Drug >>Departmental Directives >>Adverse Drug Reaction
 
  • SFDA: Notification on Suspending the Use and the Review and Approval of 7 Injections such as Houttuynia Cordata Injection  (Directive; Document No: ShiYaoJianAn[2006]218; Promulgation Date: 2006-06-01)
  • SFDA: Notification on Explanations about Issues Concerning Reports of Regularly Collecting and Oversea Reports of Imported Adverse Drug Reaction  (Directive; Document No: GuoShiYaoJianAn[2005]89; Promulgation Date: 2005-2-25)
  • SFDA: Urgent Notification on Strengthening the Administration of Fluoride Foam Products  (Directive; Document No: GuoShiYaoJianXie[2004]132; Promulgation Date: 2004-04-27)
  • MOH: Notification on Promulgating Revised Draft of Traditional Chinese Medicine Prevention and Diagnostic Methods for SARS---the Part of Prevention  (Directive;Document No: WeiFeiDianFa[2003]2; Promulgation Date: 2003-04-23)
  • SDA: Notification on Issues Concerning the Usage of Mannan Peptide Injection  (Directive;Document No: GuoYaoJianAn[2003]24; Promulgation Date: 2003-01-24)
  • SDA: Urgent Notification on Supplementary Requirement for Clinical Research of Adaravone  (Directive;Document No: YaoJianZhuHan[2003]39; Promulgation Date: 2003-04-11)
  • SFDA: Notification on Suspending the Usage and Sale of Pharmaceutical Preparation Containing Phenylpropanolamine  (Directive;Document No: GuoYaoGuanBan[2000]523; Promulgation Date: 2000-11-14)
  • SDA: Notification on Issues Concerning Establishing Adverse Drug Reaction Reporting System  (Directive; Document No: GuoYaoJianAn[2001]487; Promulgation Date: 2001-11-19)
  • SDA and MOH: Notification on Promulgating Interim Provision for the Administration of Adverse Drug Reaction Monitoring  (Directive; Document No: GuoYaoGuanAn[1999]401; Promulgation Date: 1999-11-25)
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