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血站数据电文与电子签名管理——相关法规学习与理解 被引量:5

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出处 《中国输血杂志》 CAS CSCD 北大核心 2009年第2期161-164,共4页 Chinese Journal of Blood Transfusion
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参考文献11

  • 1中华人民共和国电子签名法.2005-05-01
  • 2卫生部.血站质量管理规范.2006.4.25.
  • 3中华人民共和国电子签名法释义[OL].http://www.npc.gov.en/npe/flsyywd/jingii/node_2217.htm
  • 4中华人民共和国信息产业部.软件产品管理办法.2009-03-01
  • 5中华人民共和国信息产业部.计算机信息系统集成资质管理办法(试行).1999-11-12
  • 6Food and Drug Administration. CFR 21 Part 11. Electronic Records & Electronic Signatures[OL]. http ://ecfr. gpoaccess. gov/ cgi/t/text/text-idx? c = ecfr&tpl = %2Findex. tpl
  • 7Food and Drug Administration. Guidance for Industry : Part11, Electronic Records; Electronic Signatures- Validation [OL]. http ://www. fda. gov/cder/guidance/index. htm
  • 8Food and Drug Administration. Guidance for Industry: Part 11, Electronic Records; Electronic Signatures-Time Stamps [OL]. http ://www. fda. gov/eder/guidancc/indcx. htm
  • 9Food and Drug Administration. Guidance for Industry: Part 11, Electronic Records; Electronic Signatures-Electronic Copies of Electronic Records [ OL ]. http ://www. fda. gov/cder/gnidance/ index. htm
  • 10Food and Drug Administration. Guidance for Industry: Part 11, Electronic Records; Electronic Signatures-Maintenance of Electronic Records [ OL ]. http://www. fda. gov/cder/guidance/indcx. htm

共引文献42

同被引文献22

  • 1高富平,俞迪飞.电子记录等同于纸面证据的解决方案——兼论《电子签名法》的局限性[J].法学,2004(11):89-98. 被引量:23
  • 2陈保民.血站ISO9000质量管理体系中仪器设备的质量管理[J].中国卫生质量管理,2006,13(5):62-64. 被引量:2
  • 3罗建勇.血站开展全面质量管理的体会[J].中国输血杂志,2006,19(6):509-510. 被引量:8
  • 4U.S. National Archives and Records Administration. Records management guidance for agencies Implementing electronic signature technologies. 2000-10 [ 2009-04-18 ]. http ://ecfr. gpoacce. gov/cgi/text/text-idx? c = ecfr&tpl = % 2Dindex. tpl
  • 5FDA. CFR 21 Part 11, Electronic records & electronic signatures [OL]. 1997-03 [2009-04-18 ]. http ://ecfr. gpoaccess. gov/cgi/ t/text/text-idx? c = ecfr&tpl = % 2Findex. tpl
  • 6FDA. Guidance for industry: Part 11, Electronic records ; electronic signatures-validation [ OL]. 2001-08 [ 2009-04-18 ]. http ://www. fda. gov/cder/guidance/index. htm
  • 7FDA. Guidance for induatry: Part 11, electronic records; electronic signatures-time stamps[OL]. 2002-02 [ 2009-04-18 ]. http ://www. fda. gov/cder/guidance/index. htm
  • 8FDA. Guidance for industry: Part 11, electronic records ; electronic signatures-electronic copies of electronic records [ OL ]. 2002-08 [2009-04-18 ]. http://www. fda. gnv/cder/ guidance/ index. htm
  • 9FDA. Guidance for industry: Part 11, electronic records ; electronic signatures-maintenance of electronic records [ OL ]. 2002- 07 [ 2009-04-18 ]. http://www. fda. gov/cder/guidance/index. htm
  • 10FDA. Guidance for industry: Part 11, electronic records; electronic signatures-scope and application[ OL]. 2003-08[2009-04-18]. http://www. fda. gov/cder/guidance/index. htm

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