The main responsibilities of the National Pharmacopoeia Committee are as follows

Legal analysis: the main responsibilities of the National Pharmacopoeia Committee;

(1) Organizing the compilation, revision and assembly of People's Republic of China (PRC) Pharmacopoeia (hereinafter referred to as China Pharmacopoeia) and its supporting standards.

(2) Organizing the formulation and revision of national drug standards. Participate in the formulation of relevant drug standard management system and working mechanism.

(3) Organizing the selection of medicinal varieties listed in China Pharmacopoeia. Responsible for naming the generic names of drugs.

(four) to organize the implementation and evaluation of China Pharmacopoeia and national drug standards.

(five) to carry out research on the development strategy, management policy and technical regulations of drug standards. Undertake the informatization construction of drug standards.

(six) to carry out international (regional) coordination and technical exchange of drug standards, and to participate in international (regional) cooperation in drug standard certification.

(seven) to organize the publicity, training and technical consultation of China Pharmacopoeia and national drug standards, and to be responsible for the editing and publishing of drug standards of china and other publications.

(eight) responsible for the organization, coordination and service guarantee of the professional committees of the Pharmacopoeia Committee.

(nine) to undertake other tasks assigned by the State Council.

Legal basis: Drug Administration Law of People's Republic of China (PRC).

Eleventh pharmaceutical professional and technical institutions established or designated by the pharmaceutical supervisory and administrative departments shall undertake the review, inspection, verification, monitoring and evaluation required for the implementation of pharmaceutical supervision and administration according to law.

Article 12 The State shall establish and improve the drug traceability system. The drug supervision and administration department of the State Council shall formulate unified standards and norms for drug traceability, promote the mutual sharing of drug traceability information, and realize drug traceability.

The state establishes a pharmacovigilance system to monitor, identify, evaluate and control adverse drug reactions and other harmful reactions related to drug use.