Home
Regulatory Database
Learning Portal
About Us
Contact Us
English
English
简体中文
Log in
Sign Up
Regulation Title
Regulation NO
Product Life Cycle
Pre-Market
Product Type Testing
Clinical Evaluation
Registration & Filing
Manufacturing
Distribution
Usage
Supervision & Inspection
Search
FILTER
Product Life Cycle
Pre-Market
Product Classification
Labeling & UDI
Product R&D
Innovative Medical Devices
Naming Rules
Developing Experiments
Registration Units
IFU & Labeling
Product Type Testing
Product Techincial Requirements
Product Registration Testing
Testing Centers
Self Testing
Standards
Clinical Evaluation
Clinical Trial Site
IVD Clinical Evaluation
Clinical Trial
Medical Device Clinical Evaluation
Ethical Review
GCP
Clinical Evaluation Exemption
Registration & Filing
Certificate Issuance
Registration Dossier
Reviewing Process
Registration Issues
Efiling (eRPS)
Application Acceptance
Fliing Review
Supplmental Phase
Pre-review
Services of Documents
Registration Fees
QMS Inspection
Master Files
Expert Consultation
NMPA Consultation
Prioriity Approval
Conditional Approval
Urgent Approval
IFU & Labeling
Online Application
Manufacturing
Application Acceptance
Certificate Issuance
GMP
Contract Manufacturing
Distribution
Application Acceptance
Certificate Issuance
GSP
Advertisement
Recall
Usage
Usage Management
Disposable Medical Devices
Adverse Events
Supervision & Inspection
Regulator
Penalties
Insepction Plan
Insepctor
Inspection Results
Management Practices
Status
Vaild
Draft
Obsolete
Level of Legal Effect
Law
Administrative Regulations
Departmental Rules
Normative Documents
Announcements
Work Documents
Guidelines
Review Key Points
Product Categories
Medical Device
Combination Product
Non-Medical Device
IVD
IVD Regulated as Pharmaceuticals
Issuing Organization
CMDE/Center for Medical Device Evaluation
NMPA/National Medical Products Administration
NIFDC/National Institutes for Food and Drug Control
Center for Medical Device Standardization Administration
Ministry of Justice of the Peoples Republic of China
State Council of the People's Republic of China
National Heath Commission of the People's Republic of China
Ministry of Science and Technology of the People’s Republic of China
Ministry of Finance of the People’s Republic of China
National Health Security Administration
SAMR/State Administration for Market Regulation
Latest Regulations
42 Results
Sort By
Issue Date
Newest
Oldest
Title
ASC
DESC
Notice on Issuing Guiding Principles for Clinical Evaluation and Registration Technical Review of Centrifugal Blood Component Separation Equipment
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
国药监局通告2019年第24号
Clinical Evaluation
2019-05-15
2019-05-10
Status
Issued By
Level of Legal Effect
Product Category
Valid
NMPA/National Medical …
Guidelines
Medical Device
Notice on Public Solicitation of Comments on the Draft Results Document of the "Clinical Trial" Coordination Project
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE-20190412-5
Clinical Evaluation
2019-04-12
2019-04-12
Status
Issued By
Level of Legal Effect
Product Category
Draft
CMDE/Center for …
Work Documents
Medical Device
Notice on soliciting public opinions on the draft outcome document of the "Clinical Evaluation of Medical Devices" coordination project
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE-20190412-3
Clinical Evaluation
2019-04-12
2019-04-12
Status
Issued By
Level of Legal Effect
Product Category
Draft
CMDE/Center for …
Work Documents
Medical Device
Notice on Issuing Four Guiding Principles for Clinical Evaluation of Oral and Maxillofacial Cone Beam Computed Tomography Equipment
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
国药监局通告2019年第10号-f4
Clinical Evaluation
2019-03-26
2019-02-28
Status
Issued By
Level of Legal Effect
Product Category
Valid
NMPA/National Medical …
Guidelines
Medical Device
Notice on soliciting opinions on the draft guidelines for animal experiments and clinical evaluation of implantable sacral nerve stimulation systems
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
CMDE-20180927-3
Clinical Evaluation
2018-09-27
2018-09-27
Status
Issued By
Level of Legal Effect
Product Category
Draft
CMDE/Center for …
Guidelines
Medical Device
Notice of the National Medical Products Administration on Issuing the Preclinical Research Guidelines for Coronary Artery Drug eluting Stents
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
国药监局通告2018年第21号-f1
Clinical Evaluation
2018-05-11
2018-05-04
Status
Issued By
Level of Legal Effect
Product Category
Valid
NMPA/National Medical …
Guidelines
Combination Product
Notice of the National Medical Products Administration on Issuing the Guiding Principles for Clinical Trials of Coronary Artery Drug eluting Stents
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
国药监局通告2018年第21号-f2
Clinical Evaluation
2018-05-11
2018-05-04
Status
Issued By
Level of Legal Effect
Product Category
Valid
NMPA/National Medical …
Guidelines
Combination Product
Notice of the State Administration on Issuing Technical Guidelines for Accepting Overseas Clinical Trial Data of Medical Devices
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
总局公告2018年第13号
Clinical Evaluation
2018-01-11
2018-01-11
Status
Issued By
Level of Legal Effect
Product Category
Valid
NMPA/National Medical …
Guidelines
IVD
Notice of the State Administration on Issuing the Guiding Principles for Clinical Evaluation Technology Review of Proton Carbon Ion Therapy Systems
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
总局通告2018年第4号
Clinical Evaluation
2018-01-08
2018-01-04
Status
Issued By
Level of Legal Effect
Product Category
Valid
NMPA/National Medical …
Guidelines
Medical Device
Notice of the State Administration on Issuing the Guiding Principles for the Review of Two Clinical Evaluation Techniques, including Endometrial Removal (Heat Conduction, Radiofrequency Ablation) Equipment
Regulation No.
Product LifeCycle
Issued Date
Implemented Date
总局通告2017年第212号-f2
Clinical Evaluation
2017-12-22
2017-12-18
Status
Issued By
Level of Legal Effect
Product Category
Valid
NMPA/National Medical …
Guidelines
Medical Device
«
1
2
3
4
5
»
×