National Health Service data held in the Health Data Research Service will be subject to the National Data Opt-out, in line with national opt-out policy, and the right to object to data being processed under the UK General Data Protection Regulation.

National Health Service data held in the Health Data Research Service will be subject to the National Data Opt-out, in line with national opt-out policy, and the right to object to data being processed under the UK General Data Protection Regulation.

The Health Data Research Service (HDRS) will build on existing health research services, including the national and regional secure data environments, OpenSAFELY and NHS DigiTrials, which already support the safe, secure, and beneficial use of health data for research. As the model for delivery of HDRS is developed, we will consider how patients can exercise their choice as to how their data is used for research. Patients will continue to be able to exercise the National Data Opt-out.

The National Data Opt-Out was introduced in 2018, allowing patients, in specified circumstances, to opt-out of their confidential patient information being used for research or planning purposes. It has been mandatory since 31 July 2022.

The Health Data Research Service (HDRS) will deliver a single point of access to health data from multiple sources which will bring new treatments and cures to patients by safely enabling the use of patient data to super-charge research.

Over the past year a Department led team, with support from the Office for Life Science and NHS England colleagues, has been working to set up the service.

HDRS is being established as a Government Company, and Dr Melanie Ivarsson has been appointed as Chief Executive Officer and Baroness Nicola Blackwood as Chair. Work is now underway to incorporate and develop the service to ensure it is up and running as quickly as possible to deliver benefits for patients and researchers.

We are committed to the service being operational by December 2026, with new capabilities being progressively rolled out.

To ensure an appropriate commercial model is developed for the Health Data Research Service (HDRS), discovery work has been undertaken to gain insight into existing commercial models that might be applicable for the HDRS. This discovery work included engagement with 19 commercial organisations representing users of health data, allowing the development of a robust, up to date, and United Kingdom-wide evidence base. Decisions regarding what commercial model and pricing arrangement is used will be within the remit of the incoming HDRS senior leadership team.

I refer the Hon. Member to the answer I gave to the Hon. Member for Sleaford and North Hykeham on 30 October 2025 to Questions 78409 and 78410.

Keeping data safe and secure and ensuring patient and public privacy remain key principles of the Health Data Research Service (HDRS). The public will retain a right to opt out of specific uses of their data beyond their direct care, and these opt-outs will be respected with the implementation of HDRS.

Genomics England, Our Future Health and UK Biobank contribute important human data to the UK’s diverse research portfolio that supports alternative method development, including organ-on-a-chip, cell-based assays, functional genomics and computer modelling. The Health Data Research Service will also contribute in future, However, this research is not categorised by application, so calculating funding for alternative methods specifically is not possible. UKRI also invests £10 million annually in the National Centre for the Replacement, Refinement and Reduction of Animals in Research (NC3Rs), with future investment under review.

The Government will publish a strategy to support alternative methods later this year.

On 7 April 2025 the Prime Minister announced that the Government and the Wellcome Trust will invest up to £600 million to create a new Health Data Research Service, co-designed through engagement with the public and patients, data users, and stakeholder organisations.

Providing access to data for direct care purposes is not one of the Health Data Research Service’s planned capabilities. The Health Data Research Service will deliver a single point of access to health data for research from multiple sources, National Health Service and non-NHS. This service will bring new treatments and cures to patients by safely enabling the use of patient data to super-charge research, attracting investment and making the United Kingdom one of the best places in the world to conduct ground-breaking medical research.

The Health Data Research Service will be delivered across the UK to provide a single, integrated system for approved researchers across all sectors to access health, social care, and public health data safely. The service will streamline and simplify current processes, ensuring the safety and security of the data, allowing researchers to spend less time talking to different NHS bodies around the country and more time unlocking new insights that will transform our understanding of health.

On 7 April 2025, the Prime Minister announced that the Government and the Wellcome Trust will invest up to £600 million to create a new Health Data Research Service, co-designed through engagement with the public and patients, data users, and stakeholder organisations. This service will bring new treatments and cures to patients by safely enabling the use of patient data to super-charge research, attracting investment and making the United Kingdom one of the best places in the world to conduct ground-breaking medical research.

This groundbreaking initiative will deliver significant health benefits to the UK public and patients across the full spectrum of existing health research, including major public health challenges and diseases such as obesity, cancer, diabetes, and heart disease, which we know disproportionately shorten the lives of people in more deprived communities. The service will be designed to support people to get access to clinical trials and outputs from research faster, and the DigiTrials service supports researchers to recruit people to their trials who represent our diverse population.

