ECGeneralEthicalReview object

Submission for Ethical review mandatory for

All clinical trials on Medicinal Products (MP)

Submission to CA and EC to be performed in the following order

In parallel

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
Feedback