Hello,
My company met some problem during recent medical device registration process. We applied and got our CE Mark in 2010 through an UK's authorized representative. Since the UK has left the European Union, and their government now only provide with electronic-edition FSC(Free Sales Certificate). However, the Argentina government only accepts the hard-copy version of FSC. Under this situation, what is my company's best approach to deal with this? Thank you so much!
My company met some problem during recent medical device registration process. We applied and got our CE Mark in 2010 through an UK's authorized representative. Since the UK has left the European Union, and their government now only provide with electronic-edition FSC(Free Sales Certificate). However, the Argentina government only accepts the hard-copy version of FSC. Under this situation, what is my company's best approach to deal with this? Thank you so much!