Speeches made during Parliamentary debates are recorded in Hansard. For ease of browsing we have grouped debates into individual, departmental and legislative categories.
These initiatives were driven by Lord Campbell-Savours, and are more likely to reflect personal policy preferences.
MPs who are act as Ministers or Shadow Ministers are generally restricted from performing Commons initiatives other than Urgent Questions.
Lord Campbell-Savours has not been granted any Urgent Questions
Lord Campbell-Savours has not been granted any Adjournment Debates
Lord Campbell-Savours has not introduced any legislation before Parliament
Lord Campbell-Savours has not co-sponsored any Bills in the current parliamentary sitting
The Government is committed to promoting fairness and transparency for homeowners and ensuring that consumers are protected from abuse and poor service. We have already committed to setting a maximum fee and timescale for the provision of leasehold information when a home is being sold. This will require freeholders, or managing agents acting on their behalf, to provide relevant information including details of service charges. We will bring forward these proposals as soon as parliamentary time allows and will publicise changes widely so that leaseholders are aware of the maximum fee they should pay.
Furthermore, as set out in the Levelling Up White Paper, the UK Government and the industry will work together to ensure the critical material information buyers of leasehold and freehold properties need to know - like tenure type, lease length and any service charges - are available digitally wherever possible from trusted and authenticated sources, and provided only once.
The Valuation Office Agency's "Check your council tax band" online service shows that there are two properties liable for council tax on Downing Street. Both properties are in band H. Council tax decisions are taken by local authorities, but information published by Westminster City Council shows that the band H charge for 2021-22 is £1655.12, including the precept for the Greater London Authority.
The Prime Minister’s letter to the CEO of the Restoration and Renewal Delivery Authority and the CEO of the R&R Sponsor Body, which requests that it give consideration to decant locations outside of London, were deposited in the Libraries of both Houses on 15 July. This letter is also publicly available on the parliamentary website.
The Government is keen to ensure the R&R of the Palace of Westminster delivers best value for money and would like the Sponsor Body to advise Parliament regarding a range of options as part of this process. As per the principle of exclusive cognisance, the location of Parliament is a matter for Parliament itself.
The Senior Deputy Speaker has asked me, as Chair of the Services Committee, to respond on his behalf. Trimble Manhattan Space Scheduling (Trimble) are engaged by Parliament to provide room booking software utilised by the Attendants office in managing meeting and committee rooms.
This contract has been held by the Parliamentary Digital Service (PDS) since 1 August 2012 and to date £95,536 has been spent. It is due to expire on 28 December 2020 and no further spend is expected on this contract.
Spend over the last four years with Trimble:
Financial Year 2016/17 spend - £0;
Financial Year 2017/18 spend - £23,868 (PDS);
Financial Year 2018/19 spend - £11,506 (PDS);
Financial Year 2019/20 spend - £7,956 (PDS).
The only parliamentary contract awarded to Trimble in the last four years is held by the Commons Northern Estate Programme (NEP).
A candidate does not have to report evidence of their disability in order to use the exemption brought forward by The Police and Crime Commissioner Elections (Amendment) Order 2020. This upholds the confidentiality of the candidate and is consistent with disability exemptions in place for elections across the UK, including UK Parliamentary general elections.
A candidate will need to make an assessment as to whether their disability meets the definition of disability provided in the 2020 Order. This uses the definition of disability contained within the 2010 Equality Act. There is also statutory guidance available on the meaning of disability under the Equality Act which should help candidates undertake this assessment.
The UK has a robust regulatory system which provides a comprehensive regime for exploration and production activities in the offshore oil and gas sector, which includes provisions to ensure safe operations and protect the environment. The legislation allows the Government to serve legal notices on any party involved in the exploration and production of an offshore oil or gas field, ensuring they remain responsible for decommissioning costs, rather than the UK taxpayer.
Offshore operators will require environmental permits from the relevant environment agencies, scrutiny by the relevant health and safety bodies, and Oil and Gas Authority consents for drilling under the provisions of their licence.
All Local Enterprise Partnerships (LEPs) are subject to mid-year and annual performance reviews that consider areas of governance, delivery performance, and strategic impact. The York and North Yorkshire (YNY) LEP was considered to have met the requirements in all three areas following its 2020-21 annual performance review. The delivery assessment took account of YNY LEP’s overall performance in delivering its Local Growth and Getting Building Fund programmes, including progress on the delivery of Askham Bryan projects being funded from these programmes.
In order to provide assurance on the robust stewardship of public funds and to meet governance performance requirements, LEPs are required to develop a local assurance framework that meets the mandatory governance, accountability, and transparency requirements set out in the National Local Growth Assurance Framework.
In so doing, LEPs must put in place appropriate data protection arrangements in line with the Data Protection Act 1998, the General Data Protection Requirements (GDPR), and the Data Protection Act 2018. YNY LEP is the data controller for data they collect including any relating to Askham Bryan College. The LEP should ensure it follows the appropriate procedures and that internal processes are compliant with the legislation.
LEPs are also required to have a legal personality and must abide by the laws and regulations that apply to the legal entity they adopt. YNY LEP is a private company limited by guarantee without share capital.
The then York, North Yorkshire, and East Riding (YNYER) Local Enterprise Partnership (LEP) received local growth funding of £145.9m awarded in three rounds, announced in July 2014, January 2015, and January 2017. The funds were to be spent between financial years 2015-16 and 2020-21.
Funding awards were based on consideration of local Strategic Economic Plans (SEPs), developed by each LEP. Creating skilled and inspired people was a priority in the YNYER SEP and local growth funding supported investment in agri-tech and land-based engineering facilities at Askham Bryan College, as well as a digital farm hub at the College.
A condition of local growth funding allocations to LEPs was that all projects were subject to business cases that met an agreed local Assurance Framework including representing value for money to the taxpayer, being deliverable, and having a strong strategic fit. All LEP investments and investment decisions are publicly available on LEP websites, as the Assurance Framework requires.
In 2020, the Government announced the £900 million Getting Building Fund (GBF) to deliver jobs, skills, and infrastructure across the country. LEPs and Mayors were invited to propose shovel-ready infrastructure projects that would boost economic growth, and fuel local recovery and jobs. Funding awards were based on a consideration of the strategic fit and deliverability of each project. The £15.4m GBF award for the geographically reformed York and North Yorkshire LEP included support for a Digital Skills Academy at Askham Bryan College, again subject to a business case meeting the requirements of the LEP’s local assurance framework as outlined above.
