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China Aesthetic Syringe And Solid Connector Industry Status Quo
Dr.c | Updated: Oct 25, 2017


China Aesthetic Syringe And Solid Connector industry from small to large, rapid development, has now become a complete range of products, innovative ability to continuously increase the market demand is very strong sunrise industry. In particular, in recent years, Aesthetic Syringe And Solid Connector industry to further accelerate the pace of development, not only for many years to maintain double-digit growth in output value, and the number of products exported and technological content is also rising.
With the international industry to accelerate the transfer, China will become a global Aesthetic Syringe And Solid Connector an important production base, some of the original dependence on imported equipment and equipment is gradually achieved domestic alternative imports. At the same time, many domestic provinces and cities to Aesthetic Syringe And Solid Connector industry as a new economic growth point, pay close attention to nurturing. Experts pointed out that the next ten to fifteen years, China Aesthetic Syringe And Solid Connector industry will enter a high-speed development stage.
According to the latest data show that in 2009, the Pearl River Delta, the Yangtze River Delta and the Bohai Bay Industrial Cluster to lead the development of the industry, Guangdong, Jiangsu, Shanghai, Zhejiang, Fujian, Beijing, Shandong, Liaoning, Hubei and Tianjin provinces and cities before the column 10 exports, of which Guangdong Province exports amounted to 28.82, accounting for 23.54%, among the best.
At the same time, we must also see the domestic high-end medical equipment has been basically a multinational company's products firmly occupy, China Aesthetic Syringe And Solid Connector industry development is weak, Aesthetic Syringe And Solid Connector regulatory start late, Aesthetic Syringe And Solid Connector The phenomenon of small, multi-scattered and low-level competition has not yet been fundamentally changed, and it has become a matter of urgency to accelerate the technological innovation capability of Aesthetic Syringe And Solid Connector industry and strengthen the production, research and research of medical equipment research and development. How to avoid the vicious price war, play an inherent advantage, enhance the competitiveness of many manufacturers are thinking about the problem.
In order to maintain the seriousness of the registration of the Aesthetic Syringe And Solid Connector, maintain the authority of the Aesthetic Syringe And Solid Connector. The author believes that Aesthetic Syringe And Solid Connector is required to set up a new product registration category. I suggest that Aesthetic Syringe And Solid Connector to determine the type of new product registration should be carried out as follows:
First of all, all Aesthetic Syringe And Solid Connector new product registration category, whether it is the first category or the second category and even the third category of products, unified by the provincial food and drug regulatory authorities to review and determine the production enterprises to issue a corresponding proof , At the same time to the State Food and Drug Administration for the record.
Second, by the manufacturer according to the provincial regulatory authorities issued a certificate to the corresponding Aesthetic Syringe And Solid Connector regulatory authorities to declare Aesthetic Syringe And Solid Connector registration procedures. The provincial regulatory authorities that is the first category Aesthetic Syringe And Solid Connector, the enterprise to the corresponding municipal regulatory authorities to declare the registration; is the second category Aesthetic Syringe And Solid Connector, the enterprise to the provincial management department to declare registration; Three types of Aesthetic Syringe And Solid Connector, the enterprise to the State Food and Drug Administration to declare the registration.
Once again, if a Aesthetic Syringe And Solid Connector product is recognized by the provincial regulatory authorities as the third category, and the enterprise to the State Food and Drug Administration to declare, the National Bureau that the product for the second category or the first category of products, then By the national bureau issued by the corresponding proof, by the enterprise to prove to the corresponding regulatory authorities to declare the registration.
Finally, when the National Bureau examines the filing materials of the provincial regulatory authorities, if the management category identified by the provincial regulatory authorities is considered to be incorrect, it can be adjusted in the corresponding classification of the document, but the previously registered product is still valid until When the product is re-registered, the manufacturer will then adjust it according to the new management category stipulated by the National Bureau.

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