In November 30, 2016, Yinfeng genes passed on-site audit of Market Authority in high-tech new zone only one time and acquired class Ⅲ business license of medical devices.

According to the laws and regulations, the application of class Ⅲ business license of medical devices should pass all examinations and verifications of Jinan’s Food and Drug Administration and high-tech new zone’s Market Authority, and the process of examinations and verifications is extremely strict. The comprehensive department of the company pays high attention to this work and prepares through the gathering of laws and regulations, the integration of personnel, the formation of system document, the installation of storehouse and the selection of dedicated application computer software. Finally, this work is highly recognized by on-site audit group and passes on-site acceptance test successfully.

This shows that the business scope of companies involves and covers medical equipment, in-vitro diagnostics manufacture and software, and this takes a vital role in the increasing of types of company business and the creativity of business mode.