Dahuanong (the emerging area of the pharmaceutical company) successfully passed the veterinary drug GMP acceptance

2020-10-21

Recently, the Guangdong Provincial Department of Agriculture and Rural Affairs veterinary drug GMP working Committee office appointed veterinary drug GMP inspection team, Dahuanong pharmaceutical company (emerging area) 11 production lines (reinspection) for a period of two days of veterinary drug GMP inspection and acceptance work.

 Inspection team through the briefing, on-site inspection, file review, answer questions into the GMP operation, in the process of inspection into production workshop, quality inspection area and dangerous goods library related facilities and carried out a comprehensive, serious and meticulous on-site inspection, at the same time according to the veterinary drug GMP criteria refer to Dahuanong GMP system files and operation records. Through the on-site inspection and acceptance of the company's personnel equipment, plant facilities and equipment, process flow, material management, health management, quality management and other hardware and software, we can understand the specific situation of the production line, production workshop, production link, product quality and safety production control measures in detail. The inspection team unanimously assessed that Dahuanong 11 vaccine production lines are qualified production lines in compliance with the veterinary GMP standards.



Finally, Chen Ruiai, Vice President of the Group and President of Dahuanong Division, expressed his sincere thanks to the valuable opinions and suggestions of the veterinary drug GMP acceptance experts. At the same time, he congratulated and thanked the company for passing the field acceptance of the veterinary drug GMP. Combined with the guidance of the expert group, he proposed the work requirements for the next step of the new version of the GMP. Taking the implementation of the new version of veterinary drug GMP as an opportunity, I am good at learning the new version of veterinary drug GMP new regulations, new technologies, new standards, supporting high standard hardware facilities, strengthen the internal GMP process management, and do the work specialized and fine.



Writing / photo, Ou Xilan, Jian Zhiqiong

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