The rules for provision of information by Local Enterprise Partnerships on their allocations to grant and loan applicants are set out in the National Local Growth Assurance Framework, which was published in January 2019.
This Framework provides the Department, Government, stakeholders and the public with the necessary assurances that LEPs have the policies and processes in place to ensure the robust stewardship of public funds. Specifically, it requires LEPs to publish bids and undertake a clear process of recording decisions reached and communicating these in a timely fashion to the applicant.
The UK Government has secured early access to 457 million vaccines doses through agreements with eight separate vaccine developers. This includes agreements with BioNTech/Pfizer, University of Oxford/AstraZeneca, GlaxoSmithKline/Sanofi Pasteur, Novavax, Janssen, Valneva, Moderna and CureVac.
In addition to the above, we have also funded fill and finish capability through a contract with Wockhardt in Wrexham, North Wales, as well as the expansion of the Valneva factory in Livingston, Scotland.
The Vaccine Manufacturing and Innovation Centre (VMIC) should be partially open in summer 2021, with the facility fully operational in 2022. The VMIC is working towards having fill-finish capability by the end of 2021. The objective remains to accelerate the readiness of the VMIC by a year and we are on track to achieve this.
The £38 million investment announced on 17 May 2020 has since been revised because it was superseded following supply agreements with vaccine candidates. Therefore, the costs were limited to the equipment and the knowledge transfer. The Government has committed £8.75 million towards the rapid deployment facility which is now operational and manufacturing the University of Oxford/AstraZeneca vaccine.
The estimated vaccine production manufacturing capacity of the Vaccines Manufacturing and Innovation Centre will be up to 70 million doses of vaccine within six months, once it has opened.
Contracts between the Government and companies developing and producing COVID-19 vaccines will be published in due course.
Contracts between the Government and companies developing and producing COVID-19 vaccines will be published in due course.
The Government has engaged in strategic procurement activity to ensure that we have the necessary ultra-low cold chain capacity needed for the storage and distribution of our portfolio of COVID-19 vaccines.
The UK has a sufficient number of glass vials available, due to orders already placed.
The Government has not entered into a contract with any of the named companies.
The Government has invested in a portfolio of COVID-19 vaccines across a range of modalities to secure UK access to the most promising candidates.
The clinical trials of these vaccines involve testing their safety and efficacy across a range of scenarios, including testing efficacy rates of both single and multi-dose delivery methods.
This will ensure the UK has early access to those vaccines that offer the most protection against COVID-19.
Askham Bryan College’s application for capital funds to support the development of a calf and grower teaching building for cattle was included in the Yorkshire and Humber Institute of Technology proposal which was submitted on 21 November 2018.
The Yorkshire and Humber Institute of Technology proposal was approved on 7 November 2019.
Within the Yorkshire and Humber Institute of Technology proposal, Askham Bryan College were approved to receive £1,746,448 capital funds.
Askham Bryan College have been paid £489,880 to date. The balance of funding, £1,256,568, is due to be paid in this financial year (2021/22).
The Further Education Commissioner and the Education and Skills Funding Agency (ESFA) carried out a comprehensive analysis of local provision needs for Newton Rigg and the surrounding area in 2020. The core objective of this analysis was to establish if there was a need for college provision within the general vicinity of the Newton Rigg campus. It considered the location of neighbouring further education (FE) colleges in relation to travel to learn options and identified that most enrolments could be accommodated at other statutory FE institutions.
In total, 286 16 to 18 year-old students were enrolled onto land based further education courses at Newton Rigg, of which 70 were in residential accommodation. Where gaps in provision were identified, specifically agricultural provision, alternative arrangements for the next academic year have been agreed with Myerscough College in partnership with Ullswater Community College to ensure continuity of delivery of this provision in the Penrith area after Newton Rigg closes.
Both the Further Education Commissioner and the ESFA continue to have regular meetings with the senior leadership team at Askham Bryan College, and this includes, but is not exclusively related to, matters concerning the closure of Newton Rigg Campus.
During the analysis of local provision needs and subsequently the strategic review, the Further Education Commissioner, with support from the ESFA, has engaged with a significant number of stakeholders who had an interest in Newton Rigg, the implications of its proposed closure and the delivery of FE, including land-based provision within Cumbria. This included Cumbria County Council, Eden District Council, Cumbria Local Enterprise Partnership, all statutory FE colleges located within Cumbria, Scotland’s Rural College, the University of Cumbria, University of Central Lancashire, Lancaster University, National Farmers Union, Friends of Newton Rigg, current and former governors of Askham Bryan College and a range of industry stakeholders.
The strategic review commenced in July 2020 and completed in February 2021. This review engaged with local interested parties and all the educational institutions identified above to ascertain interest and options available to maintain specialist provision at the Newton Rigg campus. No suitable alternative solution was identified to maintain education provision at that site.
Following the decision by the University of Cumbria in 2010, to cease delivering the provision of further education funded by the Skills Funding Agency and the Young People’s Learning Agency, the Skills Funding Agency led an open and competitive procurement process, in accordance with Part B of Schedule 3 of the Public Contracts Regulations 2006, to secure an alternative provider or providers for the delivery of arts provision in Carlisle and predominately land-based provision at Newton Rigg. As a result of this competition, the funding for students studying further education at the University’s Brampton Road building was transferred to Carlisle College, and the funding for students studying further education at Newton Rigg, together with the further education assets at Newton Rigg, was transferred to Askham Bryan College. The procurement was subject to a review by Cabinet Office in 2011 and its findings have been published on gov.uk and are attached.
The successor organisation to the Skills Funding Agency, the Education and Skills Funding Agency now procure provision in accordance with the requirements of the Public Contracts Regulations, 2015. In some circumstances, for example the provision of education and training for young people, separate arrangements apply, but processes and procedures are fair and transparent. Where this applies, we use a mix of local negotiation and tendering appropriate to the circumstances in each case.
The government has no plans to publish documents concerning the funding and transfer of assets and land relating to the University of Cumbria’s acquisition of Newton Rigg College in 2007.
