期刊文献+

美国仿制药制剂质量审评概况 被引量:2

下载PDF
导出
摘要 美国仿制药审评以坚实的法律法规和科学依据为基础。仿制药企业合理的设计生产,仿制药批准前后严谨的资料审评,以及严格的质量标准和现场考核都保证了仿制药的产品质量。
出处 《中国处方药》 2008年第10期43-46,共4页 Journal of China Prescription Drug
  • 相关文献

同被引文献20

  • 1梁云,邵蓉.美国仿制药管理的法制历程及其对我国的启示[J].食品与药品,2006,8(09A):67-69. 被引量:3
  • 2袁曙宏,张敬礼.百年FDA-美国药品监管法律框架[M].北京:中国医药科技出版社,2007.
  • 3王建英.美国药品申垠与法姆管理[M].北京:中国医药科技出版社,2005:195-197.
  • 4US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER). Guidance for industry: waiver of in vivo bioavailability and bioe- quivalence studies for immediate-release solid products, based on a biopharmaceutics classification system [EB/OL]. (2007-12- 17)[2010-01-12]. http: //www. fda. gov/cder/guidance/3618fnl. htm.
  • 5WHO. WHO expert committee on specifications for harmaceutical preparations: fortieth report; Annex 8: Proposal to waive in vivo bioequivalence requirements for WHO Model List of Essential Medicines immediate-release, solid oral dosage forms [EB/OL]. (2008-12-15 ) [2010-01 - 12 ]. http : //whqlibdoc. who. int/trs/ WHO TRS 937 eng. pdf.
  • 6European Medicines Agency. Committee for proprietary edicinal products. Note for guidance on the investigation of bioequivalence [EB/OL]. (2008-07-24)[2010-01-12]. http: //www. emea. europa, eu/pdfs/human/qwp/140198enfin, pdf.
  • 7International Conference on Harmonisation. ICH harmonised tripar tite guideline: pharmaceutical development Q8 (R2) [EB/OL] (2008-07-24) [2010-03-19]. http: //www. ich. org/LOB/media/MEDIA4986, pdf.
  • 8US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER) Abbreviated new drug applications (ANDA) : generics [EB/OL] (2009-11-24) [2010-01-15]. http ://www. fda. gov/cder/ogd/.
  • 9国家食品药品监督管理局药品审评中心.药品审评中心颁布《关于同步对外公布中心拟研究共性问题的管理办法(暂行)》[EB/OL].(2006-01-24)[2010-3-29].http://www.cde.org.cn/news.do?method=largeInfo&id=492.
  • 10US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research(CDER). Manual of policies & procedures, chapter 5200-generic drugs[EB/ OL]. (2007-07-16)[2010-03-29]. http: //www. fda. gov/About FDA/CentersOffices/CDER/ManualofPoliciesProcedures/defauh. htm#generic.

引证文献2

二级引证文献36

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部