Off-site regulation method used for medicine circulation

Abstract

The invention discloses an off-site regulation method used for medicine circulation. The method includes: by application of the computer information processing technology and the internet technology, enterprise related information of medicine manufacturers is collected, and the collected information is transmitted and stored to a data server; in the logistics transport link of medicines, transport condition information of the medicines is collected in real time, and the information is transmitted and stored to the data server; medicine wholesale and retail mechanisms or medical mechanisms carry out data and video collection and storage on goods examination information of the medicines; a medicine supervisory organization carries out real-time tracking and early warning on the above information; the medicine supervisory organization establishes a corresponding medicine enterprise credit or credit standing platform; and general public users can carry out inquiry and complaint operation. The off-site regulation method used for the medicine circulation effectively solves the problems that medicine supervisors are shorthanded, and investigation and evidence collection are difficult, provides related information and rigorous evidences and bases for medicine tracking and plays an active role in ensuring medication safety of the general public masses.

Description

technical field [0001] The invention relates to the field of supervision methods, in particular to an off-site supervision method for drug circulation. Background technique [0002] Drugs are special commodities for people to prevent and treat diseases, and the quality of drugs is directly related to the health and life safety of the people. Since the establishment of the drug supervision and management department, it has insisted on focusing on rectification on the one hand and standardization on the other hand. Through several years of hard work, the drug market has gradually changed from the original disorderly operation to orderly operation. The safety and effectiveness are more and more guaranteed. However, there are still many deficiencies and weak links in the traditional law enforcement supervision, such as: huge supervision workload, serious shortage of staffing, unable to realize dynamic tracking of safety supervision of drug circulation links, pharmaceutical comp...

AI Technical Summary

Problems solved by technology

However, there are still many deficiencies and weak links in the traditional law enforcement supervision, such as: huge supervision workload, serious shortage of staffing, unable to realize dynamic tracking of safety supervision of drug circulation links, pharmaceutical company operating sites, drug storage environment, etc.; It is difficult for enterprises to carry out early warning; it is difficult to obtain evidence during daily on-site inspection or law enforcement; it is difficult to trace the drugs with problems in the circulation process, and it is impossible to realize the recall; each business adopts an independent business system, each working independently, and resources cannot be shared, making relevant supervision departments Unable to carry out comprehensive analysis and scientific regulation

[0003] At present, there are many means of drug quality supervision, but the method of on-site manual recording is mainly adopted, especially for the production environment and storage environment of drugs, which are manually recorded by special personnel and posts, which will inevitably lead to data errors and unfavorable phenomena such as artificial fraud. Occurs, making drug supervision results lack of timeliness and authenticity

Since it is impossible to dynamically track and record the on-site situation, it is impossible to give early warning to enterprises with real-time problems. Therefore, when on-site inspection and evidence collection, most enterprises prepare in advance, and most of them are manually recorded, which makes it difficult to obtain evidence in the daily law enforcement process, resulting in the inability to supervise in place. It is difficult to trace the cause of non-compliant or regulated drugs, and it is even impossible to recall them

Although some pharmaceutical companies have independent business collection, such as temperature and humidity monitoring system, video monitoring system, pharmacist attendance system, etc., the drug supervision agency needs to supervise each pharmaceutical company, which not only has a heavy workload, but also has low supervision efficiency. , the data is too scattered and independent, and the availability rate is low, so it is impossible to carry out comprehensive analysis and business integration

In addition, due to the traditional manual recording methods, some information cannot be made public, and the general public has questioned the safety and credibility of drug quality

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