Registration and application of domestic/foreign diagnostic reagents, supporting instruments and software;European CE certification consulting and agency, THE United States FDA certification consulting and agency;Brazil ANVISA...

Provide innovative medical device application services for domestic and foreign enterprises engaged in the development of innovative IVD products (reagents, instruments, software), covering innovation policy consultation,...

The process of confirming or verifying the safety and effectiveness of the medical device to be registered under normal conditions of use in a medical device clinical trial institution certified by NMPA. It is divided into medical devices (MD) ....

Provide quality management system consulting services for enterprises engaged in IVD product (reagents, instruments, software) production activities (including self-built, commissioned R&D, commissioned production) in China, and committed to....