Askham Bryan College’s primary relationship with government is with the department and its executive agency, the Education and Skills Funding Agency. The department has overall responsibility for policies relating to the delivery of further education and higher education which are provided by Askham Bryan College.
The Newton Rigg Strategic Review process has been extended. The Further Education Commissioner team and Education and Skills Funding Agency officials are continuing to work closely with stakeholders, including Askham Bryan College, to try and find a solution for retaining some or all of the education provision on the Newton Rigg campus.
Askham Bryan College is independent of the government and is responsible for any decision on Newton Rigg and the associated financial implications.
The Newton Rigg Strategic Review process has been extended. The Further Education Commissioner team and Education and Skills Funding Agency officials are continuing to work closely with stakeholders, including Askham Bryan College, to try and find a solution for retaining some or all of the education provision on the Newton Rigg campus.
Askham Bryan College is independent of the government and is responsible for any decision on Newton Rigg and the associated financial implications.
On 8 April 2021, we published our response to the call for evidence on the need for standards for bio-based, biodegradable and compostable plastics: www.gov.uk/government/consultations/standards-for-biodegradable-compostable-and-bio-based-plastics-call-for-evidence.
While neither a specific assessment of oxo-biodegradable plastic sheeting used by farmers, nor an assessment comparing bio-based resin from starch and lactic acid in biodegradable products used in agriculture to oxo-biodegradable plastics has been made, the aforementioned call for evidence covered oxo-biodegradable plastics.
The Government response acknowledges that there is currently insufficient evidence demonstrating that oxo-biodegradable plastics perform as claimed and biodegrade, without residue, in a reasonable timeframe in the open environment. We continue to monitor the latest developments and evidence and are keen to see research published in international peer reviewed journals illustrating how these plastics degrade in the marine environment, open environment, and under the soil, specifically under naturalistic conditions, as opposed to experimental models of aging. We also welcome further research on the full environmental impacts of using bio-based plastics.
Over the coming months, we intend to commission a research project to further consider the evidence that has been supplied to the call for evidence within the context of wider literature and new research.
We do not plan to make representations to the European Commission on the usability and safety of oxo-biodegradable products in the farming industry.
On 8 April 2021, we published our response to the call for evidence on the need for standards for bio-based, biodegradable and compostable plastics: www.gov.uk/government/consultations/standards-for-biodegradable-compostable-and-bio-based-plastics-call-for-evidence.
While neither a specific assessment of oxo-biodegradable plastic sheeting used by farmers, nor an assessment comparing bio-based resin from starch and lactic acid in biodegradable products used in agriculture to oxo-biodegradable plastics has been made, the aforementioned call for evidence covered oxo-biodegradable plastics.
The Government response acknowledges that there is currently insufficient evidence demonstrating that oxo-biodegradable plastics perform as claimed and biodegrade, without residue, in a reasonable timeframe in the open environment. We continue to monitor the latest developments and evidence and are keen to see research published in international peer reviewed journals illustrating how these plastics degrade in the marine environment, open environment, and under the soil, specifically under naturalistic conditions, as opposed to experimental models of aging. We also welcome further research on the full environmental impacts of using bio-based plastics.
Over the coming months, we intend to commission a research project to further consider the evidence that has been supplied to the call for evidence within the context of wider literature and new research.
We do not plan to make representations to the European Commission on the usability and safety of oxo-biodegradable products in the farming industry.
On 8 April 2021, we published our response to the call for evidence on the need for standards for bio-based, biodegradable and compostable plastics: www.gov.uk/government/consultations/standards-for-biodegradable-compostable-and-bio-based-plastics-call-for-evidence.
While neither a specific assessment of oxo-biodegradable plastic sheeting used by farmers, nor an assessment comparing bio-based resin from starch and lactic acid in biodegradable products used in agriculture to oxo-biodegradable plastics has been made, the aforementioned call for evidence covered oxo-biodegradable plastics.
The Government response acknowledges that there is currently insufficient evidence demonstrating that oxo-biodegradable plastics perform as claimed and biodegrade, without residue, in a reasonable timeframe in the open environment. We continue to monitor the latest developments and evidence and are keen to see research published in international peer reviewed journals illustrating how these plastics degrade in the marine environment, open environment, and under the soil, specifically under naturalistic conditions, as opposed to experimental models of aging. We also welcome further research on the full environmental impacts of using bio-based plastics.
Over the coming months, we intend to commission a research project to further consider the evidence that has been supplied to the call for evidence within the context of wider literature and new research.
We do not plan to make representations to the European Commission on the usability and safety of oxo-biodegradable products in the farming industry.
On 8 April 2021, we published our response to the call for evidence on the need for standards for bio-based, biodegradable and compostable plastics: www.gov.uk/government/consultations/standards-for-biodegradable-compostable-and-bio-based-plastics-call-for-evidence.
While neither a specific assessment of oxo-biodegradable plastic sheeting used by farmers, nor an assessment comparing bio-based resin from starch and lactic acid in biodegradable products used in agriculture to oxo-biodegradable plastics has been made, the aforementioned call for evidence covered oxo-biodegradable plastics.
The Government response acknowledges that there is currently insufficient evidence demonstrating that oxo-biodegradable plastics perform as claimed and biodegrade, without residue, in a reasonable timeframe in the open environment. We continue to monitor the latest developments and evidence and are keen to see research published in international peer reviewed journals illustrating how these plastics degrade in the marine environment, open environment, and under the soil, specifically under naturalistic conditions, as opposed to experimental models of aging. We also welcome further research on the full environmental impacts of using bio-based plastics.
Over the coming months, we intend to commission a research project to further consider the evidence that has been supplied to the call for evidence within the context of wider literature and new research.
We do not plan to make representations to the European Commission on the usability and safety of oxo-biodegradable products in the farming industry.
National Park Authority members are selected by constituent local authorities or parish councils or are appointed by the Secretary of State following open competition. All members appointed by the Secretary of State are governed by the Cabinet Office’s Code of Conduct for Board Members of Public Bodies. This sets out the personal and professional standards expected from non-executive board members of UK public bodies and forms part of their terms of appointment. The latest version of the Code of Conduct for Board Members of Public Bodies was published on GOV.UK in June 2019 and can found here: https://www.gov.uk/government/publications/code-of-conduct-for-board-members-of-public-bodies
The aim of speed management is to deliver a balance between safety objectives for all road users and mobility objectives, to ensure efficient travel, as well as environmental and community outcomes. The Department has published guidance designed to make sure that speed limits are appropriately and consistently set while allowing for flexibility to deal with local needs and conditions.
