ECGeneralEthicalReview object

Submission for Ethical review mandatory for

All clinical investigations of MD
(falling within the scope of the Medical Devices Directive)

Regulatory and ethics bodies involved in approval process

Competent Authority/-ies (CA)
Ethics committee(s)

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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