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Latest Regulations

1153  Results

Guiding Principles for Clinical Evaluation, Registration and Review of the Same Variety of Spring Coil Systems (Draft for Comments)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20231211-3 Registration & Filing 2023-12-11 2023-12-11
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines Medical Device
Guidelines for Clinical Trial Registration and Review of Facial Injection Filler Materials (Draft for Comments)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20231211-4 Registration & Filing 2023-12-11 2023-12-11
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines Medical Device
Notice on Public Solicitation of Opinions on the Guiding Principles for Registration and Review of High Frequency Surgical Instruments for Soft Endoscopes (Draft for Solicitation of Opinions)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20231206 Registration & Filing 2023-12-06 2023-12-05
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines Medical Device
Notice of the Equipment Review Center of the National Medical Products Administration on Issuing the Guiding Principles for Registration and Review of Extracorporeal Membrane Oxygen (ECMO) Loop Animal Trials (No. 39 of 2023)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE通告2023年第39号 Registration & Filing 2023-12-06 2023-12-05
Status Issued By Level of Legal Effect Product Category Valid CMDE/Center for … Guidelines Medical Device
Guiding Principles for Clinical Evaluation, Registration and Review of Individualized Drug Genetic Testing Reagents (Draft for Comments)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20231206-1 Registration & Filing 2023-12-06 2023-12-06
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines IVD
Guidelines for Registration and Review of HLA-B27 Genetic Testing Reagents (Draft for Comments)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20231206-2 Registration & Filing 2023-12-06 2023-12-06
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines IVD
Guidelines for Clinical Trial Registration and Review of Colorectal Cancer Related Gene Methylation Detection Kit (Draft for Comments)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20231206-3 Registration & Filing 2023-12-06 2023-12-06
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines IVD
Guidelines for Registration and Review of ALDH2 Gene Polymorphism Testing Reagents (Draft for Solicitation of Comments)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20231201-1 Registration & Filing 2023-12-01 2023-12-01
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines IVD
Guidelines for Registration and Review of Antibiotic Drug Sensitivity Testing Reagents (Draft for Comments)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20231201-2 Registration & Filing 2023-12-01 2023-12-01
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines IVD
Guidelines for Registration and Review of Human MTHFR Gene Polymorphism Testing Reagents (Draft for Solicitation of Comments)
Regulation No. Product LifeCycle Issued Date Implemented Date CMDE-20231201-3 Registration & Filing 2023-12-01 2023-12-01
Status Issued By Level of Legal Effect Product Category Draft CMDE/Center for … Guidelines IVD
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