The regulatory emissions tests for type approval of new vehicles are conducted under dynamic rather than constant speeds in order to be more representative of real-world use. The Department does not have specific results for the situations outlined. Transport emission factors are used within the National Atmospheric Emissions Inventory to provide information on the emissions of vehicle fleets based upon factors such as their average speed, fuel type and engine capacity. These are also used within the Emissions Factor Toolkit, published by DEFRA, to assist local authorities carrying out assessment of local air quality.
In January 2022, the median waiting time for admitted ophthalmology patients between referral to treatment was 12.45 weeks. While this includes waiting times for cataract surgery, it does not measure it separately.
The Getting It Right First Time (GIRFT) programme is increasing the adoption of best practice in clinical pathways and supporting high flow cataract surgery to reduce waiting times. GIRFT and the Royal College of Ophthalmologists are advising providers and the National Health Service is increasing capacity through protected elective surgical hubs dedicated to planned procedures. There are currently over 40 elective surgical hubs in England, with further expansion planned in all regions supported by a further £1.5 billion in capital funding. GIRFT is also identifying where trusts with capacity can offer mutual aid to neighbouring providers with longer waiting lists. GIRFT is also supporting partnerships between the NHS and independent sector providers to increase capacity.
There have been no specific discussions on cross-border collaboration for reducing waiting lists for cataract surgery. However, cross border support is already being provided in specialist orthopaedics.
National Health Service organisations should consider the specific facts in a case-by-case basis and in accordance with their local disciplinary policy and procedures. Any investigation should establish whether the staff member intentionally, recklessly, carelessly, or negligently put patients and/or other members of staff at risk of infection. This may result in dismissal as the ultimate sanction.
If any internal investigation identifies a criminal offence has been committed, the employing organisation will need to make a referral to the relevant police force. Any charges of assault would be a matter for the police and Civil Court.
No specific assessment has been made.
The National Institute for Health and Care Excellence’s guidelines describe best practice but are not mandatory, although health and care commissioners are expected to take them fully into account.
No specific assessment has been made.
The National Institute for Health and Care Excellence’s guidelines describe best practice but are not mandatory, although health and care commissioners are expected to take them fully into account.
Public Health England (PHE) is responsible for the central storage and distribution of ultra-low temperature COVID-19 vaccines. In its preparations to receive vaccines, PHE determined the freezer capacity requirement to support the United Kingdom programme during summer 2020 and secured the freezers against that requirement. These were commissioned and in service before arrival of the vaccine. They provide sufficient storage for approximately five million doses of COVID-19 vaccines which require minus 60 degree Celsius storage or below.
From 14 January, six community pharmacies in England started to offer the COVID-19 vaccination service, with an additional 65 pharmacy-led sites joining from the week commencing 21 January. More pharmacies will be stood up over the coming weeks and months.
The Department, NHS England and NHS Improvement and community pharmacy representative bodies will be working together to establish how community pharmacies’ role could be expanded further in the vaccination programme.
As health is a devolved matter, the commissioning of community pharmacies to provide COVD-19 vaccination in Scotland, Wales and Northern Ireland are decisions for the respective devolved administrations.
The Department has not had any discussions or approaches from Warren Medical Limited about the provision of services and supplies related to COVID-19.
The procurement of vials is the responsibility of the manufacturer and the United Kingdom Government has actively engaged with each manufacturer regarding manufacturing capacity, procurement and delivery to ensure enough stock is available, providing additional support where required. The UK has a sufficient number of glass vials available, due to orders already placed with manufacturers.
The Oxford/AstraZeneca vaccine is currently being filled and finished at the Wockhardt site.
The Government has recently extended Wockhardt’s contract from 18 to 24 months to ensure that we have uninterrupted capability into 2022. Specific details of contract fulfillment are commercially sensitive.
Assurances agreed between the Government and Oxford/AstraZeneca are bound by commercially confidential contracts.
NHS England releases weekly vaccination data which shows that as of 15 April:
- 94.2% eligible residents in older adult care homes in England have received at least their first dose of a COVID-19 vaccine;
- 79.4% eligible staff in older adult resident care homes have received at least their first dose; and
- 95.2% of patients over 80 years old have received at least their first dose of a COVID-19 vaccine.
The percentage of National Health Service trust health care workers who have received at least their first dose is not currently available, as NHS England’s data does not currently include all frontline health workers as a sub-group.
COVID-19 vaccination data for Scotland, Wales and Northern Ireland is not collected centrally in the format requested as this is a devolved matter.
The Medicines and Healthcare products Regulatory Agency’s (MHRA’s) Information for Healthcare Professionals regarding the Pfizer vaccine states that a second dose of it should be given at least 21 days after the first dose. For the AstraZeneca vaccine, the Information for Healthcare Professionals states that the second dose should be given between four and 12 weeks after the first dose. This advice is based on clinical trial data and other information submitted to MHRA by the manufacturer.
Based on trial data showing the effectiveness of both vaccines, the Joint Committee on Vaccination and Immunisation (JCVI) advised that both vaccines should be given up to 12 weeks apart. The JCVI also advised that priority should be given to having a greater number of people given a first dose, which would have a greater public health impact than prioritising second doses.
The United Kingdom operates a system of informed consent for vaccinations. When advice from the Joint Committee on Vaccination and Immunisation informed changes to the timings of the secondary dose, general practitioners (GPs) were asked to rebook the appointments. Vaccination centres book in appointments with individuals for both the first and second dose at the same time. Additionally, vaccinations are noted in GP health records and the National Immunisation Management System, which can be accessed by the national booking service to follow up on any missed second doses.
Previous incomplete vaccinations, where the course has been interrupted or delayed, should be resumed using the same vaccination. However, the first dose should not be repeated.
