[State Food and Drug Administration: Upgrading the supervision of the entire chain of drug safety] On September 20, Yang Sheng, deputy director of the State Food and Drug Administration, said at a press conference of the State Council Information Office that during the "15th Five-Year Plan" period, opinions on improving the drug safety responsibility system will be issued, and the revision of laws and regulations such as the Medical Device Management Law and the Regulations on the Protection of Traditional Chinese Medicine Variety will be promoted. Comprehensively implement the Implementation Regulations of the Drug Administration Law, improve supporting systems, implement an action plan to improve drug and medical device standards, compile the 2030 version of the Chinese Pharmacopoeia, give priority to the inclusion of essential drugs, medical insurance drugs and high-risk preparation varieties, strengthen the research and formulation of standards in cutting-edge fields such as brain-computer interfaces, and drive quality improvement through standard upgrades.