Hi all,
I would appreciate some help regarding mandatory translation to official languages in IVD and Medical Devices with the new Regulations.
1) Does anyone have an updated document with the language requirement in each country?
2) Do you think that a profesional-use standalone software interface would need to be translated into different languages?
Thank you in advance!
I would appreciate some help regarding mandatory translation to official languages in IVD and Medical Devices with the new Regulations.
1) Does anyone have an updated document with the language requirement in each country?
2) Do you think that a profesional-use standalone software interface would need to be translated into different languages?
Thank you in advance!