The european commission, in collaboration with member states, has recently released two essential documents outlining language requirements under the mdr (medical device regulation) and ivdr …This guide cuts through the complexity of ivdr language requirements, offering clear, actionable insights to help manufacturers ensure their translations meet the necessary standards for successful …For easy reference, in january 2024, the european commission directorate-general for health and food safety published a table of all european union country and their ivdr language requirements, …Due to the member states’ mandate to determine local language requirements, union-level legal publications (such as the mdr and the ivdr) do not specify which national languages are required.Regulation (eu) 2017/746 on in vitro diagnostic medical devices (ivdr) contains different legal provisions that allow member states to determine language requirements for manufacturers at …Regulation (eu) 2017/746 on in vitro diagnostic medical devices (ivdr) contains different legal provisions that allow member states to determine language requirements for manufacturers at …