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ZHEJIANG HISUN PHARMACEUTICAL CO.,LTD.
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Praziquantel has sufficient capacity for stable supply, CEP certificate has been obtained, JP site registration has been approved, both US DMF and VMF have been approved, and it has passed MOA review. As a comprehensive pharmaceutical enterprise with complete research, production and marketing value chain and multi-region development, Hisun Pharmaceutical owns three major production bases of APIs, with perfect production lines covering nearly 100 varieties, and is one of the important producers of speciality APIs in the world.
Hisun Pharmaceutical is equipped with advanced production equipment and facilities and testing instruments, and its production, testing and release follow the requirements of GMP; Hisun Pharmaceutical has a central research institute at its headquarters in Taizhou, a nationally-recognised enterprise technology centre, a provincial academician's workstation, and the first postdoctoral scientific research station in the province with independent enrolment qualification; the R&D platform is equipped with a R&D laboratory and a small and medium-sized pilot plant, which provides seamless linkage between the development and industrialisation of new products and new processes. The R&D platform is equipped with R&D laboratories and small and medium-sized pilot production workshops, providing a seamless connection from new product and process development to industrialisation.
Hisun Pharmaceutical is equipped with a professional quality management team and a perfect quality management system, covering the whole life cycle of drug quality;
The pharmaceutical administration system of Hisun Pharmaceutical can efficiently support the global registration affairs of customers and provide better products and services for global customers;
Hisun Pharmaceutical establishes an EHS laboratory, equipped with a professional research team and advanced experimental equipment, a perfect EHS integrated management system and a professional EHS management team to escort the company's safe production and green development. The laboratory management system passed CNAS certification in 2018. |
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Pharma Sources Insight June 2024: Globalization on the Go
