CASubmissionOfApplication object

Responsible for study submission

Sponsor

Guidance on submission of application

Regulatory guidance is available on the NoMA website in section:
legemiddelverket.no > English > Medical devices > Regulatory information
regarding medical devices

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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