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Method for realizing standard and flow production of drugs

An implementation method and streamlined technology, applied in the field of pharmaceutical production supervision, can solve problems such as counterfeiting, and achieve the effect of avoiding artificial changes and standardizing production

Inactive Publication Date: 2014-07-30
ZHANGZHOU PIEN TZE HUANG PHARM
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Due to the operability of subsequent processing and production, the phenomenon of counterfeiting still exists

Method used

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  • Method for realizing standard and flow production of drugs

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Embodiment Construction

[0018] The present invention will be further described below in conjunction with the accompanying drawings and embodiments.

[0019] Such as figure 1 As shown, the present embodiment provides a method for realizing the standardized production of pharmaceuticals, which is characterized in that it includes the following steps:

[0020] Step S01: Report the production volume of the approved and registered drug to the relevant department, and obtain the supervision code and traceability code of the drug;

[0021] Step S02: Convert the supervision code and traceability code into a production identification code, and store it in correspondence with the production volume;

[0022] Step S03: Use the identification code as the order number, and retrieve the production volume corresponding to the identification code to form a picking list;

[0023] Step S04: send the picking list to the warehouse for picking;

[0024] Step S05: Maintain the product batch number and production date be...

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Abstract

The invention relates to a method for realizing standard and flow production of drugs. According to the method, a supervision department and the production process are combined, standard and flow production of drugs is ensured through reporting and recording, identification code forming, material obtaining, delivery to storage and subsequent corresponding feedback, standard production is guaranteed, flow type operation is adopted in the whole process, and potential safety hazards caused by man-made changes are avoided.

Description

technical field [0001] The invention relates to the technical field of pharmaceutical production supervision, in particular to a method for realizing standardized flow-through production of pharmaceuticals. Background technique [0002] The production of drugs generally needs to be reported to the Food and Drug Administration. Without reporting, it will lead to the trading of counterfeit and inferior drugs in the market, which will not only endanger the health of patients, but also affect the operation of regular enterprises. Existing drug production is through written reports to relevant departments, and after approval, each enterprise carries out subsequent processing and production by itself. Due to the operability of subsequent processing and production, the phenomenon of counterfeiting still exists. Contents of the invention [0003] In view of this, the object of the present invention is to provide a method for realizing standardized production of pharmaceuticals,...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): G06Q10/06
Inventor 陈顺逸严建斌何敏章
Owner ZHANGZHOU PIEN TZE HUANG PHARM