CASubmissionOfApplication object

Responsible for study submission

Sponsor
Legal representative domiciled in the EU/EEA

Guidance on submission of application

Detailed guidance on the Notification procedure for non-CE- marked (pre market) MD to the CA as well as for CE-marked MD (post market) is available on the Ministry of Health’s website.

This project (ECRIN Integrating Activity/ECRIN-IA) has received funding from the European Union’s Seventh Framework Programme for research, technological development and demonstration under grant agreement no 284395
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