NMPA Announces New and Revised Catalogues of Medical Devices Exempted from Clinical Trials

2019-12-20

NMPA organized the formulation of new and revised catalogs (omitted) of medical devices and in vitro diagnostic reagents exempt from clinical trials, which have been announced on December 20, 2019.

NMPA Issued the Guidelines for Conditional Approval for Marketing of Medical Devices

2019-12-20

NMPA organized the formulation of and released on December 20, 2019 the Guidelines for Conditional Approval for Marketing of Medical Devices.

NMPA Issued the Guidelines for Nomenclature for Common Names of Medical Devices

2019-12-25

NMPA has organized the formulation of the Guidelines for Nomenclature for Common Names of Medical Devices, which has been issued on December 25, 2019.

NMPA Issued Four Guidelines for Technical Review of the Registration of Assay Reagents for Aspartate Aminotransferase and Others

2019-10-29

NMPA Issued Three Guidelines for Technical Review of the Registration of Embryo Replacement Catheter in Assisted Reproduction and Others

2019-11-01

NMPA Announcement on the Issuance of 21 Medical Device Industry Standards such as YY / T 0464-2019 Single-Use Hemoperfutor and 1 Modification Order

2019-11-13