Hi, I need to know, if there is any legal requirement to register the same indications for a medical device as approved in the country or origin.
In case yes, could you please make a reference as to the law/guidance and country where such a requirement exists?
I am especially interested, if such a "written requirement" would be available for the region of Latin America.
Your help and feed-back is much appreciated.
Thanks a lot in advance,
Chinquada
In case yes, could you please make a reference as to the law/guidance and country where such a requirement exists?
I am especially interested, if such a "written requirement" would be available for the region of Latin America.
Your help and feed-back is much appreciated.
Thanks a lot in advance,
Chinquada