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Latest Regulations

1061  Results

Notice of the National Medical Products Administration on Issuing the Guiding Principles for the Review of Two Registration Technologies, including CYP2C19 Drug Metabolizing Enzyme Gene Polymorphism Detection Reagents
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2019年第83号-f2 Registration & Filing 2019-12-05 2019-11-12
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines IVD
Notice of the National Medical Products Administration on Issuing the Guiding Principles for the Review of Five Registration Technologies, including Human Chromosome Abnormality Detection Reagents Based on Cell Fluorescence in situ Hybridization
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2019年第80号-f1 Registration & Filing 2019-11-15 2019-11-01
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines IVD
Notice of the National Medical Products Administration on Issuing the Guiding Principles for the Review of Five Registration Technologies, including Respiratory Virus Multiple Nucleic Acid Testing Reagents
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2019年第80号-f2 Registration & Filing 2019-11-15 2019-11-01
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines IVD
Notice of the National Medical Products Administration on Issuing the Guiding Principles for the Review of Five Registration Technologies, including Nucleic Acid Testing Methods for Staphylococcus aureus and Methicillin Resistant Staphylococcus aureus Testing Reagents
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2019年第80号-f3 Registration & Filing 2019-11-15 2019-11-01
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines IVD
Notice of the National Medical Products Administration on Issuing the Guiding Principles for the Review of Five Registration Technologies, including Chlamydia trachomatis and/or Neisseria gonorrhoeae Nucleic Acid Testing Reagents
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2019年第80号-f4 Registration & Filing 2019-11-15 2019-11-01
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines IVD
Notice of the National Medical Products Administration on Issuing the Guiding Principles for the Review of Five Registration Technologies, including Amino Acids, Carnitine, and Succinyl Acetone Testing Reagents
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2019年第80号-f5 Registration & Filing 2019-11-15 2019-11-01
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines IVD
Notice of the National Medical Products Administration on Issuing 13 Guiding Principles for Registration Technical Review of Limb Pressure Therapy Equipment and Other Devices
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2019年第79号-f1 Registration & Filing 2019-11-15 2019-11-01
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Notice of the National Medical Products Administration on Issuing 13 Guiding Principles for Registration Technical Review, including Direct Ophthalmology
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2019年第79号-f3 Registration & Filing 2019-11-15 2019-11-01
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Notice of the National Medical Products Administration on Issuing 13 Registration Technical Review Guidelines for Medical Diagnostic X-ray Tube Components and Other Components
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2019年第79号-f4 Registration & Filing 2019-11-15 2019-11-01
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
Notice of the National Medical Products Administration on Issuing the Guiding Principles for the Review of 13 Registration Technologies, including Electromyography Biofeedback Therapy Devices
Regulation No. Product LifeCycle Issued Date Implemented Date 国药监局通告2019年第79号-f5 Registration & Filing 2019-11-15 2019-11-01
Status Issued By Level of Legal Effect Product Category Valid NMPA/National Medical … Guidelines Medical Device
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