Obtaining Informed Consent for Clinical Trials

This document describes the procedure for obtaining and documenting informed consent for Clinical Trials of Investigational Medicinal Products (CTIMPs).

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Obtaining Informed Consent for Clinical Trials

This SOP describes the procedure for obtaining and documenting informed consent for Clinical Trials of Investigational Medicinal Products (CTIMPs). This SOP applies to all clinical trials sponsored, co-sponsored or managed by King’s Health Partners (KHP) organisations.

Investigators should also follow the local consent policy of the NHS organisation where the trial is taking place.

Standard Operating Procedure: Obtaining Informed Consent

Obtaining Informed Consent SOP

Useful links

Informing participants and seeking consent: HRA guidance

Consent and participation information guidance: HRA