Informed Consent

The aim of this one-day workshop is to provide delegates with a practical overview of the process and requirements for seeking informed consent to undertake research in the NHS.

During the day we will have the opportunity to examine:

The final session of the day allows discussion of how informed consent should be managed in more complex situations, including research involving children and those who lack capacity to give informed consent. We will also explore the various situations where nurses may be receiving consent for genetic, epidemiological, translational research studies and clinical trials.

Course Facilitators: Dr Leslie Gelling and Kelly Gleason

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