Patients give staff in health and social care personal information about themselves all the time and they trust that we will protect the information they give. As we move to a more electronic age, where information can be shared more easily, and across many more types of organisations, there has been an urgent need to review 'information governence' and the balance between protecting patient information and its sharing to improve patient care. Information is collected in data bases which are used in a variety of ways for research. When I served on an NHS research ethics committee we were always concerned that information about patients in trials would be protected and that they should be able to give informed consent to the information being used. With publication today of the Caldicott Review, the Health Secretary Jeremy Hunt has said that 1)any patient who does not want personal data held in their GP record to be shared with the Health and Social Care Informati
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