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  • The procedure for Import Drug SFDA Registration
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  • China Launches Review of Medical Device Industry
  • The drugs which can be exempted from clinical trials in China
  • CFDA Reduces Application Requirements for Medical Device License Amendment and Renewal Processes
  • CFDA Issues Guide for Routine Inspections of Medical Device Manufacturers
  • CFDA Issues Proposed Regulations on Medical Devices
  • China Hygiene Supervision and Inspection of Food
  • Application and approval procedure for clinical trials
  • Our Services for IPEL (Import pharmaceutical excipient Licence)
  • China Import Control on GM Agricultural Bioproducts
  • Requisite documents of Drugs SFDA Registration
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    Latest Articles
  • China Hygiene Supervision and Inspection of Food
  • China Supervision and Inspection of Drugs
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  • China Import Control on GM Agricultural Bioproducts
  • China Customs Clearance for Goods Subject to Entry-exit Inspection and Quarantine
  • What is AQSIQ of China?
  • China Issues Special Procedures for Innovative Medical Devices
  • CFDA Issues Guide for Routine Inspections of Medical Device Manufacturers
  • CFDA Releases Draft Good Supply Practices for Medical Devices
  • CFDA Reduces Application Requirements for Medical Device License Amendment and Renewal Processes
  • CFDA Releases Plan to Improve Medical Device Adverse Event Monitoring
  • China Launches Review of Medical Device Industry
  • China Reorganizes the State Food and Drug Administration and Appoints a New Commissioner
  • China FDA Seeks to Improve Medical Device Evaluation at the Provincial and Municipal Government Levels
  • CFDA Publishes Draft Rule on Administrative Procedure for Public Comment
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