China to establish admission system for clinical pharmacists

Source: Internet
Author: User
Keywords Clinical pharmacist work China
BEIJING, January 10 (Xinhua) A spokesman for the Ministry of Health, Zhou Ting Deng 10th, said in a routine press conference that 2011 China will study the establishment of a clinical pharmacist admittance system and strengthen drug management in medical institutions. Deng in introducing the key points of health work in the 2011, we should strengthen the management of medical service and improve the quality of medical service. To promote the national medical quality Management and control center, key clinical specialized national medical quality and control center construction. We will continue to promote the mutual recognition of auxiliary examination results of the same level medical institutions and strengthen clinical application management of medical technology.  To identify and implement national clinical key specialist and key cultivation specialty construction projects to improve the medical service ability of our country. He also pointed to the need to strengthen the management of clinical use of medical devices. We should strengthen the construction and standardized management of pre-hospital care, and improve the ability of emergency emergency service. Standardize clinical examination work, increase hospital infection management, and ensure medical safety. Strengthen the construction of nurses team. To establish a long-term mechanism of unpaid blood donation to ensure blood quality and safety and clinical blood needs. Further promote medical rehabilitation, prevention and treatment of blindness and drug treatment management.  Strict examination and approval of medical advertisements and supervision. 2011, our country also must strengthen the drug quality safety supervision, guarantees the medicine quality safety. Strengthen the supervision of Drug Administration. To increase the supervision of the production and operation of pharmaceuticals and medical devices and to strengthen the capacity building of electronic supervision around the world. To strengthen the report and monitoring of adverse drug reactions, regularly analyze and evaluate ADR monitoring information, and control the risk of drug safety. To carry out the pilot work of the responsibility system of drug safety, establish and improve the local government-led drug safety responsibility system. Solid development of drug safety special rectification work. Strengthen the supervision of health food and cosmetics. Finish) (Editor: Lvjiang)
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