SFDA carries out catalogue management to the production of some export drugs and medical devices

According to the requirements of the Announcement on Implementing Catalogue Management to the Production of Some Export Drugs and Medical Devices issued by the State Food and Drug Administration (SFDA), the catalogue management has been practiced to the production of some export drugs and medical devices since October 18, 2010. To the products included in the Product Catalogue for Export Drugs and Medical Devices Supervision, SFDA recently released the list of drug manufacturing enterprises that have obtained the Drug Manufacturing Certificate and the drug approval number, and the list of medical device manufacturing enterprises that have obtained the Medical Device Manufacturing Enterprise License and the Medical Device Registration Certificate.

source： SFDA