Advocacy Actions
Conclusion Meeting on the Recycling and Remanufacturing of High-end Medical Imaging Equipment
Conclusion Meeting on the Recycling and Remanufacturing of High-end Medical Imaging Equipment
Read moreComments to NMPA's Public Consultation on the Classification Rules for In Vitro Diagnostics
The medical devices sector sent comments to the National Medical Products Administration's public consultation on the Classification Rules for In Vitro Diagnostics.
Read moreComments to NMPA's Public Consultation on the In-Vitro Diagnostic Reagent Registration Application Data Requirements and Approval Document Format
The medical devices sector sent comments to the National Medical Products Administration's (NMPA) public consultation on the In-Vitro Diagnostic Reagent Registration Application Data Requirements and Approval Document Format.
Read moreComments to NMPA's Pulic Consultation on the Medical Device Registration Application Data Requirements and Approval Document Format
The medical devices sector sent comments to the National Medical Products Administration's (NMPA) public consultation on the Medical Device Registration Application Data Requirements and Approval Document Format.
Read moreComments to NMPA's Public Consultation on the Category of Medical Devices Exempeted from Clinical Evalutaion
The medical devices sector sent comments to the National Medical Products Administration's (NMPA) public consultation on the Category of Medical Devices Exempeted from Clinical Evalutaion.
Read moreComments to NMPA's Public Consultation on the Technical Guideline for Methodological Comparison Of In Vitro Diagnostic Reagents Free of Clinical Trials
The medical devices sent comments to the National Medical Products Administration's (NMPA) public consultation Technical Guideline for Methodological Comparison Of In Vitro Diagnostic Reagents Free of Clinical Trials.
Read moreComments to NMPA's Public Consultation on the Techinal Guidelines for Clinical Evaluation Report for Medical Device Registration
The medical devices sector sent comments to the National Medical Products Administration's (NMPA) public consultation on the Techinal Guidelines for Clinical Evaluation Report for Medical Device Registration.
Read moreComments to NMPA's Public Consultation on the Technical Guidelines for Deciding Whether to Conduct Medical Devices Clinical Trails
The medical devices sector sent comments to the National Medical Products Administration's (NMPA) on the Technical Guidelines for Deciding Whether to Conduct Medical Devices Clinical Trails.
Read moreComments to NMPA's Public Consultation on the Technical Guidelines for Medical Devices Equivalence Demonstration
The medical devices sector sent comments to the National Medical Producst Administration's (NMPA) public consultation on the Technical Guidelines for Medical Devices Equivalence Demonstration.
Read moreComments to NMPA's Public Consultation on the Technical Guideline for Medical Devices Clinical Evaluation
The medical devices sector sent comments to the National Medical Products Administration's (NMPA) public consultation on the Technical Guideline for Medical Devices Clinical Evaluation.
Read more