To help startups and SMEs carry out their regulatory, quality and clinical research procedures, the French government is setting up a "Medical Device" Regulatory Diagnosis. It is financed as part of France 2030, jointly by the "Santé numérique" acceleration strategy and the Plan DM. It has an overall budget of €20m.

The "guichet" puts a project developer in touch with a referenced external expert specialized in procedures for setting up a quality system, compiling technical documentation and/or designing and writing clinical or medico-economic investigation protocols.

This window is aimed at innovative startups and SMEs developing medical devices and/or in vitro diagnostic medical devices. Over a period of 12 to 18 months, half the cost of the service will be covered.

This service is designed for startups and innovative SMEs developing medical devices and/or in vitro diagnostic medical devices.