The total length of protection from vaccines against COVID-19 is not yet fully understood. Vaccine developers and manufacturers continue to collect data on the performance of their vaccines. Through their surveillance strategy Public Health England (PHE) continues to assess the effectiveness of vaccines, including duration of protection. A copy of PHE’s COVID-19 vaccine surveillance Strategy is attached.
On 26 January the Joint Committee on Vaccine and Immunisation (JCVI) published an online report, Optimising the COVID-19 vaccination programme for maximum short-term impact. The report found that short-term vaccine efficacy from the first dose of the Pfizer/BioNTech vaccine is calculated at around 90% and from the first dose of the Oxford/ AstraZeneca vaccine is calculated at around 70%, with high protection against severe disease.
Given the high level of protection afforded by the first dose, models suggest that initially vaccinating a greater number of people with a single dose will prevent more deaths and hospitalisations than vaccinating a smaller number of people with two doses. The second dose is important to provide longer lasting protection and is expected to be as or more effective when delivered at an interval of 12 weeks from the first dose. The JCVI has based their advice on the assumption that protection from a first dose of either vaccination will wane in the medium term and that a second dose will offer more long term protection.
Diagnosis of COVID-19 infection has largely been based on reverse transcriptase polymerase chain reaction amplification of viral nucleic acid (RNA) from upper respiratory tract swabs. However, detection of viral RNA has also been reported in blood, serum and plasma from small clinical case series.
The frequency and quantification of RNA in blood fractions and the significance of blood as a transmission route remains unknown.
It is common for viruses to mutate - over 4,000 variants of SARS-CoV-2 have been identified worldwide. The United Kingdom has a world leading surveillance system that supports the detection, analysis and identification of any variants circulating globally which may be of concern.
COVID-19 Genomics UK will continue to lead on monitoring virus samples for new variants. The Department and Public Health England will continue to study the virus closely to understand how it is behaving, where it might have originated from and the spread of the new variant across the UK.
Public Health England monitors the evidence on COVID-19, including articles such as that by Apolone et al.
This published study uses in-house serological methods which require considerable assurance on their specificity and sensitivity, which is not provided in the paper. Therefore, there are several reservations about the laboratory methods used, which provide uncertainty about the conclusions drawn.
Whilst indicative of the possibility, this article is not definitive evidence of the presence of COVID-19 virus in Italy in December and additional supportive evidence is required to achieve high confidence in this assertion.
The United Kingdom has not had any specific discussions with the World Health Organization on the emergence of COVID-19 in France and Italy. The UK Government received notification of France and Italy’s first COVID-19 cases through the European Early Warning and Response System. France reported its first three COVID-19 cases on 24 January 2020. Italy reported its first two COVID-19 cases on 31 January 2020.
The Government has not made any assessment of reports of COVID-19 appearing in wastewater in Barcelona in 2019. In the UK, a national wastewater surveillance programme was announced on 12 June 2020 by the Department of Environment, Food and Rural Affairs, the Scottish and Welsh devolved administrations, focusing on sewage monitoring as part of an advance warning system to detect new outbreaks of COVID-19.
To date the Medicines and Healthcare products Regulatory Agency (MHRA), as well as independent expert advisors on the Commission on Human Medicines and its Expert Working Groups, have completed the assessment of the quality, safety and efficacy data only for the Pfizer/BioNTech vaccine. This vaccine is an mRNA vaccine and data supported a two dose regimen. Efficacy was evaluated in terms of prevention of COVID-19 caused by the SARS-CoV-2 virus, in terms of vulnerability to COVID-19 of the person vaccinated. Clinical trial data showed that, compared to the placebo, efficacy of the Pfizer/BioNTech vaccine from first COVID-19 occurrence from seven days after dose two in participants with or without evidence of prior infection with SARS-CoV-2 was 94.6% - a 95% credible interval of 89.9% to 97.3%).
There is currently no data available regarding transmission of COVID-19 to others in a person who has been vaccinated using any of the COVID-19 vaccines. There is also currently no data available for any COVID-19 vaccine on the period after vaccination for which a person can remain asymptomatic.
To date the Medicines and Healthcare products Regulatory Agency (MHRA), as well as independent expert advisors on the Commission on Human Medicines and its Expert Working Groups, have completed the assessment of the quality, safety and efficacy data only for the Pfizer/BioNTech vaccine. This vaccine is an mRNA vaccine and data supported a two dose regimen. Efficacy was evaluated in terms of prevention of COVID-19 caused by the SARS-CoV-2 virus, in terms of vulnerability to COVID-19 of the person vaccinated. Clinical trial data showed that, compared to the placebo, efficacy of the Pfizer/BioNTech vaccine from first COVID-19 occurrence from seven days after dose two in participants with or without evidence of prior infection with SARS-CoV-2 was 94.6% - a 95% credible interval of 89.9% to 97.3%).
There is currently no data available regarding transmission of COVID-19 to others in a person who has been vaccinated using any of the COVID-19 vaccines. There is also currently no data available for any COVID-19 vaccine on the period after vaccination for which a person can remain asymptomatic.
To date the Medicines and Healthcare products Regulatory Agency (MHRA), as well as independent expert advisors on the Commission on Human Medicines and its Expert Working Groups, have completed the assessment of the quality, safety and efficacy data only for the Pfizer/BioNTech vaccine. This vaccine is an mRNA vaccine and data supported a two dose regimen. Efficacy was evaluated in terms of prevention of COVID-19 caused by the SARS-CoV-2 virus, in terms of vulnerability to COVID-19 of the person vaccinated. Clinical trial data showed that, compared to the placebo, efficacy of the Pfizer/BioNTech vaccine from first COVID-19 occurrence from seven days after dose two in participants with or without evidence of prior infection with SARS-CoV-2 was 94.6% - a 95% credible interval of 89.9% to 97.3%).
There is currently no data available regarding transmission of COVID-19 to others in a person who has been vaccinated using any of the COVID-19 vaccines. There is also currently no data available for any COVID-19 vaccine on the period after vaccination for which a person can remain asymptomatic.
