藥品電子監(jiān)管碼

作為國(guó)內(nèi)外智能自動(dòng)化設(shè)備研發(fā)企業(yè),上海陸甲自動(dòng)化科技有限公司的技術(shù)服務(wù)為中國(guó)制造業(yè)提供了與國(guó)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(yīng)用于:制藥、食品、飲料、日化、保健品、電子、電器、化工、汽車(chē)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(duì)藥品在生產(chǎn)及流通過(guò)程中的狀態(tài)監(jiān)管，實(shí)現(xiàn)監(jiān)管部門(mén)及生產(chǎn)企業(yè)產(chǎn)品追溯和管理，維護(hù)藥品生產(chǎn)商及消費(fèi)者的合法權(quán)益。依靠覆蓋藥監(jiān)網(wǎng)平臺(tái)完成產(chǎn)品狀態(tài)查詢(xún)、追溯和管理功能。

1. 從生產(chǎn)出廠、流通、運(yùn)輸、儲(chǔ)存直至配送給醫(yī)療機(jī)構(gòu)的全過(guò)程在藥品監(jiān)管部門(mén)的監(jiān)控之下。

2. 實(shí)時(shí)查詢(xún)每一盒、每一箱、每一批重點(diǎn)藥品生產(chǎn)、經(jīng)營(yíng)、庫(kù)存以及流向情況，遇有問(wèn)題時(shí)可以迅速追溯和召回。

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

4. 終端移動(dòng)。藥品監(jiān)管和稽查人員可以通過(guò)移動(dòng)系統(tǒng)，如通過(guò)上網(wǎng)，或通過(guò)手機(jī)便利地在現(xiàn)場(chǎng)適時(shí)稽查。

5. 一件一碼,突破了傳統(tǒng)一類(lèi)一碼的機(jī)制，做到對(duì)每件產(chǎn)品唯①識(shí)別、全程跟蹤，實(shí)現(xiàn)了政府監(jiān)管、物流應(yīng)用、商家結(jié)算、消費(fèi)者查詢(xún)的功能統(tǒng)一。對(duì)每一件物品全程追蹤，可以確保產(chǎn)品從出廠到客戶(hù)使用全程監(jiān)控。

6. 數(shù)據(jù)庫(kù)集中存儲(chǔ)動(dòng)態(tài)信息為突破質(zhì)量信息和流通動(dòng)態(tài)信息無(wú)法事先印刷的局限，監(jiān)管網(wǎng)對(duì)產(chǎn)品動(dòng)態(tài)信息實(shí)時(shí)集中存儲(chǔ)在超大規(guī)模監(jiān)管數(shù)據(jù)庫(kù)中，同時(shí)滿足了生產(chǎn)、流通、消費(fèi)、監(jiān)管的實(shí)時(shí)動(dòng)態(tài)信息共享使用需求。

7. 全國(guó)覆蓋由于產(chǎn)品一地生產(chǎn)、全國(guó)流通銷(xiāo)售的特點(diǎn)，只有做到全國(guó)統(tǒng)一、無(wú)縫覆蓋的系統(tǒng)網(wǎng)絡(luò)平臺(tái)才能滿足全程監(jiān)管的要求。

8. 全程跟蹤監(jiān)管網(wǎng)對(duì)產(chǎn)品的生產(chǎn)源頭、流通消費(fèi)的全程閉環(huán)信息采集，具備了質(zhì)檢、工商、商務(wù)、藥監(jiān)等各相關(guān)部門(mén)信息共享和流程聯(lián)動(dòng)的技術(shù)功能，為實(shí)現(xiàn)對(duì)產(chǎn)品的質(zhì)量追溯、責(zé)任追究、問(wèn)題召回和打假提供了必要的信息支撐。

9. 消費(fèi)者查詢(xún)可以借助短信、電話、網(wǎng)絡(luò)以及終端舉措措施等形式利便的查詢(xún)藥品真實(shí)性和質(zhì)量信息。消費(fèi)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(hào)、有效期等，假如發(fā)現(xiàn)問(wèn)題，可以與當(dāng)?shù)氐氖称匪幤繁O(jiān)管部門(mén)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.