Presentations from the webinar on clinical investigations of medical devices have been published on Fimea's website

On 17 May 2022, the research webinar organised by Fimea discussed the changes brought about by the new EU legislation to the application and notification processes, application documents and assessment of clinical investigations of medical devices and in vitro diagnostic medical devices. Other topics included the requirements laid down in national legislation and Fimea's regulations for clinical investigations and performance studies conducted in Finland.

The webinar presentations as well as the questions presented on the chat forum during the webinar and their answers have now been published on Fimea's website.

Medical devices webinars (in Finnish)