29 Apr 2025·Department of Health and Social Care·Answered
AskedWhat steps he is taking to ensure that planned reforms to social care help tackle barriers for (a) deafblind people and (b) other disabled people with complex needs.
ReplyThe Government recognises the challenges facing the adult social care system, and that people are suffering without the care they need or fighting a complicated system just to receive poor quality care.The independent commission into adult social care, chaired by Baroness Louise Casey, will work with people who draw on care and their families, as well as sector partners, to make clear recommendations for how to rebuild the adult social care system to meet the current and future needs of the population, including for deafblind people and other disabled people with complex needs.At the same time, we are committed to making immediate improvements. We will give disabled people more independence in their own homes through continued investment in the Disabled Facilities Grant (DFG), which funds practical changes that suit individual people’s needs. We have provided an uplift of £172 million across this and the last financial year, bringing the total funding for the DFG to £711 million in 2024/25 and 2025/26.The Government understands the vital importance of coproduction, working directly with people who draw on care and support, including deafblind people and others with complex needs, to design policies that work for them to make their lives better.
29 Apr 2025·Department of Health and Social Care·Answered
AskedWhat steps his Department is taking to reduce regional differences in access to pharmacies.
ReplyFor 2025/26, funding for the core community pharmacy contractual framework has been increased to £3.073 billion. This represents the largest uplift in funding of any part of the National Health Service, over 19% across 2024/25 and 2025/26.The Pharmacy Access Scheme provides additional funding to support pharmacies in areas where there are fewer. Community pharmacies are private businesses that provide NHS funded services. There are 10,407 community pharmacies as of 31 March 2025.Most pharmacies are not directly commissioned or contracted by the NHS, instead contractors apply to gain entry to the NHS pharmaceutical list, and if an application is approved, a pharmacy can open and start providing services.Local authorities are required to undertake a pharmaceutical needs assessment (PNA) every three years to assess whether their population is adequately served by local pharmacies, and must keep these assessments under review. Integrated care boards (ICBs) give regard to the PNAs when reviewing applications from the new contractors. Contractors can also apply to open a new pharmacy to offer benefits to patients that were not foreseen by the PNA. If there is a need for a new local pharmacy to open and no contractors apply to open a pharmacy and fill the gap, ICBs can commission a new pharmacy to open outside of the market entry processes, and fund the contract from ICBs’ budgets.The Pharmacy Access Scheme helps protect access to pharmacies in areas where there are fewer pharmacies and higher health needs, so that no area is left without access to local, physical NHS pharmaceutical services.
29 Apr 2025·Department of Health and Social Care·Answered
AskedWhat steps his Department is taking to increase the number of pharmacies above 10,000.
ReplyFor 2025/26, funding for the core community pharmacy contractual framework has been increased to £3.073 billion. This represents the largest uplift in funding of any part of the National Health Service, over 19% across 2024/25 and 2025/26.The Pharmacy Access Scheme provides additional funding to support pharmacies in areas where there are fewer. Community pharmacies are private businesses that provide NHS funded services. There are 10,407 community pharmacies as of 31 March 2025.Most pharmacies are not directly commissioned or contracted by the NHS, instead contractors apply to gain entry to the NHS pharmaceutical list, and if an application is approved, a pharmacy can open and start providing services.Local authorities are required to undertake a pharmaceutical needs assessment (PNA) every three years to assess whether their population is adequately served by local pharmacies, and must keep these assessments under review. Integrated care boards (ICBs) give regard to the PNAs when reviewing applications from the new contractors. Contractors can also apply to open a new pharmacy to offer benefits to patients that were not foreseen by the PNA. If there is a need for a new local pharmacy to open and no contractors apply to open a pharmacy and fill the gap, ICBs can commission a new pharmacy to open outside of the market entry processes, and fund the contract from ICBs’ budgets.The Pharmacy Access Scheme helps protect access to pharmacies in areas where there are fewer pharmacies and higher health needs, so that no area is left without access to local, physical NHS pharmaceutical services.
