Workflow configuration implementation method and system based on laboratory information management system

Abstract

The invention provides a workflow configuration implementation method and system based on a laboratory information management system, and the method comprises the steps: reading existing flow information, and generating a to-be-configured inspection flow; determining a workflow node of each inspection process, and determining a workflow node needing to be configured; setting the operation authority of each workflow node, wherein the operation authority can control the operation of the workflow node; according to the inspection process, setting the sequence of workflow nodes to form an inspection workflow; performing permission configuration on the workflow; judging whether the workflow conforms to the SOP specification or not, and if so, taking effect on the workflow, and if not, invalidating the workflow. By utilizing the activity workflow, different inspection workflows are registered for different samples according to a general operation flow of a laboratory in the pharmaceutical industry, so that the samples can be inspected according to SOPs of the samples, the GMP specification is met, and code development work and related verification work are reduced.

Description

technical field [0001] The invention relates to the field of laboratory information management of pharmaceutical enterprises, in particular to a method and system for implementing workflow configuration based on a laboratory information management system. Background technique [0002] The application of domestic pharmaceutical enterprise laboratory information management system is currently in its infancy. The laboratories of most pharmaceutical companies still use manual methods to manage the laboratory, and complete manual inspection processes such as sample management, process records, and inspection result verification through paper records. With the increase in the number of samples tested, the scale of laboratory testing The expansion of the laboratory and the continuous improvement of the requirements of the laboratory, the traditional laboratory management methods can no longer meet the needs of the business. And with the implementation of the new GMP (Good Manufact...

AI Technical Summary

Problems solved by technology

[0004] At present, the inspection process of various samples in the pharmaceutical laboratory information management system is still in the stage of customized development, the software development cost is high, and the maintenance investment is large. How to avoid a large number of customized development of the inspection process requires the real realization of the software of the pharmaceutical laboratory information management system. Productization, further reducing software verification costs for pharmaceutical companies

Images