The national data opt-out gives everyone the ability to stop health and social care organisations from sharing their confidential patient information for research and planning purposes.
This opt-out applies to the use of data for purposes beyond your individual care, such as research into new treatments, planning health services, or analysing population health trends.
Important: From July 2022, it is a legal requirement for all health and social care CQC registered organisations to be compliant with the national data opt-out.