Guizhou Province Drug Administration Functional Information
Guizhou Provincial Drug Administration to implement the Party Central Committee, the provincial party committee on drug supervision and management of the guidelines and policies and decision-making and deployment, in the course of performing their duties to adhere to and strengthen the Party's centralized and unified leadership of drug supervision and management work. The main responsibilities are:
(a) responsible for the supervision and management of drugs (including traditional Chinese medicine, ethnomedicine, the same below), medical devices and cosmetics safety. Organize the drafting of local laws and regulations, draft supervision and management policy planning, and supervise the implementation; organization and implementation of the management and service policies to encourage new technologies and products of drugs, medical devices and cosmetics.
(ii) Responsible for the management of drugs, medical devices and cosmetic standards. Supervise the implementation of the National Pharmacopoeia and other drugs, medical devices, cosmetics standards, supervise the implementation of the classification and management system. Cooperate with the implementation of the national basic drug system.
(C) is responsible for the registration of drugs, medical devices and cosmetics. Supervise the implementation of the registration management system in accordance with the provisions of the strict registration review and approval, improve the review and approval services to facilitate the implementation of measures and organizations.
(D) is responsible for the quality management of drugs, medical devices and cosmetics. Supervise the implementation of production quality management standards in accordance with the responsibilities. Supervision and guidance in accordance with the responsibilities of the implementation of business, the use of quality management standards.
(E) is responsible for drugs, medical devices and cosmetics post-market risk management. Organize and carry out monitoring, evaluation and disposal of adverse drug reactions, medical device adverse events and adverse reactions to cosmetics. Undertake emergency management of drugs, medical devices and cosmetics safety according to law.
(F) in accordance with the provisions of the registration of licensed pharmacists, management-related work.
(G) is responsible for the organization and implementation of drugs, medical devices and cosmetics supervision and inspection. In accordance with the duties to investigate and deal with drugs, medical devices and cosmetics registration, production, operation and other aspects of illegal behavior.
(H) is responsible for drugs, medical devices and cosmetics supervision and management of external exchanges and cooperation.
(IX) is responsible for guiding the city (state), county (city, district) drug supervision and management department.
(J) combined with departmental responsibilities, do a good job in military-civilian integration, poverty alleviation and development and other related work; increase investment in science and technology, improve scientific and technological innovation capacity, in order to promote innovation-driven development to provide protection; responsible for the department, the field of production safety and fire safety; according to the provisions of the development and application of big data and the management of governmental data resources related to the work of the department in accordance with the law to promote the standardization of governmental data resources management, sharing and openness.
(XI) to complete the provincial party committee, the provincial government and the State Drug Administration, the Provincial Market Supervision Bureau assigned other tasks.
