Ningbo guides the development of medical equipment enterprises

Ningbo guides the development of medical equipment enterprises The Ningbo Municipal Bureau deepens its service to enterprises and provides practical services for enterprises. Recently, the deputy director of the Bureau Chen Shiben led the relevant staff to form a research group and successively went to Ningbo Meishan Bonded Port Area, Haier Shi Bio-Pharmaceutical Co., Ltd., Ningbo Tianyi Medical Instrument Co., Ltd., Zhejiang Guangci Medical Instrument Co., Ltd., and Ningbo. Enterprises such as Behua Import & Export Trading Co., Ltd. launched home delivery policies and policies.

In the Ningbo Meishan Bonded Port Area, the research team listened carefully to Deputy Secretary Hu Kui’s deliberations on the status quo and plans for the construction of the medical device industry park. The deputy director Chen Shiben introduced the current situation of the medical device industry and the development of the industry, and proposed cross-regional The policy interpretation of the establishment of business sites, etc., proposed suggestions for the cultivation and development of the medical device industry in the park, and expressed its willingness to actively provide support and assistance for the construction of the industrial park.

In Haiershi Biopharmaceutical Co., Ltd., Zhejiang Guangci Medical Instrument Co., Ltd., and Ningbo Tianyi Medical Devices Co., Ltd., Chen Shiben, deputy director of the company, and the person in charge of the company's plans for launching, major science and technology, and disease diagnostic reagent R&D projects and operations. Difficulties encountered were discussed and communicated, on-site interpretation of medical device industry policies and regulations, and in-depth inspections of production conditions. The company also cared about the medical equipment production and business conditions and procedures, product registration review standards, and application procedures. . On the issue of how to standardize development, several requirements are put forward for companies: First, we must strengthen the study of medical device laws and regulations and firmly establish the concept of safe production; Second, we must strengthen the construction of internal quality system and improve the quality of internal review; To cooperate with the regulatory authorities to carry out daily inspections, and gradually promote standardized production; Fourth, more than regulatory agencies to communicate, avoid detours, improve efficiency.

In the next step, the Ningbo Municipal Bureau will continue to monitor and supervise services, promote the standard development of enterprises, deepen the activities of service companies, and guide the healthy and rapid development of medical device companies in the city.

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