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의료기기 품목 재분류 및 차등 관리방안 연구

A Study on Classification and Differential Grade Management for Medical Devices

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초록

With drastic change in the market and technology of medical devices, a comparative analysis is necessary in advanced systems internationally in order to prepare domestically applicable plans for improvement in classification and differential grade management for items of medical devices. This research examines and analyzes the differences of definition and legal systems of medical devices among Korea, United States, EU, Japan and China, and investigates classification and grading system of each country to identify disadvantages of classification and grading structures for medical device in Korea. This research suggests ways to supplement the disadvantages of domestic classification and grading system of medical devices, and elicits differential management plans for medical devices.

Abstract

With drastic change in the market and technology of medical devices, a comparative analysis is necessary in advanced systems internationally in order to prepare domestically applicable plans for improvement in classification and differential grade management for items of medical devices. This research examines and analyzes the differences of definition and legal systems of medical devices among Korea, United States, EU, Japan and China, and investigates classification and grading system of each country to identify disadvantages of classification and grading structures for medical device in Korea. This research suggests ways to supplement the disadvantages of domestic classification and grading system of medical devices, and elicits differential management plans for medical devices.

참고문헌 (27)

  1. The Comparative Legal Research on the Safety System of Food and Drug Administration, "C.H. Park", Ministry of Food and Drug Safety, 40~42 (2009)
  2. A study on the new medical devices(medical supplies)assortment system, "K.M. Lee", Ministry of Food and Drug Safety, 1~342 (2009)
  3. A study on the new medical devices(Medical instruments) assortment system, "K.M. Lee", Ministry of Food and Drug Safety, 1~61 (2010)
  4. The study on the establishment of the classification system of medical devices(dental materials), "K.M. Kim", Ministry of Food and Drug Safety, 1~40 (2011)
  5. A study to re-define and re-classify medical devices under the category of Devices for Physical Treatments, "Y. Kim", Ministry of Food and Drug Safety, 1~306 (2015)
  6. 김용우, "의료기기 일괄허가 및 기술문서 심사를 위한 품목별 길라잡이 개발", 의공학회지, 31(4), pp.280~284 (2010), 대한의용생체공학회
  7. 박기정, "의료기기 허가․기술문서 원자재 작성 가이드라인 개발", 의공학회지, 31(6), pp.434~437 (2010), 대한의용생체공학회
  8. "Medical Device Act", ~
  9. "Enforcement Decree of the Medical Device Act", ~
  10. "Enforcement Regulations of the Medical Device Act", ~
  11. "Ministry of Food and Drug Safety Notification No. 2016-79", ~
  12. "21 USC, Section 321-399", ~
  13. "21 CFR, Part 800-1299", ~
  14. "Medical Device Directive 93", 42, ~
  15. "Active Implantable Medical Devices 90", 385, ~
  16. "In Vitro Diagnostic Medical Device Directive 98", 79, ~
  17. "Directive 2007", 47, ~
  18. "Act on Securing Quality, Efficacy and Safety of Products Including Pharmaceuticals and Medical Devices", ~
  19. "Order for Enforcement of the Act on Securing Quality, Efficacy and Safety of Products Including Pharmaceuticals and Medical Devices", ~
  20. "Regulation for Enforcement of the Act on Securing Quality, Efficacy and Safety of Products Including Pharmaceuticals and Medical Devices", ~
  21. "Pharmaceutical and Food Safety Bureau Notice No. 0720022", ~
  22. "Decree of the State Council of the People's Republic of China. No. 650", ~

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