To conduct research on important policies on drug, medical devices and cosmetics regulation; to organize the drafting of laws, regulations and provisions; to examine and verify the legality of normative documents; to undertake the supervision of law enforcement, administrative reconsideration, administrative respondence and legal review of important cases; to undertake the management of the connection between administrative enforcement and criminal justice; to carry out popularizing-law education and work related to WTO; to be responsible for related coordination for comprehensively deepening reform; to undertake routine work of Vaccine Quality Management System (QMS) Office.

1) Division of General Affairs

2) Division of Policy Research

3) Division of Regulations

4) Division of Enforcement Supervision