CATrialAuthorisation object

Regulatory and ethics bodies involved in approval process

Competent Authority/-ies (CA)
National Ethics Committee
NHS R&D (Research & Development) Forum

CA - Submission for authorisation mandatory for

All clinical trials on Medicinal Products (MP)

CA - Submission required to

National CA

Additional Information

Use the MHRA’s online algorithm "Is it a clinical trial of a medicinal product?" to find out if your study needs MHRA authorization, available on the MHRA's website.

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