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Pharmaceutical companies to participate in drug production site management GMP training

Release time:

2020-07-22

Pharmaceutical Company Participated in Drug Production Site Management GMP Training

News 9# September 26 -28 , Jianfeng Pharmaceutical Factory organized workshop management personnel and QA to participate in the "Analysis of Common Defects in Drug Production Site Management and Production System" training organized by Feitian Education Group in Hangzhou, learn about on-site management of pharmaceutical production, analysis of common defects in production systems, and requirements for equipment documentation and data integrity in production systems.

In the process of FDA certification, EU certification and China certification in the enterprise, more and more inspectors are paying attention to the GMP compliance inspection on the production site. This training mainly focuses on the link design of quality control in the whole process of drug production. The training takes some practical cases as the starting point to help enterprises improve drug quality, on-site management related to production process control, key control and defect analysis in the production process, and reduce the risks of confusion and errors in the drug production process. The main content of

training is the comparative analysis of similarities and differences between FDA , EU and China GMP , analysis of production process-related defects in official inspections and audits at home and abroad, key points and precautions of production site inspections, design points and practical analysis of batch production process control records based on different registration processes, management requirements of production equipment, management of production-related documents and records, and data integrity management requirements in the production system.

Through training, the trainees of Jianfeng Pharmaceutical Factory increased their knowledge of drug production site management, production system equipment and documents and data integrity requirements, broadened their horizons, inspired ideas to solve common defects in production systems, and deepened their understanding of GMP .

After the training, the trainees also discussed some problems in the production site management of the enterprise with the training teachers. (Wang Weijian)

More information

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