Medical Devices – Latest Updates

European Commission Issues Language Requirements for Medical Device Manufacturers

23 January 2024

On 17th January 2024, the European Commission published the overview of language requirements for the product information and instructions to be provided with medical devices (MD) and in vitro diagnostic devices (IVD) in the European Union. The overview tables (MD and IVD) should help manufacturers better understand which information in which languages needs to be provided in a specific country.

Subscribe to our Medical Devices News

Stay up to date on regulatory issues relating to the approval and marketing of medical devices


WordPress Cookie Plugin by Real Cookie Banner