At the heart of the Health Data Research Service (HDRS) is a national network of Secure Data Environments, built on the existing NHS Research Secure Data Environment Network, which have been developed in lockstep with their local communities, and which cover the whole of England. The HDRS will bring services together to support fast and secure access to data for researchers, but there is no intention to move existing data assets which sit in various organisations across the nation and require expertise to process, gather, and use, and work will continue with communities to ensure that the service continues to develop with patient and public trust at its heart. We will also be closely working with the devolved administrations to ensure this is a UK wide service, and with the relevant charities to ensure that people from all backgrounds are represented.

We are committed to designing the service in close partnership with patients, professionals, and the public to deliver a trusted service, providing safe and secure access to health, social care, and public data, and to ensure that the research enables the improvement of local service provision and preventative health measures. Detailed design work for this will begin once we have a Chief Executive Officer in place.

NHS England and the Department are running a major national engagement programme on data with over 4,000 people across England. The initial findings and recommendations from the public are already informing our approach and will continue to shape the design and governance of the HDRS. This will support everyone, from medical researchers to health charities, to develop evidence-based solutions to major public health challenges.

On 7 April 2025, the Prime Minister announced that the Government and the Wellcome Trust will invest up to £600 million to create a new Health Data Research Service, co-designed through engagement with the public and patients, data users, and stakeholder organisations. This service will bring new treatments and cures to patients by safely enabling the use of patient data to super-charge research, attracting investment and making the United Kingdom one of the best places in the world to conduct ground-breaking medical research.

This groundbreaking initiative will deliver significant health benefits to the UK public and patients across the full spectrum of existing health research, including major public health challenges and diseases such as obesity, cancer, diabetes, and heart disease, which we know disproportionately shorten the lives of people in more deprived communities. The service will be designed to support people to get access to clinical trials and outputs from research faster, and the DigiTrials service supports researchers to recruit people to their trials who represent our diverse population.

At the heart of the Health Data Research Service (HDRS) is a national network of Secure Data Environments, built on the existing NHS Research Secure Data Environment Network, which have been developed in lockstep with their local communities, and which cover the whole of England. The HDRS will bring services together to support fast and secure access to data for researchers, but there is no intention to move existing data assets which sit in various organisations across the nation and require expertise to process, gather, and use, and work will continue with communities to ensure that the service continues to develop with patient and public trust at its heart. We will also be closely working with the devolved administrations to ensure this is a UK wide service, and with the relevant charities to ensure that people from all backgrounds are represented.

We are committed to designing the service in close partnership with patients, professionals, and the public to deliver a trusted service, providing safe and secure access to health, social care, and public data, and to ensure that the research enables the improvement of local service provision and preventative health measures. Detailed design work for this will begin once we have a Chief Executive Officer in place.

NHS England and the Department are running a major national engagement programme on data with over 4,000 people across England. The initial findings and recommendations from the public are already informing our approach and will continue to shape the design and governance of the HDRS. This will support everyone, from medical researchers to health charities, to develop evidence-based solutions to major public health challenges.

On 7 April 2025, the Prime Minister announced that the Government and the Wellcome Trust will invest up to £600 million to create a new Health Data Research Service, co-designed through engagement with the public and patients, data users, and stakeholder organisations. This service will bring new treatments and cures to patients by safely enabling the use of patient data to super-charge research, attracting investment and making the United Kingdom one of the best places in the world to conduct ground-breaking medical research.

This groundbreaking initiative will deliver significant health benefits to the UK public and patients across the full spectrum of existing health research, including major public health challenges and diseases such as obesity, cancer, diabetes, and heart disease, which we know disproportionately shorten the lives of people in more deprived communities. The service will be designed to support people to get access to clinical trials and outputs from research faster, and the DigiTrials service supports researchers to recruit people to their trials who represent our diverse population.

At the heart of the Health Data Research Service (HDRS) is a national network of Secure Data Environments, built on the existing NHS Research Secure Data Environment Network, which have been developed in lockstep with their local communities, and which cover the whole of England. The HDRS will bring services together to support fast and secure access to data for researchers, but there is no intention to move existing data assets which sit in various organisations across the nation and require expertise to process, gather, and use, and work will continue with communities to ensure that the service continues to develop with patient and public trust at its heart. We will also be closely working with the devolved administrations to ensure this is a UK wide service, and with the relevant charities to ensure that people from all backgrounds are represented.

