Legal analysis: the hospital charter should include the nature of the hospital, the purpose of running a hospital, functional positioning, the direction of running a hospital, the management system, the source of funding, organizational structure, decision-making mechanism, management system, supervision mechanism, cultural construction, party construction, group construction, as well as organizing the main body, the hospital, the rights and obligations of the staff and other content.
(1) the nature of the hospital: mainly refers to non-profit and for-profit
(2) the purpose of running the hospital: the purpose of public hospitals is to serve the people's health
(3) functional positioning: the hospital is in the three-tier health care network in what position, is a few levels of hospitals, is a regional medical centers, specialty hospitals or community-based basic health care, the main provision of what basic medical and health services, etc.
(4) the direction of the hospital: refers to what kind of hospital, is a general hospital, or Chinese medicine hospital, or specialty hospitals, key specialties and professional characteristics are what.
(5) management system: mainly refers to the relationship between the management and the office, whether to set up a medical management center, or the establishment of the Council, or the establishment of the Board of Directors, detailed list of powers and responsibilities of the Government and the hospital.
Legal basis: "Chinese People's **** and the State Drug Administration Law"
Article 1 In order to strengthen the management of medicines, to ensure the quality of medicines, to ensure the safety of the public medicines and legitimate rights and interests, and to protect and promote public health, the enactment of this law.
Article 2 This Law shall apply to the development, production, operation, use and supervision and management of medicines within the territory of the People's Republic of China*** and the People's Republic of China.
Drugs referred to in this Law are substances, including traditional Chinese medicines, chemical medicines and biological products, which are used for the prevention, treatment and diagnosis of human diseases, and for the purpose of regulating human physiological functions, as well as providing for indications or functional prescriptions, usage and dosage.
Article 3 The management of medicines shall be centered on people's health, adhere to the principles of risk management, whole process control and social ****governance, establish a scientific and strict supervision and management system, comprehensively improve the quality of medicines, and safeguard the safety, efficacy and accessibility of medicines.
Article 4 The State develops modern and traditional medicines, giving full play to their role in prevention, medical treatment and health care.
The State protects the resources of wild medicinal herbs and varieties of traditional Chinese medicine, and encourages the cultivation of authentic Chinese medicinal herbs.
Article 5 The State encourages the research and creation of new medicines, and protects the lawful rights and interests of citizens, legal persons and other organizations in the research and development of new medicines.
Article 6 The State implements the system of drug marketing authorization holders for drug management. The holder of the marketing authorization of drugs in accordance with the law on the development, production, operation and use of drugs in the whole process of drug safety, effectiveness and quality control.
Article VII engaged in the development, production, operation and use of drugs, shall comply with laws, regulations, rules, standards and norms, to ensure that the whole process of information is true, accurate, complete and traceable.
Article 8 The State Council Drug Administration is in charge of the supervision and management of national drug supervision and management work. The relevant departments of the State Council in their respective areas of responsibility for supervision and management work related to drugs. Drug supervision and management department of the State Council with the relevant departments of the State Council, the implementation of the national drug industry development planning and industrial policy.
The drug supervision and management departments of the people's governments of the provinces, autonomous regions and municipalities directly under the Central Government are responsible for the supervision and management of drugs in their own administrative regions. Municipal and county people's governments are responsible for the supervision and management of drug supervision and management departments (hereinafter referred to as drug supervision and management department) is responsible for the supervision and management of drugs in the administrative area. The relevant departments of the local people's governments at or above the county level are responsible for the supervision and management of drugs within their respective areas of responsibility.