I mean the method for getting the go ahead for selling your particular medical device (into both public and private sector) (post CE mark approval) into the various terratories of the European Market.
There are some different points of view to this in different countries.
I can help in you with Poland for example - for all class IIb and III products an additional registration is required.
Should you need to do it I can help.
This site uses cookies to help personalise content, tailor your experience and to keep you logged in if you register.
By continuing to use this site, you are consenting to the use of cookies.