We are committed to designing the service in close partnership with patients, professionals, and the public to deliver a trusted service, providing safe and secure access to health, social care, and public data, and to ensure that the research enables the improvement of local service provision and preventative health measures. Detailed design work for this will begin once we have a Chief Executive Officer in place.

NHS England and the Department are running a major national engagement programme on data with over 4,000 people across England. The initial findings and recommendations from the public are already informing our approach and will continue to shape the design and governance of the HDRS. This will support everyone, from medical researchers to health charities, to develop evidence-based solutions to major public health challenges.

On 7 April 2025, the Prime Minister announced that the Government and the Wellcome Trust will invest up to £600 million to create a new Health Data Research Service, co-designed through engagement with the public and patients, data users, and stakeholder organisations. This service will bring new treatments and cures to patients by safely enabling the use of patient data to super-charge research, attracting investment and making the United Kingdom one of the best places in the world to conduct ground-breaking medical research.

This groundbreaking initiative will deliver significant health benefits to the UK public and patients across the full spectrum of existing health research, including major public health challenges and diseases such as obesity, cancer, diabetes, and heart disease, which we know disproportionately shorten the lives of people in more deprived communities. The service will be designed to support people to get access to clinical trials and outputs from research faster, and the DigiTrials service supports researchers to recruit people to their trials who represent our diverse population.

At the heart of the Health Data Research Service (HDRS) is a national network of Secure Data Environments, built on the existing NHS Research Secure Data Environment Network, which have been developed in lockstep with their local communities, and which cover the whole of England. The HDRS will bring services together to support fast and secure access to data for researchers, but there is no intention to move existing data assets which sit in various organisations across the nation and require expertise to process, gather, and use, and work will continue with communities to ensure that the service continues to develop with patient and public trust at its heart. We will also be closely working with the devolved administrations to ensure this is a UK wide service, and with the relevant charities to ensure that people from all backgrounds are represented.

We are committed to designing the service in close partnership with patients, professionals, and the public to deliver a trusted service, providing safe and secure access to health, social care, and public data, and to ensure that the research enables the improvement of local service provision and preventative health measures. Detailed design work for this will begin once we have a Chief Executive Officer in place.

NHS England and the Department are running a major national engagement programme on data with over 4,000 people across England. The initial findings and recommendations from the public are already informing our approach and will continue to shape the design and governance of the HDRS. This will support everyone, from medical researchers to health charities, to develop evidence-based solutions to major public health challenges.

On 7 April 2025, the Prime Minister announced that the Government and the Wellcome Trust will invest up to £600 million to create a new Health Data Research Service, co-designed through engagement with the public and patients, data users, and stakeholder organisations. This service will bring new treatments and cures to patients by safely enabling the use of patient data to super-charge research, attracting investment and making the United Kingdom one of the best places in the world to conduct ground-breaking medical research.

This groundbreaking initiative will deliver significant health benefits to the UK public and patients across the full spectrum of existing health research, including major public health challenges and diseases such as obesity, cancer, diabetes, and heart disease, which we know disproportionately shorten the lives of people in more deprived communities. The service will be designed to support people to get access to clinical trials and outputs from research faster, and the DigiTrials service supports researchers to recruit people to their trials who represent our diverse population.

At the heart of the Health Data Research Service (HDRS) is a national network of Secure Data Environments, built on the existing NHS Research Secure Data Environment Network, which have been developed in lockstep with their local communities, and which cover the whole of England. The HDRS will bring services together to support fast and secure access to data for researchers, but there is no intention to move existing data assets which sit in various organisations across the nation and require expertise to process, gather, and use, and work will continue with communities to ensure that the service continues to develop with patient and public trust at its heart. We will also be closely working with the devolved administrations to ensure this is a UK wide service, and with the relevant charities to ensure that people from all backgrounds are represented.

We are committed to designing the service in close partnership with patients, professionals, and the public to deliver a trusted service, providing safe and secure access to health, social care, and public data, and to ensure that the research enables the improvement of local service provision and preventative health measures. Detailed design work for this will begin once we have a Chief Executive Officer in place.

NHS England and the Department are running a major national engagement programme on data with over 4,000 people across England. The initial findings and recommendations from the public are already informing our approach and will continue to shape the design and governance of the HDRS. This will support everyone, from medical researchers to health charities, to develop evidence-based solutions to major public health challenges.