Main responsibilities of Liaoning Provincial Drug Administration

        I. Responsible for the safety supervision and administration of drugs (including traditional Chinese medicine, ethnic medicine, the same below), medical devices and cosmetics。To carry out the national laws and regulations on the safety supervision and administration of drugs, medical devices and cosmetics, organize the drafting of relevant local regulations and provincial government regulations as well as policy planning and supervise the implementation。To study and formulate management and service policies to encourage new technologies and products of pharmaceuticals, medical devices and cosmetics。
        Ii. Responsible for the standard management of drugs, medical devices and cosmetics。To supervise the implementation of standards and classification management systems for drugs, medical devices and cosmetics, promulgation and implementation of local TCM processing standards, and cooperate with relevant departments to implement the national essential drugs system。
        Iii. Responsible for the registration management of drugs, medical devices and cosmetics。To be responsible for the registration, supervision and inspection of drugs, medical devices and cosmetics, and organize the implementation of the registration of licensed pharmacists。Responsible for the administrative licensing and filing of drugs, medical devices and cosmetics production, drug wholesale licensing, retail chain headquarters licensing, Internet sales third-party platform filing。
        Iv. Responsible for the quality management of drugs, medical devices and cosmetics。To supervise the implementation of quality management standards for drug research, production and marketing, to supervise the implementation of quality management standards for medical device research and production, and to supervise the implementation of hygiene standards and technical standards for cosmetics production。
        V. Responsible for post-marketing risk management of drugs, medical devices and cosmetics。To organize the monitoring, evaluation and disposal of adverse drug reactions, adverse events of medical devices and adverse reactions of cosmetics, and to undertake the safety emergency management of drugs, medical devices and cosmetics according to law。
        6. Responsible for organizing and implementing supervision and inspection of drugs, medical devices and cosmetics。Formulate inspection systems, investigate and punish illegal activities in the production of drugs, medical devices and cosmetics, drug wholesale, drug retail chain headquarters, and third-party platforms for Internet sales, and supervise the implementation of problem product recall and disposal systems。Organize and guide the investigation and punishment of illegal acts in other links according to their duties。
        7. Complete other tasks assigned by the Provincial Party Committee and the provincial government。