28 Apr 2025·Department of Health and Social Care·Answered
AskedHow many NHS staff have left the NHS in (a) Devon & Cornwall and (b) the UK under non-disclosure agreements.
ReplyThe Department does not hold information on the number of National Health Service staff who have left the NHS in Devon and Cornwall or across England under non-disclosure agreements.
24 Apr 2025·Department of Health and Social Care·Answered
AskedWhat assessment he has made of the potential impact of health misinformation on public health decision making.
ReplyThe Department has not made a specific assessment of the impact of health misinformation on public health decision making, but recognises the importance of accurate health information being available to the public and of preventing misinformation.The Department regularly rebuts factual inaccuracies when they appear in traditional media and undertakes extensive planning, engagement, and strategic work to ensure accurate public health information is available on social media channels to mitigate misinformation. In addition, the Department strives to ensure that all of the information it publishes is accurate, clear, and accessible to a variety of audiences, including using easy read versions.
23 Apr 2025·Department of Health and Social Care·Answered
AskedWhat assessment he has made of the potential impact of costs for opticians on trends in the level of people seeking eye care.
ReplyHigh street optical practices are independent businesses that deliver a mix of private and National Health Service eye care services. Free NHS sight tests are available for children, people aged 60 years old and over, individuals on income related benefits, and those at risk of particular eye diseases. The funding for NHS sight tests is demand led, with no limit set on the numbers of NHS sight tests that can be provided. The numbers of NHS sight tests continue to increase, with 13.7 million sight tests provided to eligible groups in 2023/24, and access for NHS patients remains good.Help is also available for eligible patients to assist with the cost of glasses or contact lenses, through NHS optical vouchers. Integrated care boards can also commission primary eye care services over and above the NHS sight testing service from optical practices, where they consider these necessary to meet local need.
23 Apr 2025·Department of Health and Social Care·Answered
AskedWhat assessment he has made of the potential impact of additional costs incurred during eye tests on low income households attending opticians.
ReplyFree National Health Service sight tests are available to individuals on income-related benefits, and help is also available through the NHS low income scheme. An ophthalmic practitioner is required to undertake any clinically necessary tests to determine if a patient has any signs of injury, disease, or abnormality, and to refer the patient for any necessary further investigations. Therefore, no patient receiving a sight test under the NHS is required to incur any additional costs.Additionally, NHS optical vouchers to help towards the cost of glasses or contact lenses are available for eligible groups, including people on income-related benefits, and through the NHS low-income scheme. Patients can use their voucher to purchase their optical appliance from a supplier of choice, and there are providers who offer a range of glasses within voucher value.
17 Apr 2025·Department of Health and Social Care·Answered
AskedIf he will take steps to amend the Care Act 2014 to exempt infected blood compensation scheme payments from (a) residential and (b) domiciliary care charges.
ReplyMy Rt. Hon. Friend, the Secretary of State for Health and Social Care, does not consider that the Care Act 2014 needs to be amended to exempt Infected Blood Compensation Scheme payments because, under the Care and Support (Charging and Assessment of Resources) Regulations 2014, local authorities must disregard any payments from an approved blood scheme when carrying out a financial assessment relating to charges for residential or non-residential care. An approved blood scheme is a scheme approved by the Secretary of State, or trust established with funds provided by the Secretary of State, to provide compensation in respect of a person having been infected from contaminated blood or blood products. The Infected Blood Compensation Scheme as set out in the Infected Blood Compensation Scheme Regulations 2024 is an approved blood scheme.
8 Apr 2025·Department of Health and Social Care·Answered
AskedWhat information his Department holds on (a) when the Medicines and Healthcare products Regulatory Agency plans to publish guidance on regulatory process for phage therapy use; and (b) whether that guidance will help reduce regulation on phage therapy research.
ReplyThe Medicines and Healthcare products Regulatory Agency (MHRA) is preparing the draft guidance, Regulatory considerations for therapeutic use of bacteriophages in the United Kingdom, which will be published in the second quarter of 2025.Regulation of medicines in the UK is undertaken by the MHRA in accordance with the Human Medicines Regulations 2012 (SI 2012/1916) (as amended), thereby ensuring compliance with statutory obligations relating to the manufacture, distribution, sale, labelling, advertising, and promotion of medicines.The purpose of the guidance is to address regulatory considerations applicable to the use, in the UK, of bacteriophages for therapeutic purposes in humans, whether as licensed or unlicensed medicinal products.
