This rolling plan contains the list of essential implementing acts and actions for the transitional period as well as information on expected timelines and state-of-play.
Its 2 main sections are implementing acts and other actions/initiatives. The rolling plan will be reviewed quarterly to provide operators with the latest information.
The rolling plan can be used together with the ‘MDR/IVDR roadmap‘, jointly produced by the competent authorities for medical devices project (CAMD) and the European Commission.
The roadmap is more comprehensive. It gives an overview of all the expected initiatives (including guidance) during the transitional period.