We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » China May Streamline Regulations for Device Registration, Trials
China May Streamline Regulations for Device Registration, Trials
November 13, 2009
China’s State Food and Drug Administration (SFDA) soon will no longer require devicemakers to register products in the country of export as a condition
of registration and will not automatically require clinical trials in China for certain classes of devices.
To View This Article:
Login
Subscribe To International Medical Device Regulatory Monitor