欢迎您来到上海陆甲自动化科技有限公司

不干胶贴标机产品检测设备条码追溯系统自动化生产线

药品电子监管码

暂无图片

药品电子监管码厂家

药品电子监管码价格



药品电子监管码

 

作为国内外知名智能自动化设备研发企业,上海陆甲自动化科技有限公司的技术服务为中国制造业提供了与国际同步的药品电子监管码技术解决方案。条码系统应用于:制药、食品、饮料、日化、保健品、电子、电器、化工、汽车工业及塑料与五金等各大行业!

药品电子监管码管理系统是针对药品在生产及流通过程中的状态监管,实现监管部门及生产企业产品追溯和管理,维护药品生产商及消费者的合法权益。依靠覆盖药监网平台完成产品状态查询、追溯和管理功能。

1. 从生产出厂、流通、运输、储存直至配送给医疗机构的全过程在药品监管部门的监控之下。

2. 实时查询每一盒、每一箱、每一批重点药品生产、经营、库存以及流向情况,遇有问题时可以迅速追溯和召回。

3. 信息预警各企业超资质生产和经营的预警;药品销售数量异常预警,可以指示是否有药物滥用,或可能某种药物短时间大量售出提示可能的疾病流行预警;药品发货与收货数量和品种核实预警,及时发现药品是否流失。

4. 终端移动执法。药品监管和稽查人员可以通过移动执法系统,如通过上网,或通过手机便利地在现场适时稽查。

5. 一件一码,突破了传统一类一码的机制,做到对每件产品唯①识别、全程跟踪,实现了政府监管、物流应用、商家结算、消费者查询的功能统一。对每一件物品全程追踪,可以确保产品从出厂到客户使用全程监控。

6. 数据库集中存储动态信息为突破质量信息和流通动态信息无法事先印刷的局限,监管网对产品动态信息实时集中存储在超大规模监管数据库中,同时满足了生产、流通、消费、监管的实时动态信息共享使用需求。

7. 全国覆盖由于产品一地生产、全国流通销售的特点,只有做到全国统一、无缝覆盖的系统网络平台才能满足全程监管的要求。

8. 全程跟踪监管网对产品的生产源头、流通消费的全程闭环信息采集,具备了质检、工商、商务、药监等各相关部门信息共享和流程联动的技术功能,为实现对产品的质量追溯、责任追究、问题召回和执法打假提供了必要的信息支撑。

9. 消费者查询可以借助短信、电话、网络以及终端举措措施等形式利便的查询药品真实性和质量信息。消费者可以获得的信息有:药品通用名、剂型、规格;出产企业、出产日期、出产批号、有效期等,假如发现问题,可以与当地的食品药品监管部门联系。

 

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

 

 

 


询价

AFozMFbYfm7sXbO+bz09FWyxS+jX9h4vCEs9K75yubA3e9P1L8OsXA65HL2EhpA1IRLLeaqZqDQhH2N6wucOmU1w63k7v4+E82C5rvJ34fBXzQOWP37daQ==