藥品電子監(jiān)管碼

藥品電子監(jiān)管碼

作為國內(nèi)外智能自動化設備研發(fā)企業(yè),上海陸甲自動化科技有限公司的技術(shù)服務為中國制造業(yè)提供了與國際同步的藥品電子監(jiān)管碼技術(shù)解決方案。條碼系統(tǒng)應用于:制藥、食品、飲料、日化、保健品、電子、電器、化工、汽車工業(yè)及塑料與五金等各大行業(yè)！

藥品電子監(jiān)管碼管理系統(tǒng)是針對藥品在生產(chǎn)及流通過程中的狀態(tài)監(jiān)管，實現(xiàn)監(jiān)管部門及生產(chǎn)企業(yè)產(chǎn)品追溯和管理，維護藥品生產(chǎn)商及消費者的合法權(quán)益。依靠覆蓋藥監(jiān)網(wǎng)平臺完成產(chǎn)品狀態(tài)查詢、追溯和管理功能。

1. 從生產(chǎn)出廠、流通、運輸、儲存直至配送給醫(yī)療機構(gòu)的全過程在藥品監(jiān)管部門的監(jiān)控之下。

2. 實時查詢每一盒、每一箱、每一批重點藥品生產(chǎn)、經(jīng)營、庫存以及流向情況，遇有問題時可以迅速追溯和召回。

3. 信息預警各企業(yè)超資質(zhì)生產(chǎn)和經(jīng)營的預警；藥品銷售數(shù)量異常預警，可以指示是否有藥物濫用，或可能某種藥物短時間大量售出提示可能的疾病流行預警；藥品發(fā)貨與收貨數(shù)量和品種核實預警，及時發(fā)現(xiàn)藥品是否流失。

4. 終端移動。藥品監(jiān)管和稽查人員可以通過移動系統(tǒng)，如通過上網(wǎng)，或通過手機便利地在現(xiàn)場適時稽查。

5. 一件一碼,突破了傳統(tǒng)一類一碼的機制，做到對每件產(chǎn)品唯①識別、全程跟蹤，實現(xiàn)了政府監(jiān)管、物流應用、商家結(jié)算、消費者查詢的功能統(tǒng)一。對每一件物品全程追蹤，可以確保產(chǎn)品從出廠到客戶使用全程監(jiān)控。

6. 數(shù)據(jù)庫集中存儲動態(tài)信息為突破質(zhì)量信息和流通動態(tài)信息無法事先印刷的局限，監(jiān)管網(wǎng)對產(chǎn)品動態(tài)信息實時集中存儲在超大規(guī)模監(jiān)管數(shù)據(jù)庫中，同時滿足了生產(chǎn)、流通、消費、監(jiān)管的實時動態(tài)信息共享使用需求。

7. 全國覆蓋由于產(chǎn)品一地生產(chǎn)、全國流通銷售的特點，只有做到全國統(tǒng)一、無縫覆蓋的系統(tǒng)網(wǎng)絡平臺才能滿足全程監(jiān)管的要求。

8. 全程跟蹤監(jiān)管網(wǎng)對產(chǎn)品的生產(chǎn)源頭、流通消費的全程閉環(huán)信息采集，具備了質(zhì)檢、工商、商務、藥監(jiān)等各相關(guān)部門信息共享和流程聯(lián)動的技術(shù)功能，為實現(xiàn)對產(chǎn)品的質(zhì)量追溯、責任追究、問題召回和打假提供了必要的信息支撐。

9. 消費者查詢可以借助短信、電話、網(wǎng)絡以及終端舉措措施等形式利便的查詢藥品真實性和質(zhì)量信息。消費者可以獲得的信息有：藥品通用名、劑型、規(guī)格；出產(chǎn)企業(yè)、出產(chǎn)日期、出產(chǎn)批號、有效期等，假如發(fā)現(xiàn)問題，可以與當?shù)氐氖称匪幤繁O(jiān)管部門聯(lián)系。

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 law enforcement. Drug regulatory and auditors can be easily audited at the right time through law enforcement systems, such as through the Internet or via phones.

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, telephone, 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.