8 Apr 2025·Department of Health and Social Care·Answered
AskedPursuant to the Answer of 2 April 2025 to Question 41337 on Dangerous Dogs, what steps he is taking to improve health outcomes for people who are victims of dog bites.
ReplyThe National Health Service provides advice on what to do after an animal bite, which is available at the following link:https://www.nhs.uk/conditions/animal-and-human-bites/Individuals who have been bitten by an animal and are concerned should seek medical assistance.
8 Apr 2025·Department of Health and Social Care·Answered
AskedIf he will take steps with Versus Arthritis to improve the quality of data that his Department publishes on arthritis.
ReplyThe Department of Health and Social Care will continue to work with Versus Arthritis as we consider how best to support people with musculoskeletal (MSK) conditions such as arthritis. Data on MSK health, including arthritis, is published on Fingertips, and is available at the following link:https://fingertips.phe.org.uk/profile/msk/dataIntegrated care boards (ICBs) are responsible for commissioning services that meet the needs of their populations. To support this, the Department of Health and Social Care is delivering the Getting It Right First Time MSK Community Delivery Programme jointly with NHS England and the Department for Work and Pensions. With a £3.5 million funding boost as part of the programme, ICBs will assess their current MSK services and share examples of best practice, roll out innovative ways of working, as well as improving data on how services are performing.The implementation of Secure Data Environments (SDEs), allowing National Health Service data to be accessed through secure platforms rather than shared with researchers, will support safer and more secure access to health and care data for secondary uses, such as research into prevalence and impact. This is being delivered through major investment in digital infrastructure across the NHS in England, including the NHS Research SDE Network, funded by the Data for Research and Development programme.The Single Patient Record will also give clinicians in different settings access to comprehensive records on a person's health, so that they have the information they need to make the best-informed decisions when delivering care and treatment.
3 Apr 2025·Department of Health and Social Care·Answered
AskedIf he will make a comparative assessment of the effectiveness of phage therapy regulatory frameworks in (a) Belgium, (b) Canada, (c) France, (d) the US and (e) Australia; whether he plans to adopt similar measures in the UK; and if he will make an assessment of the potential impact of doing so on patient access.
ReplyThe United Kingdom’s regulatory framework supports patient access to phage therapy and is in line with many other national regulatory authorities. We continue to keep the regulatory framework for phage therapies under review, aligning where necessary with regulatory frameworks internationally, in order to support continued patient access via phage sharing between countries.The Medicines and Healthcare products Regulatory Agency is planning to publish draft guidance on phage product licensing, developed with researchers and industry, to clarify regulatory and manufacturing requirements.
3 Apr 2025·Department of Health and Social Care·Answered
AskedWhether his Department is taking steps to simplify the process for clinicians seeking approval to use phage therapy.
ReplyIn March 2024, the Government’s response to the Science, Innovation and Technology Committee’s report on bacteriophages highlighted the potential role of phage therapy as one of a range of tools to tackle antimicrobial resistance.To support clinical use, the Medical and Healthcare Products Regulatory Agency plans to publish non-mandatory guidance on the quality, safety, and efficacy data required to license phage products for both proactive and reactive National Health Service use to treat common infections, and the National Institute for Health and Care Excellence will assess new phage-based treatments alongside other medicines.
3 Apr 2025·Department of Health and Social Care·Answered
AskedIf he will bring forward legislative proposals to introduce a magistral phage model to allow UK phages to be produced without requiring GMP licensing.
