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Information to help you understand the difference between individual care and research and planning purposes, when you are using or disclosing data.

The national data opt-out does not cover data disclosures that you're required to make by law.

Patient data must be looked after carefully in line with the law. This guidance covers data protection legislation and other protections for patient data.

Leaflets, posters, recommended text for privacy notices and more information you can use, to help your patients understand their national data opt-out choice.

Guidance and information for health and care staff about the national data opt-out, including GP practice, nursing, midwifery, care, voluntary and helpline staff.

Streamline your research planning – locate and determine numbers of potential participants.

We offer safe, secure access to patient data and provide one-to-one support to help your trial run smoothly and efficiently. Our services can support you at every stage of the clinical trial process.

Find out how we invite people to take part in the Heartburn Health programme and how to opt out if you do not wish to receive a SMS text invite from NHS England.

The Heartburn Health programme aims to help improve care for people with heartburn, acid reflux and indigestion.