Notice of CFDA on Adjusting the On-site Inspection Procedures for the Production of Invitro Diagnostic Reagents Under Drug Management
Request Notice of CFDA on Adjusting the On-site Inspection Procedures for the Production of Invitro Diagnostic Reagents Under Drug Management
  • Local Title:国家食品药品监督管理局办公室关于调整按药品管理的体外诊断试剂生产现场检查程序的通知
  • Country/Region:Chinese Mainland
  • Competent Authority: Former China Food and Drug Administration (CFDA)
  • Type:Notice
  • Status:In force
  • Release Date:2012-06-29
  • Implementation Date:2012-06-29
Document
Language Source Title Access
ZH Official 国家食品药品监督管理局办公室关于调整按药品管理的体外诊断试剂生产现场检查程序的通知 Download
Summary

The Notice of CFDA on Adjusting the On-site Inspection Procedures for the Production of Invitro Diagnostic Reagents Under Drug Management was issued on Jun.29, 2012. It includes  relevant policies, regulations, and measures.