ReplyIn its March 2024 response to the Science, Innovation and Technology Committee’s report on bacteriophages, the Government acknowledged the challenges in manufacturing phage materials in the United Kingdom, including the requirement to meet Good Manufacturing Practice (GMP) standards. The principles of GMP are considered necessary to ensure the medicines are of the appropriate quality, safety, and efficacy. The Government committed to considering the case for the development of a UK-based GMP facility to support phage innovators.In parallel, the Government is engaging with professional regulators and the specialist pharmacy service to clarify how existing regulations address liability for the use of non-GMP produced phages. Unlicensed phages can currently be used in the UK for compassionate cases with appropriate controls. The Medicines and Healthcare products Regulatory Agency will be publishing regulatory considerations for therapeutic use of bacteriophages in the UK in the second quarter of 2025, which will offer guidance on these matters.
3 Apr 2025·Department of Health and Social Care·Answered
AskedWhether he plans to make an assessment of the (a) adequacy of the requirement for UK-produced phages to be manufactured under good manufacturing practice and (b) potential impact of this requirement on patient access to treatment.
ReplyIn the March 2024 response to the Science, Innovation and Technology Committee’s report on bacteriophages, the Government acknowledged the challenges of requiring United Kingdom-produced phages to meet Good Manufacturing Practice (GMP) standards, which is essential for clinical use.To address this, the Government committed to exploring the case for a dedicated GMP facility to support phage innovators, working with key stakeholders, including funders and research organisations, to strengthen the UK’s phage manufacturing capabilities and thereby improve patient access to these therapies.
3 Apr 2025·Department of Health and Social Care·Answered
AskedWhat assessment his Department has made of the potential impact of the level of imports of phage products on national security; and whether he is taking steps to help develop UK-based manufacturing capabilities.
ReplyIn the March 2024 response to the Science, Innovation and Technology Committee’s report on bacteriophages, the government acknowledged the challenges in developing phage therapy in the United Kingdom, including the requirement to meet Good Manufacturing Practice (GMP) standards. GMP is the minimum standard that a medicines manufacturer must meet in their production processes. To meet GMP, products must:- be of consistent high quality;- be appropriate to their intended use; and- meet the requirements of the marketing authorisation or product specification.In the response, the Government committed to considering the case for a UK-based GMP facility to support phage innovators and reduce reliance on imports. The UK Health Security Agency is also exploring phage production options in accordance with GMP, working with partners nationally and internationally.The new Life Sciences Sector Plan, part of the upcoming Industrial Strategy, to be published in late spring 2025, will outline the Government’s growth strategy for the sector. Within this, domestic manufacturing, including for bacteriophage production, is a priority and projects can be supported via applications to the Life Sciences Innovative Manufacturing Fund.In parallel, the Medicines and Healthcare products Regulatory Agency will be publishing draft guidance on phage product licensing, developed with researchers and industry, to clarify regulatory and manufacturing requirements.
3 Apr 2025·Department of Health and Social Care·Answered
AskedIf he will make an assessment of the potential merits of introducing a phage impact bond that is similar to previous social impact bonds.
ReplySocial Impact Bonds (SIBs) are a mechanism to raise investment for a service provider. SIBs are commissioned on a payment-by-results basis, with the payment being proportional to the delivery of a positive social outcome.As detailed in the Government’s response to the Science, Innovation and Technology Committee’s report on bacteriophages, published 1 March 2024, the Government is focusing on projects that aim to be most beneficial to supporting phage development in the United Kingdom, based on an assessment of context and barriers.This includes exploring the case for a dedicated Good Manufacturing Practice facility to support phage innovators, working with key stakeholders, including funders and research organisations, to strengthen the UK’s phage manufacturing capabilities and thereby improve patient access to these therapies.Currently, SIBs have not been identified as a mechanism that would progress development beyond the impact of current projects, but will be considered alongside other options.
2 Apr 2025·Department of Health and Social Care·Answered
AskedIf his Department will work with Versus Arthritis to improve work-related support for people with arthritis.
