The State Food and Drug Administration (SFDA) issued on Jan. 19, 2006 the requirements on daily supervision of the manufacturing of medical devices in accordance with Provisions for the Supervision of Medical Device Manufacturing to enhance the daily supervision of the manufacturing of medical devices and ensure the safety and effectiveness of medical devices.

Daily supervision of the manufacturing of medical devices includes quality system inspection, special inspection, product quality spot check and other daily on-site inspection, which will adopt graded responsibility system based on the jurisdiction