The informatization project of pharmaceutical company is included in the key list of "integration of the two".
Release time:
2020-08-14
pharmaceutical company is listed in the key list of "integration of two modernizations"
this newspaper recently learned from the competent department that the "ERP/MES full-process informatization" project of peak pharmaceutical company is listed in the key list of "integration of two modernizations" in Jinhua city and has now entered the publicity period.
In order to speed up the in-depth integration of informatization and industrialization, according to the evaluation criteria in Jinhua City's "Several Opinions on Accelerating Informatization Construction" and "Jinhua City's Measures for the Management of Key Projects for Integration of Informatization and Industrialization", 148 projects were listed as the key projects of Jinhua City's "Integration of Industrialization and Industrialization" in 2017 . Jianfeng Pharmaceutical's "ERP/MES Full Process Informatization" project was finally included in the list after being recommended by Jinhua Economic and Information Committee, material review and expert review. The subsystems at the level of
of ERP/MES full-process informatization project include sales system, procurement system, MRP system, GMP QbD system, connecting UFIDA financial software and HR system. The subsystems at the level of MES include industrial data acquisition and monitoring system, GAMP/MES system, eBPR( electronic batch production record system ) , cGMP quality assurance system, QC/eBTR (QC process and electronic batch inspection record system ) , LIMS system, etc, after the completion of the construction, the visualization of drug production process and the collection and integration of industrial data will be realized. Realize the electronization of drug production process parameters, electronic batch production and inspection records; The realization of industrial data information integration and big data will also conform to the regulatory concept of drug production GMP data integrity and quality traceability to the greatest extent. The establishment of a unified enterprise information platform will eliminate information islands and realize data integration, which will help ensure the quality of drugs, greatly improve work efficiency, reduce business risks, and provide assistance to the internationalization of peak pharmaceutical products. (Song Shijie)
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