ReplyThe Department will continue to work with Versus Arthritis as we consider how best to address ill-health related economic inactivity, including improving work-related support for people with musculoskeletal (MSK) conditions such as arthritis.The Get Britain Working White Paper set out that the Government is investing £240 million to tackle the root causes behind why people are not working and join up help and support, based on the needs of local people and places.In terms of the wider provision of work-related support for people with MSK, and as part of the localism agenda, the WorkWell service is piloting low-intensity work and health support. This support is led by local partnerships of health systems, local authorities, and job centres in 15 areas of England. By spring 2026, WorkWell pilots aim to support 56,000 disabled people and people with health conditions, including MSK conditions, to get into work and to get on at work.The Government is also mobilising eight inactivity trailblazers in England and Wales that will lead the way in delivering a joined-up local work, health and skills offer. Three of these areas will receive a share of £45 million to become Health and Growth Accelerators. The Accelerators will focus on prevention and early intervention to improve population health outcomes and reduce health-related economic inactivity. MSK is one of the key drivers of health-related inactivity and integrated care boards will consider targeted interventions as part of their plans.
2 Apr 2025·Department of Health and Social Care·Answered
AskedIf his Department will work with Versus Arthritis to increase funding in musculoskeletal research.
ReplyThe Department funds health and care research through the National Institute for Health and Care Research (NIHR). The NIHR funds clinical, public health and social care research and works in partnership with the National Health Service, charities, universities, local government, other research funders, patients, and the public.The NIHR supports and delivers research across a variety of musculoskeletal conditions such as arthritis, which includes osteo, rheumatoid, psoriatic and juvenile arthritis, osteoporosis and joint and back pain. In 2023/24, the NIHR funded £17.3 million in musculoskeletal research.The NIHR works in collaboration with Versus Arthritis on a joint initiative, the UK Musculoskeletal (MSK) Translational Research Collaboration, aligning investment in MSK translational research, and creating a United Kingdom-wide ambition and focus to drive cutting edge research and improve outcomes for patients.The NIHR welcomes funding applications for research into any aspect of human health, including arthritis and other musculoskeletal conditions through its research programmes.
2 Apr 2025·Department of Health and Social Care·Answered
AskedIf his Department will work with Versus Arthritis to improve (a) care and (b) support for young people with arthritis.
ReplyOn 6 January 2025, NHS England published the new Elective Reform Plan, which sets out a whole system approach to hitting the 18-week referral to treatment target by the end of this Parliament.Integrated care boards (ICBs) are responsible for commissioning services that meet the needs of their populations, including for those with arthritis. To support this, the Department of Health and Social Care is delivering the Getting It Right First Time (GIRFT) Musculoskeletal (MSK) Community Delivery Programme jointly with NHS England and the Department for Work and Pensions. With a £3.5 million funding boost, GIRFT will work with the ICBs to reduce MSK community waiting times.The Department funds research into MSK conditions, including arthritis, through the National Institute for Health and Care Research (NIHR). Through that route, the Department spent approximately £26.3 million on MSK research in 2023/24, and £79.2 million since 2019/20. In particular, the Leeds Biomedical Research Centre aims to improve treatment for osteoarthritis. The NIHR, in collaboration with Versus Arthritis, also funds a dedicated UK MSK Translational Research Collaboration, aligning investment in MSK translational research and creating a United Kingdom-wide ambition and focus to drive cutting edge research and improve outcomes for patients.The GIRFT programme in NHS England has had a paediatric rheumatology workstream since April 2024. The team has assembled the largest ever set of data and information about paediatric rheumatology in England and is visiting every department in England to discuss its findings. It will produce its national report with recommendations later this financial year. This will include a focus on supporting young people and their parents as they transition to adult services.The GIRFT team will be working with the British Society for Rheumatology and rheumatology departments in England to implement the findings and recommendations of the GIRFT paediatric rheumatology national report.NHS England Specialised Commissioning has a Clinical Reference Group for specialised paediatric rheumatology, which has produced a service specification naming juvenile idiopathic arthritis as one of the conditions that should be managed by a specialist paediatric rheumatology team. The service specification also sets out that specialised paediatric rheumatology teams will provide transitional care to facilitate transfer to, and ongoing care in, adult rheumatology. Specialised paediatric rheumatology services are expected to be commissioned in line with this service specification.The Department will continue to work with Versus Arthritis as we consider how best to provide National Health Services for people with MSK conditions such as arthritis.