CATrialAuthorisation object

Regulatory and ethics bodies involved in approval process

Regional Ethics Committee

Regulatory and ethics bodies involved in approval process for trials including patients

Regional Ethics Committee
Medicines Agency in some cases additionally involved

Regulatory and ethics bodies involved in approval process for trials including including healthy participants

Regional Ethics Committee
Medicines Agency in some cases additionally involved

Regulatory and ethics bodies involved in approval process for trials including vulnerable population

Regional Ethics Committee

Registration requirements for clinical trials including patients

Registration mandatory

Registration requirements for clinical trials including healthy participants

Registration mandatory

Registration requirements for clinical trials including vulnerable population

Not applicable

CA - Submission required to

National CA
Institutional CA
International CA
International CA involved in some cases

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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