Coordinate Registration Testing in Chinese Lab Authorized by NMPA and Communicate Throughout the Testing Process
When applying for class II and class III medical device registration in China, registration testing shall be conducted. Clinical trials or registration application can be carried out only after the products passed the registration testing.
The medical device testing institutions shall carry out relevant registration testing on the products in accordance with the product technical requirements.
GeBiao can coordinate registration testing in Chinese labs authorized by NMPA and communicate throughout the testing process for your medical device products