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植入性医疗器械的电子监管 被引量:1

Electronic Regulation Mode on Implantable Medical Device
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摘要 目的:探讨我国植入性医疗器械监管改革的有效方法。方法:采取文献检索、比较研究、状况研究、发展性研究和个案分析的方法进行分析。结果:植入性医疗器械领域发生问题的根本原因是相关信息的严重不真实、不对称。结论:建立植入性医疗器械电子监管系统,即建立各种既独立又相互联系实时更新的动态数据库,保证信息公开、透明,杜绝虚假信息的传递,维护植入性医疗器械行业的良好秩序,保障广大公众的切身利益。 OBJECTIVE: To discuss the methods of implantable medical device supervision reform. METHODS: Methods of literature review, comparative study, the research of situation, developmental study and case study were adopted. RESULTS:It is the untrue and asymmetric information of Jmplantable medical device that results in Jmproper behavior in the implantable medical device industry. CONCLUSIONS: A implantable medical device electronic monitoring system, namely establishing the independent but interrelated real-time dynamic updating of the databases, which would guarantee the information of implantable medical device is open and transparent, eliminate false food information transmission, vindicate the good order of domestic implantable medical device industry and protect the vital interests of the public.
出处 《中国医疗器械杂志》 CAS 2009年第2期124-127,共4页 Chinese Journal of Medical Instrumentation
基金 国家自然科学基金(NO.30801127) 辽宁省社科规划基金题(NO.L07DJY069) 辽宁省社科联课题(NO.2006lnsklktjjx-254-73) 大连市社科联课题(NO.06DLSK144).
关键词 植入性医疗器械 电子监管 互联网 不正当行为 implantable medical device, electronic regulation, internet, improper behavior
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参考文献35

  • 1Curfman GD, Morrissey S, Drazen JM. A pivotal medical-device case[J]. N Engl J Med.,2008,358(1):76-7.
  • 2Maisel WH. Semper fidelis--consumer protection for patients with implanted medical devices[J]. N E ngl J Med.,2008, 358(10):985-7.
  • 3Myerburg RJ, Feigal DW Jr, Lindsay BD. Life-threatening malfunction of implantable cardiac devices[J]. N Engl J Med.2006, 354 (22): 2309-11.
  • 4Maisel WH. Safety issues involving medical devices: implications of recent implantable cardioverter-defibrillator malfunctions[J]. JAMA., 2005, 294(8):955-8.
  • 5Maisel WH. Medical device regulation: an introduction for the practicing physician[J]. Ann Intern Med,2004,140(4):296-302.
  • 6Maisel WH, Sweeney MO, Stevenson WG, et, al.Recalls and safety alerts involving pacemakers and implantable cardioverter-defibrillator generators[J]. JAMA. 2001, 286(7):793-9.
  • 7Brown SL, Bright RA, Tavris DR. Medical device epidemiology and surveillance: patient safety is the bottom line[J]. Expert Rev Med Devices. 2004,1(1): 1-2.
  • 8Marinac-Dabic D, Bonhomme M, Loyo-Berrios N, Gross T, Ciperson R, Gardner S, Marcarelli M. Medical devices post-approval studies program: vision, strategies, challenges and opportunities[J]. Food Drug Law J. 2007, 62(3):597-604.
  • 9Felten RP, Ogden NR, Pe?a C, Provost MC, Schlosser M J, Witten CM. The Food and Drug Administration medical device review process: clearance of a clot retriever for use in ischemic stroke[J]. Stroke, 2005,36(2):404-6.
  • 10李基业.应用生物材料补片修补腹壁切口疝应注意的一些问题[J].中华外科杂志,2007,45(21):1446-1448. 被引量:15

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