Legal analysis: Medical oxygen management system Medical oxygen management system According to the relevant regulations of the Ministry of Health: Medical oxygen (including liquid oxygen and gaseous oxygen) is managed by drug approval number; The procurement and management of medical oxygen should be brought into the pharmacy department of each hospital, in strict accordance with drug management. 1. Purchase and acceptance of medical oxygen: 1. To purchase medical oxygen, the medical oxygen with the approval number shall be purchased from the production enterprise with Pharmaceutical Production License and Pharmaceutical GMP Certificate or the business enterprise with Pharmaceutical Business License and Pharmaceutical GSP Certificate, and the quality of medical oxygen shall meet the requirements of national standards.
Legal basis: Drug Administration Law of the People's Republic of China
Article 4 The state develops modern and traditional medicines and gives full play to their roles in prevention, medical treatment and health care.
the state protects wild medicinal resources and varieties of Chinese medicines, and encourages the cultivation of authentic Chinese medicines.
article 5 the state encourages the research and creation of new drugs and protects the legitimate rights and interests of citizens, legal persons and other organizations in the research and development of new drugs.
article 6 the state implements the system of drug marketing license holders for drug management. The holder of drug marketing license is responsible for the safety, effectiveness and quality controllability of drugs in the whole process of drug development, production, management and use according to law.
article 7 in drug research, production, marketing and use, laws, regulations, rules, standards and norms shall be observed to ensure that the information in the whole process is true, accurate, complete and traceable.
article 8 the drug supervision and administration department of the State Council is in charge of drug supervision and administration throughout the country. The relevant departments of the State Council are responsible for the supervision and administration of drugs within their respective responsibilities. The drug supervision and administration department of the State Council cooperates with the relevant departments of the State Council to implement the national drug industry development plan and industrial policy.
the pharmaceutical supervisory and administrative departments of the people's governments of provinces, autonomous regions and municipalities directly under the central government are responsible for the pharmaceutical supervisory and administrative work within their respective administrative areas. The departments responsible for drug supervision and administration of the people's governments at the municipal and county levels divided into districts (hereinafter referred to as drug supervision and administration departments) shall be responsible for drug supervision and administration within their respective administrative areas. The relevant departments of the local people's governments at or above the county level shall be responsible for the supervision and administration of drugs within the scope of their respective duties.
article 9 the local people's governments at or above the county level shall be responsible for the drug supervision and administration within their respective administrative areas, uniformly lead, organize and coordinate the drug supervision and administration within their respective administrative areas and the response to drug safety emergencies, and establish and improve the drug supervision and administration working mechanism and information sharing mechanism.
article 1 the people's governments at or above the county level shall incorporate drug safety work into the national economic and social development plan at the corresponding level, include the funds for drug safety work in the government budget at the corresponding level, strengthen the capacity building of drug supervision and management, and provide guarantee for drug safety work.
article 11 the pharmaceutical professional technical institutions set up or designated by the pharmaceutical supervisory and administrative departments shall undertake the review, inspection, verification, monitoring and evaluation required for the implementation of pharmaceutical supervision and administration according to law.
article 12 the state establishes and improves the drug traceability system. The drug supervision and administration department of the State Council shall formulate unified standards and norms for drug traceability, promote the mutual sharing of drug traceability information, and realize drug traceability.
the state establishes a pharmacovigilance system to monitor, identify, evaluate and control adverse drug reactions and other harmful reactions related to drug use.
Article 13 People's governments at all levels and their relevant departments, pharmaceutical industry associations, etc. shall strengthen the publicity and education on drug safety and carry out the popularization of drug safety laws and regulations.
the news media should carry out public welfare publicity on the knowledge of drug safety laws and regulations, and supervise drug violations by public opinion. The publicity and reporting on drugs should be comprehensive, scientific, objective and fair.
article 14 pharmaceutical industry associations shall strengthen industry self-discipline, establish and improve industry norms, promote the construction of industry credit system, and guide and urge members to carry out activities such as pharmaceutical production and operation according to law.
article 15 the people's governments at or above the county level and their relevant departments shall commend and reward the units and individuals that have made outstanding contributions in the research, production, marketing, use, supervision and management of drugs in accordance with the relevant provisions of the state.