EU rules for medical devices and in vitro diagnostics - public consultation

The European Commission is preparing a public consultation document for Q3 2024. This initiative aims to help the Commission assess whether the new rules for medical devices and in vitro diagnostics are efficient, effective and proportionate, whether they meet current needs and whether they have added value.

Background information can be found here: EU rules on medical devices and in vitro diagnostics – targeted evaluation (europa.eu)