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Issuance date

  • 2016
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  • 2009
  • before2008

RegDoc.

  • Main Enabling Legislation
  • Registration
  • Classification
  • Manufacture
  • Distribution
  • Use
  • Import/Export
  • QMS
  • Clinical Verification
  • Labeling/Packaging
  • Adverse Event Monitoring
  • Reevaluation/Recall
  • Administrative Supervision
  • Medical Device Inventory
  • Regulations
  • 2015 Administrative-Supervision
  • Measures for Unannounced Inspection of Drugs and Medical Devices (CFDA Order No.14 2015)
  • 2013 Administrative-Supervision
  • Administrative provisions for medical device quality supervision and spot check(Exposure Draft)(CFDA notice No. 46 2013)
  • 2014 Administrative-Supervision
  • Administrative Measures for Medical Device Supervision Inspector (Exposure Draft)(CFDA notice No. 129 2014)
  • 2012 Administrative-Supervision
  • The Applicable Rules on Administrative Punishment Discretion for Drug and Medical Device(SFDA notice No.306 2012)
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