The national data opt-out allows a patient to choose if they do not want their confidential patient information to be used for purposes beyond their individual care and treatment - for research and planning.
Patients, or people acting for them by proxy, have control over setting or changing their own opt-out choice, and can change their mind at any time. In most cases health and care staff won't be involved - but it's helpful to understand how the process works so you can tell patients where to find out more about their choices.
If you do not want your personal data used for Planning and Research purposes please see further information here: National data opt-out
National guidance is available for:
Related documents
Page last reviewed: 25 April 2024
Next review due: 25 October 2024
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