Provisions for Supervision and Administration of Medical Device Manufacturing

Promulgated by Decree No. 53 of the State Administration for Market Regulation on March 10, 2022
Provisions for Supervision and Administration of Medical Device Distribution

Promulgated by Decree No. 54 of the State Administration for Market Regulation on March 10, 2022
Provisions for Supervision and Administration of Manufacturing and Marketing of Cosmetics

Promulgated by Decree No. 46 of the State Administration for Market Regulation on August 2, 2021
Rules for Unique Device Identification System

The Rules shall be implemented as of October 1, 2019.
The Provisions for Registration and Filing of Cosmetics

Adopted at the 14th Executive Meeting of the State Administration for Market Regulation on December 31, 2020
Provisions for Medical Device Adverse Event Monitoring and Re-evaluation

Put into effect as of January 1, 2019