Purpose

The The NHS screening programmes develop develop and improve as new information becomes available. This information can include:

• new tests
• a better understanding of conditions we screen for
• new ways to engage people in screening decisions

Screening programmes provide a unique opportunity for researchers to explore new tests, treatments and specific hypotheses relating to the screening programmes from a population perspective.

Data collection is integral to all screening programmes and a wealth of data is available to inform policy-making and research.

NHS screening programmes are responsible for ensuring data collected nationally and locally is managed in accordance with with data protection and information governance requirements.

It is essential that research, evaluation and audit are feasible, of high quality and protectsprotect the safety of patients.

Any research activity must be undertaken in line with current legislation and guidance. Access to data sets comprising comprising identifiable or potentially identifiable screening data or or tests requires appropriate legal gateway assurances.

Approval from the NHS Health Research Authority (HRA)(HRA) Confidentiality Advisory Group (CAG)(CAG) is needed for some studies using identifiable data without consent. See See guidance for for CAG applicants applicants for for more information.

NHS screening programmes encourage well-designed research that addresses important new questions that will inform, guide and improve the programmes.

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Application Dataprocess

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