Analysis information management system

Abstract

In this analysis information management system, when a user has performed a predetermined operation on a client terminal, a display unit displays a data manager screen (100). A data file list (102) inthe screen (100) displays files that are among the analysis data files registered in a database, and that satisfy refinement criteria. When the user has requested a selection of "Creation of Report Set" (105) in an operation menu (104) after selecting a plurality of files for which the user desires to create a final result record, the selected plurality of analysis data files, and analysis reportfiles and audit trail report files associated with these data files, are read from the database and transmitted to the client terminal. The client terminal then creates a data list including the names of analysis data files, etc., creates a final result record report by aggregating the data list, the description in the audit trail reports, and the description in the analysis reports, etc. together, converts the created final result record report into a PDF file, and registers the PDF file in the database.

Description

technical field [0001] The present invention relates to a method for storing and storing data collected by various analytical devices such as a chromatograph, a mass spectrometer, and a spectrophotometer, and processing results such as calculated values ​​obtained by analyzing and processing the data. Managed analytics information management system. Background technique [0002] In recent years, in the processing and management of various data obtained by analysis equipment such as gas chromatograph (GC), liquid chromatograph (LC), mass spectrometer, etc., in almost all cases, a computer equipped with dedicated software is used. computer. In particular, recently, a plurality of analysis devices, computers such as client terminals, database servers, etc. A large-scale system interconnected by network lines (see Non-Patent Document 1, etc.). In general, in such an analysis information management system, processing results such as data obtained for a sample in an analysis de...

AI Technical Summary

Problems solved by technology

[0006] However, the work of creating such a final result record is very troublesome and time-consuming

In addition, in order to ensure the integrity of data required by various restrictions related to electronic records / electronic signatures in "FDA 21CFR Part 11" of the U.S. Food and Drug Administration (FDA), it is necessary to select and analyze results Audit trails and analysis reports of the log information corresponding to the list and confirm that they correspond appropriately, but when the number of samples included in one group increases, the amount of lists and audit trails also becomes huge, so select the job and Confirmation operations are very time-consuming and easily lead to operational errors

In addition, in the past, when it is necessary to obtain the final result record, it is necessary to perform the work of collecting the required information as described above, so it is difficult to recreate the final result record that has been created, and it is also difficult to ensure the recreated final result record. Identicality with previous end result records

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