To date the Medicines and Healthcare products Regulatory Agency (MHRA), as well as independent expert advisors on the Commission on Human Medicines and its Expert Working Groups, have completed the assessment of the quality, safety and efficacy data only for the Pfizer/BioNTech vaccine. This vaccine is an mRNA vaccine and data supported a two dose regimen. Efficacy was evaluated in terms of prevention of COVID-19 caused by the SARS-CoV-2 virus, in terms of vulnerability to COVID-19 of the person vaccinated. Clinical trial data showed that, compared to the placebo, efficacy of the Pfizer/BioNTech vaccine from first COVID-19 occurrence from seven days after dose two in participants with or without evidence of prior infection with SARS-CoV-2 was 94.6% - a 95% credible interval of 89.9% to 97.3%).
There is currently no data available regarding transmission of COVID-19 to others in a person who has been vaccinated using any of the COVID-19 vaccines. There is also currently no data available for any COVID-19 vaccine on the period after vaccination for which a person can remain asymptomatic.
The Joint Committee on Vaccination and Immunisation (JCVI) has recommended that as many people on the JCVI’s priority list as possible should be offered a first vaccine dose as the initial priority. One dose of the vaccine offers important protection and allows us to reach as many at risk people as possible in order to offer protection until the second dose can be administered. All individuals will subsequently receive a second dose in due course.
It can be assumed that protection from the first dose will require boosting in order to provide more durable protection. The JCVI supports a two-dose vaccine schedule for the Pfizer-BioNTech and AstraZeneca vaccines.
General practice providers are responsible under the Enhanced Service Specification: COVID-19 vaccination programme 2020/21 for using existing local systems to undertake local call and recall. They use nationally determined text where available, identifying and inviting all eligible patient cohorts on their registered list to book vaccination appointments. Primary Care Network sites will be responsible for checking that all eligible patients have an appointment and recall invitation or re-contacting the patients where they have not. A booking reminder will be sent before each appointment for dose one and dose two of the vaccine.
To date the Medicines and Healthcare products Regulatory Agency (MHRA), as well as independent expert advisors on the Commission on Human Medicines and its Expert Working Groups, have completed the assessment of the quality, safety and efficacy data only for the Pfizer/BioNTech vaccine. This vaccine is an mRNA vaccine and data supported a two dose regimen. Efficacy was evaluated in terms of prevention of COVID-19 caused by the SARS-CoV-2 virus, in terms of vulnerability to COVID-19 of the person vaccinated. Clinical trial data showed that, compared to the placebo, efficacy of the Pfizer/BioNTech vaccine from first COVID-19 occurrence from seven days after dose two in participants with or without evidence of prior infection with SARS-CoV-2 was 94.6% - a 95% credible interval of 89.9% to 97.3%).
There is currently no data available regarding transmission of COVID-19 to others in a person who has been vaccinated using any of the COVID-19 vaccines. There is also currently no data available for any COVID-19 vaccine on the period after vaccination for which a person can remain asymptomatic.
To date the Medicines and Healthcare products Regulatory Agency (MHRA), as well as independent expert advisors on the Commission on Human Medicines and its Expert Working Groups, have completed the assessment of the quality, safety and efficacy data only for the Pfizer/BioNTech vaccine. This vaccine is an mRNA vaccine and data supported a two dose regimen. Efficacy was evaluated in terms of prevention of COVID-19 caused by the SARS-CoV-2 virus, in terms of vulnerability to COVID-19 of the person vaccinated. Clinical trial data showed that, compared to the placebo, efficacy of the Pfizer/BioNTech vaccine from first COVID-19 occurrence from seven days after dose two in participants with or without evidence of prior infection with SARS-CoV-2 was 94.6% - a 95% credible interval of 89.9% to 97.3%).
There is currently no data available regarding transmission of COVID-19 to others in a person who has been vaccinated using any of the COVID-19 vaccines. There is also currently no data available for any COVID-19 vaccine on the period after vaccination for which a person can remain asymptomatic.
To date the Medicines and Healthcare products Regulatory Agency (MHRA), as well as independent expert advisors on the Commission on Human Medicines and its Expert Working Groups, have completed the assessment of the quality, safety and efficacy data only for the Pfizer/BioNTech vaccine. This vaccine is an mRNA vaccine and data supported a two dose regimen. Efficacy was evaluated in terms of prevention of COVID-19 caused by the SARS-CoV-2 virus, in terms of vulnerability to COVID-19 of the person vaccinated. Clinical trial data showed that, compared to the placebo, efficacy of the Pfizer/BioNTech vaccine from first COVID-19 occurrence from seven days after dose two in participants with or without evidence of prior infection with SARS-CoV-2 was 94.6% - a 95% credible interval of 89.9% to 97.3%).
There is currently no data available regarding transmission of COVID-19 to others in a person who has been vaccinated using any of the COVID-19 vaccines. There is also currently no data available for any COVID-19 vaccine on the period after vaccination for which a person can remain asymptomatic.
To date the Medicines and Healthcare products Regulatory Agency (MHRA), as well as independent expert advisors on the Commission on Human Medicines and its Expert Working Groups, have completed the assessment of the quality, safety and efficacy data only for the Pfizer/BioNTech vaccine. This vaccine is an mRNA vaccine and data supported a two dose regimen. Efficacy was evaluated in terms of prevention of COVID-19 caused by the SARS-CoV-2 virus, in terms of vulnerability to COVID-19 of the person vaccinated. Clinical trial data showed that, compared to the placebo, efficacy of the Pfizer/BioNTech vaccine from first COVID-19 occurrence from seven days after dose two in participants with or without evidence of prior infection with SARS-CoV-2 was 94.6% - a 95% credible interval of 89.9% to 97.3%).
There is currently no data available regarding transmission of COVID-19 to others in a person who has been vaccinated using any of the COVID-19 vaccines. There is also currently no data available for any COVID-19 vaccine on the period after vaccination for which a person can remain asymptomatic.
The article Prevalent Eurasian avian-like H1N1 swine influenza virus with 2009 pandemic viral genes facilitating human infection published in Proceedings of the National Academy of Sciences on 29 June 2020 describes a surveillance study of pigs in slaughterhouses and a veterinary hospital in China carried out between 2011 and 2018.
Of the 30,934 samples from 10 different provinces, 165 tested positive for the Eurasian-avian (EA) like H1N1 swine influenza. Of those testing positive, 77 were selected for genetic sequencing, and 29 were identified as having the Genotype 4, described by the authors. The use of a ferret model indicated that the Genotype 4 virus can infect and transmit.
