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Guidelines For Medical Device Usability Engineering Registration Review (March 19, 2024)

Application Note On Guideline For TheReview Of Medical Device Usability Engineering Registrations (October 8, 2024)

Guidelines For Review Of Medical Device Usability Engineering Registrations (March 27, 2024)

Guidelines For The Use Of Real-World Data In Clinical Evaluation Of Medical Devices-Trial(Nov 24, 2020)

Provisions For Drug Importation(January 1, 2004)

Drug Administration Law of The People’s Republic Of China(December 1, 2019)

Provisions For Instructions And Labels Of Medical Devices(October 1, 2014)

Provisions For Supervision Of Drug Distribution(May 1, 2007)

Provisions For Drug Insert Sheets And Labels(June 1, 2006)

Provisions For Drug Registration(July 1, 2020)

Provisions For The Supervision And Administration Of Drug Manufacturing(July 1, 2020)

Good Supply Practice For Drugs(June 30, 2016)