CATrialAuthorisation object

Regulatory and ethics bodies involved in approval process

Ministry of Health/ Competent Authority
National Ethics Committee

CA - Submission for authorisation mandatory for

All clinical trials on Medicinal Products (MP)

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

In parallel

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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