The food and drug inquiry platform is usually established and managed by relevant government departments or authoritative institutions to ensure the accuracy and authority of the information provided. Through this platform, the public can input information such as food and drug names, approval numbers or manufacturers to inquire and obtain detailed information of related products. This information helps consumers to know the source, quality and safety of products, so as to make more informed consumption choices.
The construction and operation of food and drug inquiry platform is of great significance for maintaining public health and safety. Through the inquiry platform, consumers can avoid buying counterfeit, expired or potential safety hazards, and reduce the health risks caused by food and drug problems. At the same time, the inquiry platform also provides convenience for the regulatory authorities, which can supervise the food and drug market more efficiently and protect the legitimate rights and interests of the public.
In order to ensure the accuracy and authority of the food and drug inquiry platform, the government and relevant institutions need to strengthen the supervision and maintenance of the platform. They should update the platform data regularly to ensure the timeliness and accuracy of information; At the same time, strengthen the publicity and education of platform users, and improve the public's query awareness and ability.
To sum up:
The food and drug inquiry platform is an important online service tool, which is convenient for the public to inquire about food and drug-related information and ensure public food and drug safety. The government and relevant institutions should strengthen the supervision and maintenance of the platform to ensure its accuracy and authority. The public should also actively use the inquiry platform to improve food and drug safety awareness and make wise consumption choices.
Legal basis:
People's Republic of China (PRC) Food Safety Law
Article 87 provides that:
The food safety supervision and administration department of the people's government at or above the county level shall conduct regular or irregular sampling inspection of food, and shall not be exempted from inspection. The food safety supervision and administration department of the people's government at or above the county level shall establish food safety credit files for food producers and operators, and record the issuance of licenses, the results of daily supervision and inspection, and the investigation and punishment of illegal acts. , and announced to the public according to law and updated in real time; Increase the frequency of supervision and inspection of food producers and operators with bad credit records, and notify the investment authorities, securities regulatory agencies and relevant financial institutions of food producers and operators with serious violations.
People's Republic of China (PRC) Drug Administration Law
Article 74 provides that:
Pharmaceutical producing enterprises, pharmaceutical trading enterprises and medical institutions must regularly check the quality, efficacy and response of drugs produced, marketed and used by their own units. Serious adverse reactions that may be related to drug use must be reported to the pharmaceutical supervisory and administrative departments and health administrative departments of the local people's governments of provinces, autonomous regions and municipalities directly under the Central Government in a timely manner. For the drugs produced by this unit, the observation period shall be stipulated according to the requirements of the drug supervision and administration department, and the samples during the observation period shall be kept.
People's Republic of China (PRC) Drug Administration Law
Article 85 provides that:
Pharmaceutical trading enterprises shall not give prescription drugs or Class A over-the-counter drugs to the public by tying, buying drugs as gifts or buying commodities as gifts. When selling drugs, pharmaceutical production enterprises and pharmaceutical trading enterprises shall issue sales vouchers indicating the name of the supplier, the name of the drug, the manufacturer, the batch number, the quantity and the price.