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Announcement of NMPA on Recommended Application of 4 ICH Guidelines Including Q8 (R2): Pharmaceutical Development
2020-01-22
On January 21, 2020, NMPA issued a notice on recommending the application of ICH Guideline Q8 (R2): Pharmaceutical Development.
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Announcement of NMPA on Revising the Package Inserts of Drugs Containing Pipemidic Acid
2020-01-21
NMPA issued an announcement with decisions made to revise the [adverse reactions], [precautions] and other Entries on the package inserts of drugs containing pipemidic acid (including pipemidic acid tablets, capsules, and granules).
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Medical Device Unique Identification Database Goes Online
2019-12-10
In the next step, NMPA will strengthen guidance and services for the application of unique identification data for medical devices,and open the unique identification database query and sharing services to the pilot units in March 2020 in accordance with the pilot work deployments.
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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.
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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.
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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.