A serological study (analysis of antibodies in the blood) of farm workers on 15 farms over the period of the study, suggests that approximately 10-12% of farm workers had detectable, specific antibody to G4 H1N1 viruses, indicative of previous infection. The publication is not clear if these were farms that were directly related to the surveillance programme. It would also not be possible to determine when these infections occurred.
The New and Emerging Respiratory Virus Threats Advisory Group is reviewing the risk associated with the genotype 4 (G4) reassortant Eurasian avian-like (EA) H1N1 virus, described in this publication.
We continually assess the most significant threats that the United Kingdom and its citizens could face, including natural hazard risks such as a pandemic influenza.
The Government continues to review and improve surveillance for potentially zoonotic and new and emerging infections, with early detection through horizon scanning and epidemic intelligence activities, research, and continually improving diagnostic techniques for the identification of zoonotic pathogens.
In line with our standard practice, Public Health England is undertaking a risk assessment of the G4 influenza virus and we will take any appropriate action based on robust scientific and clinical advice.
R is estimated by a number of independent modelling groups based at universities and Public Health England. Evidence from the different models is considered, discussed, combined, and then a consensus estimate is presented to the Scientific Advisory Group for Emergencies as a range.
Individual modelling groups use a variety of different data sources to estimate R. This includes epidemiological data such as the number of hospital admissions and deaths, and surveys that gather information on the behaviour of individuals. The models include assumptions about numbers of individuals who require no health service intervention which are informed by a range of studies including household infection surveys.
The Government is building up United Kingdom manufacturing with signed contracts to manufacture over two billion items of personal protective equipment (PPE) through UK-based manufacturers, including facemasks, visors, gowns and aprons.
Lord Deighton is leading the Government effort by British industry to manufacture PPE. The Government is currently in contact with over 350 potential UK manufacturers, and engineering efforts by small companies are being scaled up. We have already taken delivery of products from new, certified UK manufacturers. More new manufacturers of PPE are expected to commit to producing PPE in the coming weeks, with 25 opportunist companies in final commercial discussions.
To provide a more comprehensive response to a number of outstanding Written Questions, this has been answered by an information factsheet Testing – note for House of Lords which is attached, due to the size of the data. A copy has also been placed in the Library
The Senior Deputy Speaker has asked me, as Chair of the Services Committee, to respond on his behalf. Trimble Space Scheduling (TSS), formally Trimble Manhattan Space Scheduling, provide the room bookings software which is used by the House of Lords Attendants’ Office to co-ordinate the bookings of committee rooms and meeting rooms. The software is provided under a contract between the Corporate Officer of the House of Lords and the Corporate Officer of the House of Commons, and Trimble Space Scheduling. The Parliamentary Digital Service has day-to-day responsibility for oversight of arrangements under the contract.
We are in regular dialogue with our European partners and stand ready to provide humanitarian assistance as needed. Total UK aid to Ukraine and the region for the current crisis comes to almost £400 million. This includes £220 million of humanitarian assistance and £100 million to bolster the Ukrainian economy and reduce Ukraine's reliance on Russian gas imports.
Our humanitarian support will help partners stand up their response to the deteriorating humanitarian situation, and create a lifeline for Ukrainians with access to basic necessities. We have also deployed UK humanitarian experts to support Ukraine's neighbours, who are receiving and supporting the increasing flow of refugees fleeing Ukraine.
During the 1990 discussions on German reunification, no written assurances about the further enlargement of NATO beyond Germany were made to Mr Gorbachev or other representatives of the Government of the Soviet Union. Despite consistent assertion, Russian leaders have been unable to produce any written evidence that such assurances were made.
We are committed to introducing new legislation to ensure our security services and law enforcement agencies have the tools they need to disrupt state threats.
The Government is reviewing responses to the Public Consultation on legislative proposals to tackle state threats which concluded last year. Legislation will be introduced as soon as parliamentary time allows
Self-isolation is a vitally important weapon in the battle against the spread of the virus, it ensures that friends, family, community, and NHS are protected. Therefore, a new legal duty was introduced in September 2020 requiring a person in England to self-isolate for 10 days if they tested positive for the COVID-19.
To increase compliance and ensure our domestic self-isolation regime is effective failure to self-isolate can result in an FPN of £1000 for the first offence. This increases to £2000 for a second offence, £4000 for a third offence and £10,000 for a fourth and any subsequent offence. Failure to pay a Domestic Self-Isolation Fixed Penalty Notice can be subject to criminal proceedings.
There may be some circumstances where someone could be charged with assault by risking harm to others in passing on COVID-19 but such charging decisions would be for the Crown Prosecution Service to consider.
Since the EU Settlement Scheme (EUSS) opened in March 2019, the Home Office has undertaken a broad range of communications and stakeholder engagement activity to encourage EU, European Economic Area (EEA) and European Free Trade Association (EFTA) nationals, and their family members, to apply for status under the EUSS and to explain why they should do so and secure their rights under the Citizens’ Rights Agreements.
We launched a further wave of UK-wide advertising in mid-May to help ensure they were aware of the EUSS and its benefits and of how to apply and access support in doing so if they needed it, although existing ILR holders need not apply. This built on the successful campaign already delivered – with £7.9 million having now been invested in such activity – with targeted adverts appearing on social media, website banners, catch up TV and radio up to the application deadline of 30 June.
The Home Office has also made available £22 million in grant funding for a network of now 72 organisations across the UK, which includes charities, local authorities and community groups, to engage with vulnerable groups and help them apply to the EUSS.
We are also continuing to engage with local authorities, the Devolved Administrations, employers, community groups and others to raise awareness of the EUSS and encourage those eligible who are yet to apply to do so.
Since the EU Settlement Scheme (EUSS) opened in March 2019, the Home Office has undertaken a broad range of communications and stakeholder engagement activity to encourage EU, European Economic Area (EEA) and European Free Trade Association (EFTA) nationals, and their family members, to apply for status under the EUSS and to explain why they should do so and secure their rights under the Citizens’ Rights Agreements.
We launched a further wave of UK-wide advertising in mid-May to help ensure they were aware of the EUSS and its benefits and of how to apply and access support in doing so if they needed it, although existing ILR holders need not apply. This built on the successful campaign already delivered – with £7.9 million having now been invested in such activity – with targeted adverts appearing on social media, website banners, catch up TV and radio up to the application deadline of 30 June.
