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Design And Implementation Of Pharmaceutical Factory Quality Inspection Information Management System

Posted on:2014-01-13Degree:MasterType:Thesis
Country:ChinaCandidate:C F YangFull Text:PDF
GTID:2248330398960630Subject:Software engineering
Abstract/Summary:PDF Full Text Request
Pharmaceutical factory quality inspection and information management system, which is under the jurisdiction of Quality Supervision, Inspection and pharmaceutical companies at various sub-sectors within the linked via LAN, constitute a whole, provide convenient, accurate and efficient service for product to be packaged as raw materials in the pharmaceutical production process, packaging materials and semi-finished products, finished product quality inspection, in order to ensure quality standards in the pharmaceutical manufacturing process, to avoid the problems and drawbacks of manual. The system is mainly used to the product to be packaged according to the defined inspection of the internal standard, a variety of raw materials, auxiliary materials, semi-finished, finished, return the product to the relevant inspection or LAN data inspection, and enter the back-end database. In this way, each time you enter the result can be automatically generated report, ledger, reports, etc., provide a reliable basis for other departments and the department’s late work and protection.The system is in the depth of a pharmaceutical company to conduct a detailed needs analysis, access to the research status at home and abroad, and implemented after careful argument. According to the present and future of enterprise integration needs, the system uses the C/S structure, front development tools PowerBuilder9.0. the background using SQL Server2000as a server. The papers describe the focus of various product coding principles, classification structure and report style, and report scientific coding design and reasonable design.Design and Implementation of a system based on pharmaceutical quality control system, including inspection standards (testing of raw materials, packaging materials testing, product testing, research products), inspection report (intermediate products, bulk products, finished products, returns), test the ledger (finished ledger, semi-finished products Ledger Returns Ledger, Liuyang ledger), inspection reports (intermediate products and finished products, raw materials, packaging inaterials)system maintenance (all kinds coding maintenance staff privileges maintenance, backup and recovery) five modules. The system solves the complicated operation of the old system, input trouble, difficult to maintain, on user requirements, high error rate, a long cycle of the system feedback defects, to solve the problem of large amounts of data in the work processing, thereby reducing the work load and save a lot of manpower and material resources, and improve work efficiency, modern science and business management.
Keywords/Search Tags:Pharmaceutical Companies, Information Management, Drug Supervision, Quality Inspection, C/S
PDF Full Text Request
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