I, according to law, the implementation of drug approval and quality supervision and inspection of the required test.
Second, responsible for the province's drug manufacturers, business enterprises and medical institutions and other drug-related units of the quality of the implementation of technical supervision, registration and inspection, commissioned tests, supervision and sampling tests, re-inspection and arbitration, technical consulting;
Third, responsible for the province's drug testing vehicle technology promotion and application as well as on-board technical personnel business training and management;
Fourth, to undertake Experimental research on drug testing methods and related scientific research, as well as some of the national drug standards drafting, revision, review and other tasks;
V. Undertake the standardized products issued by the Institute of standard products, control products, collaborative calibration tasks;
Sixth, to undertake the grass-roots enterprises and institutions of the relevant personnel for further technical training, business training and internship of graduates of pharmaceutical institutions.
VII, food, health products, cosmetics and other testing.
VIII, the implementation of drug supervision and management departments assigned to the supervision and inspection of drugs and medical devices, pharmaceutical packaging materials and other related work.