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MINSHENG MEDICINE

Shaoxing Minsheng Pharmaceutical Co., Ltd.   Powered by www.300.cn 浙ICP备18055214号

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Quality system

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The Quality Assurance Department of Shaoxing Minsheng Pharmaceutical Co., Ltd. was established in 2003 and is directly under the leadership of the general manager of the company. It is responsible for all work related to quality management of the company. The two functional departments of the quality assurance department: QA of Quality Assurance Department and QC of Quality Assurance Department respectively perform the functions of quality supervision, management and quality inspection.
QA of Quality Assurance Department is responsible for establishing and improving the company's quality supervision system, and monitoring the whole process of material procurement, finished product release and sales. The company's entire quality system is managed through on-site inspections, periodic inspections, and regular quality reports, and GMP training is regularly organized.
Quality Assurance Department QC is responsible for the inspection of raw materials, finished products, intermediates, process water used in the company's production and environmental conditions. Since its establishment, the Quality Assurance Department has been strictly controlling from raw material procurement and production processes to finished product storage and sales release. All processes are operated in full compliance with GMP regulations. With GMP standards and FDA certification as the entry point, we adhere to the principle of “time sense, high starting point, high standard”, and fully integrate with the international community. Sophisticated quality inspection equipment and well-trained inspectors provide a reliable guarantee for product quality control. Product quality standards meet USP, BP, EP, JP and CP requirements.MINSHENG