지도 않았다. 마지막으로, 수익성 측면에서 높은 시장점유율이 높은 이윤창출을 보장하지도 않았다. 그러므로 정부는 산업 특수성과 정책 지원의 성과를 고려하여 생산성과 수익성 간 연계성이 확보될 수 있도록 지역산업정책의 방향성을 재검토할 필요가 있다.

의료기기 개발 글로벌 인재 양성을 위한 컴퓨터정보기술 융합교육 (Computer and IT Convergence Education for Nurturing Global Human Resources Developing Medical Appliances)

  • 김종완
    • 한국멀티미디어학회:학술대회논문집
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    • 한국멀티미디어학회 2012년도 춘계학술발표대회논문집
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    • pp.219-220
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    • 2012
  • 본 연구에서는 컴퓨터정보공학과 재활공학 그리고 디자인을 융합하여 의료재활기기 산업 인재 양성을 위한 글로벌 정보기술 융합교육 프로그램을 제안한다. 이 목표 달성을 위하여, 세가지 다른 분야의 전공학생들이 학제 융합팀을 구성하고, 방과후 및 방학기간을 이용하여 영어(English), 리더십(Leadership), 혁신(Innovation), 팀워크(Teamwork), 창업 정신(Entrepreneurship)의 ELITE 프로그램을 이수시켜서 글로벌 인재 양성에 기여한다.

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병원내 의료기기 교체의 우선순위 결정을 위한 단순평가법 개발 (Development of Simple Evaluation Method for Determining the Priority of Medical Device Replacement in Hospitals)

  • 서기홍;박은경;최동일
    • 대한의용생체공학회:의공학회지
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    • 제41권6호
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    • pp.256-263
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    • 2020
  • The importance of quality control has been emphasized to maintain safety of patients and satisfaction of medical service with medical devices used in clinic. Accordingly, objective evaluation method and standards consistently has been brought up for demand to replace outdated medical devices in appropriate time and to maintain the quality of medical service. Though many studies made suggestions methods to determine what medical devices to be replaced first, these methods were difficult in practice for its complex evaluation criteria and long time to evaluate. Therefore, in this study, a simple evaluation method is developed to identify and prioritize medical devices that are ought to be replaced. For the development of this simple evaluation method, four major characteristics of technology, safety, finance, and user satisfaction, which are considered in clinics to evaluate medical device replacement, and 14 minor attributes are distinctively selected. Each characteristic is assessed in binary form of "YES" or "NO" to minimize its subjective nature. Using this method to evaluate sampled medical devices belonging to four different characteristics, devices are suggested to be replaced in the current financial year or in the following financial year, or re-evaluated by the end of this financial year. Such results of evaluation can amend the subjective nature of existing evaluation method and give objective standards more promptly.

국내 의료기기 제조업체의 ISO13485:2016 교육 프로그램 개발 및 교육 효과 연구 (A Study on the Development and Effectiveness of ISO13485:2016 Education Programs for Domestic Medical Device Manufacturers)

  • 이슬비;강기호;장원석;권병주
    • 품질경영학회지
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    • 제50권3호
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    • pp.503-515
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    • 2022
  • Purpose: As ISO 13485 was revised in 2016, the domestic GMP (Good Manufacturing Practice) system was also revised and implemented in 2019. However, there are many problems in the domestic medical device industry because most of the small and medium-sized enterprises lack human and material resources. Accordingly, this study was conducted to provide education programs for domestic medical device companies to induce information provision and improve the company's quality management ability. Methods: First, analyze existing education. Second, based on the revised GMP system, a survey paper was produced to investigate difficulties and problems experienced by companies. Third, a two-week survey was conducted on domestic medical device manufacturers, and a total of 77 companies responded to this survey. Fourth, educational program development was conducted based on the results of the survey. Results and Conclusion: The developed education program consists of a total of five sessions. In this study, the educational program developed by grasping the needs of the company through a survey consists of a total of five sessions. The first session consisted of theoretical education and the second to fifth sessions of practical education. Through the education program developed in this study, it is expected to contribute to the overall development of medical device quality by establishing a domestic medical device manufacturing environment that secures the safety and performance of domestic medical device companies.