U.S. FDA Latin America Office, IMDRF: WGs and Priorities, MD Division (CDRH) & LatAm Activities, FDA Standards & Conformity Program/Policy and MDSAP & ISO13485.
U.S. Food and Drug Administration
The Center for Devices and Radiological Health (CDRH) – FDA provides a web page for multimedia industry education. The modules available describe many aspects of medical device regulations covering both premarket and postmarket topics.
To know more about CDHR Learn, click here.
You may find CDHR Learn resources in Spanish here.