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  • Categories:关于我们
  • Time of issue:2019-05-11 00:00:00
  • Views:56
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Our company passed the GMP certification for the first time in 2004. Therefore, our company has initially established and improved the quality management system since 2004, equipped with the necessary drug quality management personnel, established and updated various management software that meets the characteristics of our company, and verified and tested. Operation, comprehensively improve our company's pharmaceutical production and quality management support capabilities.

[Hardware] According to the new GMP requirements, our company carries out the renovation and inspection of the plant, equipment and facilities. And in accordance with the new requirements, to ensure that the layout of the plant, equipment, facilities is reasonable, in line with the product process, the production system facilities can maximize the avoidance of pollution and cross-contamination on the basis of ensuring maximum capacity. Process water, air cleanliness level can meet product process requirements.

[Software] Continuously improve the quality management system to ensure that the qualifications of each position meet the requirements of the new edition, and the key positions are relatively stable. At the same time, the entire product production process is in a state of monitoring, and the GMP documents of each department are operable. The plant facilities, air purification system, purified water system, equipment and process are verified step by step according to the verification plan. At the end of the verification, the trial operation will be carried out to ensure that the new software can meet and adapt to the requirements of the production process of our company's products.

[Training] Develop a practical training plan and implement it step by step. Train the production, quality, material control, and technical departments by participating in the GMP training meeting organized by the provincial and municipal bureaus and by sending in and out. It is stipulated that each position should be trained and tested according to the post SOP, and the self-inspection work should be done regularly.

Our company has established a complete quality management system. The Quality Management Department is responsible for quality management and inspection. It has set up a raw material inspection room, a fragrance inspection room, a fragrance inspection room, a chromatographic detection room, a microbiology testing room, and a heavy metal testing room. A large number of advanced testing equipment such as liquid chromatograph, gas chromatograph, ultraviolet visible spectrophotometer, infrared spectrophotometer, moisture analyzer, PH meter, melting point analyzer, etc., there are 10 full-time inspectors. From the raw materials entering the factory to the product delivery layer to ensure the stability and continuous improvement of product quality.

Our company has always adhered to the "quality first, customer first" business philosophy, the long-term development of the company's various businesses, improve the company's economic and social benefits; "all members participate in development, refined quality and survival. Value-added service passengers Satisfaction, the whole process of excellence is the quality policy, to ensure the quality of the company's products, to provide better services to customers.

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2002

+

Establish

10000

Area

30

%

+

Technology

2000

+

Class I Purification Workshop

Foshan Nanhai Zhongnan Pharmaceutical Factory

Address: Xiahengtian Industrial Zone, Nanhai District, Foshan City, Guangdong Province

Zip code: 528244
Tel: 0757-85663377 0757-85609331
Fax: 0757-85602277
Mailbox:
znpharma@znpharma.com;becky@znpharma.com

佛山市南海中南药化厂

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