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Interpretation of 《Regulations on the Supervision and Administration of Enterprises’ Responsibility
2022-12-30 -
Instuctions of <Guiding Principles for Naming Recombinant Collagen biomaterials>
2023-02-01 -
CMDE: Notice on Further Clarifying Matters Related to the Filing and Use of Device Master File
2023-01-31 -
NMPA Announcement on Delaying the Payment of Registration Fees for Drugs and Medical Devices
2022-09-30 -
NIFDC Notice on Soliciting Opinions on Revision of YY 0649-2016 Medical Device Industry Standard No.
2022-09-19 -
NMPA Interpretation of Medical Device Recall Management Measures
2022-04-12 -
NMPA Interpretation of "Quality Management Practice for Medical Device Clinical Trials"
2022-04-01 -
CMDE issues current considerations for claiming "antibacterial and antiviral" masks
2022-03-15 -
Jiangsu MPA's application for the registration of Class II medical devices Reminders about matters
2022-02-28 -
Explanation of "Classification Rules for In Vitro Diagnostic Reagents"
2022-01-19
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