Electronic drug regulatory code
As a well-known intelligent automation equipment research and development enterprise at home and abroad, Shanghai Lujia Automation Technology Co., Ltd. provides technical solutions for the Chinese manufacturing industry to synchronize with the international electronic drug regulatory code technology. Widely used in: pharmaceutical, food, beverage, daily chemical, health care products, electronics, electrical appliances, chemicals, automotive industry and plastics and hardware industries!
The drug electronic supervision code management system is aimed at the state supervision of drugs in the process of production and circulation, realizing the traceability and management of products of the regulatory authorities and production enterprises, and safeguarding the legitimate rights and interests of drug manufacturers and consumers. Relying on the national drug supervision network platform covering the whole country to complete product status inquiry, traceability and management functions.
1. The entire process from production, distribution, transportation, storage to distribution to medical institutions is under the supervision of the drug regulatory authority.
2. Real-time query of the production, operation, inventory and flow direction of each box, each box and each batch of key drugs, and can quickly trace and recall when there is a problem.
3. Information warning: Early warning of super-qualified production and operation of various enterprises; abnormal warning of the amount of drug sales, which can indicate whether there is drug abuse, or possible early warning of a certain drug for a short period of time; drug delivery and receipt Verify the warning of quantity and variety, and find out whether the drug is lost in time.
4. Terminal mobiles law enforcement. Drug regulatory and auditors can be easily audited at the right time through mobiles law enforcement systems, such as through the Internet or via mobiles phoness.
5. One code, breaking through the traditional one-class one-code mechanism, to uniquely identify and track each product, and realize the unified functions of government supervision, logistics application, merchant settlement, and consumer inquiry. Tracking everything through the entire process ensures that the product is monitored from the factory to the customer.
6. The centralized storage of dynamic information in the database is the limitation that the breakthrough quality information and the circulation dynamic information cannot be printed in advance. The supervision network stores the product dynamic information in a large-scale supervised database in real time, and simultaneously satisfies the real-time dynamics of production, circulation, consumption and supervision. Information sharing usage requirements.
7. National coverage Due to the characteristics of product production and national circulation sales, only the system network platform that achieves unified and seamless coverage throughout the country can meet the requirements of full-scale supervision.
8. Tracking the whole process of the closed source information collection of the production source and circulation consumption of the product, and possessing the technical functions of information sharing and process linkage of quality inspection, industry and commerce, commerce, drug supervision and other related departments, in order to realize the quality of the products. Traceability, accountability, problem recalls, and law enforcement counterfeiting provide the necessary information support.
9. Consumer inquiry can conveniently check the authenticity and quality information of drugs by means of SMS, telephones, network and terminal measures. The information available to consumers is: generic name, dosage form, specifications; production company, date of production, batch number, expiration date, etc. If problems are found, you can contact the local food and drug regulatory authorities.