Search results
The National Data Opt-Out (NDOO) service lets people decide whether their confidential patient information can be used for research and planning.
The Electronic Prescription Service (EPS) is for prescribers and dispensers and is used in primary, secondary and community care.
A terminology solution to help healthcare IT systems speak the same language, and make mapping codes between organisations faster and easier.
The National Care Records Service (NCRS) provides a quick, secure way for health and care workers to access national patient information to improve clinical decision making and healthcare outcomes and it is free to use.
Message Exchange for Social Care and Health (MESH) provides the ability to share data directly between health and care organisations and is the nationally recognised mechanism for this method of data sharing.
Primary Care Registration Management (PCRM) is a back-end service that enables patients to register with a GP practice.
The Personal Demographics Service (PDS) is the national master database of all NHS patients in England, Wales and the Isle of Man - holding basic patient details such as name, address, date of birth, contact details, registered GP, nominated pharmacy and NHS number. PDS has a National Back Office for...
A national service for managing information about organisations across health and social care.
Cohorting as a Service securely identifies groups of people with shared characteristics from national health data.
Summary Care Record (SCR) is a national database that holds electronic records of important patient information such as current medication, allergies and details of any previous bad reactions to medicines, created from GP medical records. It can be seen and used by authorised staff involved in the patient's...