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About the GPDPR programme

An overview of the programme, our approach and the journey so far.

Listening, learning and doing things better

During the summer of 2021 substantial public, patient and professional concerns were raised about the changes we were proposing to improve the control, security, and consistency of access to data from general practice (GP). Many of these people, including GPs, also think that in the past these concerns had not been listened to or fully understood. We, as a health and care system, have an opportunity through this new GP data collection, ‘GP Data for Planning and Research’ to do much better.

We know we need to listen, understand, engage and act on what we learn to get this right, and we are committed to doing so. We are redesigning the programme from the ground up and are spending time working with partners such as, health and care professionals including the Royal College of GPs, research organisations and patient charities, data experts and the National Data Guardian, patients and the public to establish how best to address the concerns raised. We have listened to some critical feedback and we promise to work more closely with our partners to make sure they are confident that data is kept secure, the workload for general practice staff is reduced so they can concentrate on patients, and to communicate better with everyone. 

We do not have a set start date for this collection and will only do so when we, and our partners, are confident that we have engaged, listened, learned and made changes as a result.

We will only begin to collect data when: 

  • the British Medical Association (BMA), Royal College of General Practitioners (RCGP) and the National Data Guardian (NDG) are satisfied with the proposed arrangements - they are working with us as part of our Check and Challenge Group and will be key partners throughout the design process
  • an effective, secure computing environment (known as a Trusted Research Environment) has been developed to allow approved researchers to access data they have applied for, without it ever being copied or moved outside the security of the NHS 
  • any previous data collected through the GP Data for Planning and Research collection can be deleted at any time if people choose to opt-out of sharing their GP data with us
  • people are more aware of the new data collection process as a result of wider engagement and communication

Why we need a new GP data collection system

Data about patients has been used for over 40 years to develop new treatments for disease, to make sure that local communities have the health services they need and to plan national services, for example to make sure that we train the right numbers of doctors and nurses, and that hospitals are seeing cancer patients within two weeks of being referred by their GP, or if patients with diabetes are receiving the vital checks that help to manage their condition.

The system that collects GP data is over 10 years old and needs to be replaced. The new service replaces 300 individual collections with one single collection. This is more efficient, with stronger privacy protections for the data at all stages and reduces the burden on general practices. For these reasons we are developing a new way to collect this data, working with general practice, patients and the public and data experts, to develop a solution which is safe, trusted and which maintains privacy. This project is called GP Data for Planning and Research.

Building trust through transparency - our communications approach

The General Practice Data for Planning and Research programme has developed a 5-phase communication plan which will: 

  1. Define the scope of the communication and engagement approach
  2. Listen to people’s views and concerns 
  3. Engage and involve the public, patients and health professionals in shaping the approach
  4. Demonstrate how we have responded to what we have heard 
  5. Ensure the public is well informed about the improvements. 

Here you’ll find more detail on how we’re working to deliver on these commitments.


Engaging with key stakeholders to improve and assure the communication and engagement approach for the programme. In this phase, we will inform stakeholders of our planned approach, listen to their feedback and amend the communications workstream plan to accommodate those changes. We will also use this opportunity to seek buy-in from stakeholders and demonstrate transparency and listening in our work.

Read the assurance phase report.


We will listen to a wide range of people to gather views and understand their needs and concerns, building on the valuable information that has previously been shared with us. This will be used to inform the policy decisions, technology, processes, and our engagement and communications activity. 

We have already developed a number of assurance groups to enable us to regularly meet with interested parties and to check our thinking as the programme develops. These groups will publish action notes and you can learn more about their Terms of Reference and membership on the dedicated pages.

We are always open to feedback as we develop the programme and anyone can contact us via [email protected] to give their views.

Read our listening phase report.


We will run a series of events offering opportunities to talk with a broad range of people, such as patients and GP practice staff. We will explain the data collection, answer questions, and work together to ensure that what the programme develops meets their needs.


We will show how the feedback we have gathered during both the Listening phase and the Engagement phase has been used to help design the technology, processes, and communication materials.


The new systems and processes that we have developed, informed by the earlier phases, will be launched. These will be supported in advance by information for NHS staff and the public about the data collection, their right to opt out, as well as how to change their choice if they wish to.

We have not set fixed timescales for each phase because the lessons learned in each one will need to shape the next. We are currently planning the listening phase and will publish further information about this shortly. We will ensure that we reach people from different backgrounds, including those that are digitally excluded.

Continuing the conversation - keeping you informed

We will provide regular updates about our work to make sure that people are informed about our progress and how they can get involved. 

See regular updates from the assurance groups here:

We also publish regular blogs about the programme, which you can read here:

Keeping data safe – the right people, with the right access, at the right time

Trusted Research Environment (TRE) is a new and secure way to provide approved researchers with access to the data they need for ethically and legally approved research projects. The data is accessed in a secure location rather than being downloaded and is de-identified to make sure that patients cannot be identified.

The use of the data is tracked and no data can leave the secure environment, providing greater assurance that sensitive data is handled securely.

Organisations requesting controlled access to this data must have a specific reason to need the data which benefits health and care, and a clear legal basis for access. Only the minimum amount of data needed to meet the specific purpose will be accessible.

We will not develop our TRE alone and we know that we need to take on board the views of clinicians and data experts. We will seek advice from the Independent Group Advising on the Release of Data (IGARD) and from the GP Profession Advisory Group (PAG) to make sure that the highest standards of governance are upheld. Information about all of the data that we have shared since 2012 is published in our data uses register.

We will never approve requests to access data where the purpose is for marketing purposes, including promoting or selling products or services, market research, insurance or advertising or any other solely commercial purpose. Find out more about how we make decisions about data access, including the independent experts that we ask for advice.

More information about TRE can be found on the Understanding Patient Data website.

Last edited: 22 March 2023 12:32 pm