Countries within Europe have specific European translation requirements for computer software, Instructions for Use (IFU), packaging, and other Medical Device and Pharmaceutical labeling. In this ever-changing regulatory and international market clearance environment, it is vitally important for you to have this information at your fingertips. Without it you are unable to proactively properly plan your international market clearance strategy.
In addition to the language requirements there are trends and country-specific requirements for the medical device directives and pharmaceutical regulations.
With this comprehensive, easy-to-understand guide you will understand the necessary European Language requirements for both Medical Devices and Pharmaceuticals.