Tongxie Enterprise, leveraging its understanding of the pharmaceutical extraction industry processes and its professional self-control team, is committed to providing excellent services to customers through professional digital overall solutions!
Therefore, Tongxie Enterprise has developed the pharmaceutical production management system software (TX-IMS)
The pharmaceutical production management system software (TX-IMS) automates the entire pharmaceutical production process. Through the automatic control of units such as multi-functional extraction, dual-effect ethanol concentration blending, and utility system detection, and by integrating other automatic control systems in the workshop, such as the slag discharge system, into the overall control system through communication methods, combined with the characteristics of the pharmaceutical extraction process, each unit is controlled automatically according to the process requirements. At the same time, through batch judgment, the material transfer between control units is controlled to ensure the smooth operation of the production process.
It also has abnormal alarm and interlock functions, which can enhance production stability, thereby improving production management level and efficiency, ensuring product quality, and laying a technical foundation for improving the process quality control level of the company's drug product extraction production, showcasing the modernization of the enterprise, and facilitating the realization of the digital extraction workshop.
The pharmaceutical production management system software (TX-IMS) captures the characteristics of the entire production process in the workshop. The automatic control system meets the following six performance requirements:
| User Requirements (URS,completed by the client, with suppliercooperation,in the standardization phase) | Functional Description (FS, Specification Phase) |
Hardware testing (system and module testing, logic function testing,systemlinkage testing) (verification phase) | Overview of Automatic Control Systems (Specification Phase) |
Hardware Design Specification (HDS,SpecificationPhase) | Anomaly testing (verification phase) |
| Process piping and instrumentation diagram | Software Design Specification (SDS, SpecificationPhase) |
3Q documents and user manuals (including IQ,OQ, PQ) (Reporting phase) | Control System I/O / Module Configuration Table (Inputs & Outputs) |
| Control system network structure diagram | Change control documents |
| List of equipment, valves,and instruments | Risk analysis (RA,risk assessment and control) (standardization phase) |
Software development and design (configuration or programming phase) | Design Description |
Design Qualification (DQ)(Specification Phase) | Software development coding and related documentation (configuration orprogramming phase) |
1.Acceptance inspection and handover
2.Equipment installation
3.On-site training
4.Installation of accessory equipment
5.On-site debugging
6.Installation of automatic control system
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