China FDA Releases Guidance on Acceptance of Foreign Medical Device Study Data

Published date22 January 2018
Law FirmRopes & Gray LLP
AuthorKatherine Wang
Subject MatterMedical Devices,China,Manufacturers,Clinical Trials,Regulatory Standards,China FDA

To continue reading

Request your trial

VLEX uses login cookies to provide you with a better browsing experience. If you click on 'Accept' or continue browsing this site we consider that you accept our cookie policy. ACCEPT