China Quality News Network News learned from the official website of the State Food and Drug Administration that in accordance with the Zhejiang Provincial Government's deepening of the construction of "four lists and one network" and the reform and deployment of the "delegation, regulation and service" approval system, the first batch of five "license online application, express delivery" "Da" approval items were officially launched on May 20, 2016, two of which are medical device registration items. By the end of the year, 617 items of "change of registration items of Class II medical devices" and 256 items of "medical device clinical trial management and filing" had been handled, accounting for 45% of all medical device registration items of the bureau during the same period.

The new "Internet +" approval mode of "online application for licenses and express delivery" facilitates applicants and greatly saves time and costs. In 2017, Zhejiang Food and Drug Administration will focus on promoting the construction of informatization and electronic file system in response to the problem that the original data of medical device registration application materials are too many and complex, and strive to review and approve medical devices such as renewal of registration, change of registration license items, and new registration. The matter is implemented step by step.