The Home Office has also made available £22 million in grant funding for a network of now 72 organisations across the UK, which includes charities, local authorities and community groups, to engage with vulnerable groups and help them apply to the EUSS.
We are also continuing to engage with local authorities, the Devolved Administrations, employers, community groups and others to raise awareness of the EUSS and encourage those eligible who are yet to apply to do so.
A person who is issued with a UK Immigration status or Indefinite leave to Enter or Remain are provided with a visa in their passport, a biometric residence permit or an electronic visa confirming their status. Our decision notices also provide customers with details on their terms of leave.
A person who has applied to the EU Settlement Scheme or via the fully digital processes for the British Nationals (Overseas) and Points Based System routes, will have created a UK Visas and Immigration (UKVI) account. They can use their UKVI account credentials to log into the online View and Prove service.
If an individual has been notified they have a digital certificate of application, they are able to use the View and Prove service to prove their rights:
https://www.gov.uk/view-prove-immigration-status
The Home Office also publishes information to assist EU national customers understand their immigration status. Further information can be found on our website: https://www.gov.uk/government/publications/view-and-prove-your-immigration-status-evisa/your-immigration-status-an-introduction-for-eu-eea-and-swiss-citizens-accessible-version
For longer-term settled residents who wish to replace their visa for a biometric residence permit, they can submit an application for a biometric residence permit. Further information can be found on the gov.uk website: https://www.gov.uk/biometric-residence-permits/replace-visa-brp
An EU, European Economic Area (EEA) or European Free Trade Association (EFTA) national who was settled in the UK before 1 January 1973 may have acquired indefinite leave to enter or remain automatically under section 1(2) of the Immigration Act 1971.
Where they hold indefinite leave to enter or remain obtained in this way, or where an EU, EEA or EFTA national holds such leave obtained by applying for it under another immigration route, they do not need to apply for status under the EU Settlement Scheme (EUSS), but they may do so if they wish given the benefits of doing so.
Indefinite leave to enter or remain granted under the EUSS (referred to as ‘settled status’) enables the holder to access additional rights in line with the Citizens’ Rights Agreements. For example, they can be absent from the UK for five consecutive years, rather than two years, before their settled status lapses, and they can sponsor certain family members to join them in the UK without meeting the requirements of the family Immigration Rules.
Where an EEA national was resident in the UK by 31 December 2020 based on free movement rights, they must apply to the EU Settlement Scheme for status under UK immigration law. The deadline for doing so was 30 June 2021, but late applications will be accepted where reasonable grounds exist for missing the deadline. This includes where someone has lived in the UK for many years and did not realise they needed to apply.
An EU, European Economic Area (EEA) or European Free Trade Association (EFTA) national who was settled in the UK before 1 January 1973 may have acquired indefinite leave to enter or remain automatically under section 1(2) of the Immigration Act 1971.
Where they hold indefinite leave to enter or remain obtained in this way, or where an EU, EEA or EFTA national holds such leave obtained by applying for it under another immigration route, they do not need to apply for status under the EU Settlement Scheme (EUSS), but they may do so if they wish given the benefits of doing so.
Indefinite leave to enter or remain granted under the EUSS (referred to as ‘settled status’) enables the holder to access additional rights in line with the Citizens’ Rights Agreements. For example, they can be absent from the UK for five consecutive years, rather than two years, before their settled status lapses, and they can sponsor certain family members to join them in the UK without meeting the requirements of the family Immigration Rules.
Where an EEA national was resident in the UK by 31 December 2020 based on free movement rights, they must apply to the EU Settlement Scheme for status under UK immigration law. The deadline for doing so was 30 June 2021, but late applications will be accepted where reasonable grounds exist for missing the deadline. This includes where someone has lived in the UK for many years and did not realise they needed to apply.
EU, European Economic Area (EEA) and European Free Trade Association (EFTA) nationals now require UK immigration status to live in the UK. Where they do not already hold such status, they may obtain it under the EU Settlement Scheme (EUSS), where they were resident in the UK by 31 December 2020 or are a family member joining such a person, or under the points-based immigration system.
EU, EEA and EFTA nationals who acquired a right of permanent residence here under EU law still need to apply for status under the EUSS.
Those who already have indefinite leave to enter or remain in the UK do not need to apply for EUSS status, but may do so, free of charge, if they wish, to take advantage of the additional rights available to them under the Citizens’ Rights Agreements.
EU, European Economic Area (EEA) and European Free Trade Association (EFTA) nationals now require UK immigration status to live in the UK. Where they do not already hold such status, they may obtain it under the EU Settlement Scheme (EUSS), where they were resident in the UK by 31 December 2020 or are a family member joining such a person, or under the points-based immigration system.
EU, EEA and EFTA nationals who acquired a right of permanent residence here under EU law still need to apply for status under the EUSS.
Those who already have indefinite leave to enter or remain in the UK do not need to apply for EUSS status, but may do so, free of charge, if they wish, to take advantage of the additional rights available to them under the Citizens’ Rights Agreements.
The Home Office previously engaged with the French on this issue of the applicability of French maritime regulation to migrant vessels and will continue to do so. However, any decision on when, where and how to apply French law in this area must be a matter for the French, in their jurisdiction.
Our New Plan for Immigration and the legislation to implement it will bring root and branch reform to the asylum system. We will take tougher action against anyone who facilitates illegal entry, such as by piloting a small boat. We plan to increase the maximum sentence for people smuggling to life imprisonment.
Border Force will be granted additional powers to stop illegal migration, including the ability to stop and redirect vessels at sea. These reforms will break the business model of criminal trafficking networks. They will deter illegal entry into this country and make it unviable.
The Home Office did reply to Mr Sharrod’s letters of 13 August 2020 and 20 October 2020, which was raised with the Home Office by a member in another place.
The Home Office previously engaged with the French on this issue of the applicability of French maritime regulation to migrant vessels and will continue to do so. However, any decision on when, where and how to apply French law in this area must be a matter for the French, in their jurisdiction. The Home Office is aware of France's obligations under the Migrant Smuggling Protocol to prevent illegal migration.
Our New Plan for Immigration and the legislation to implement it will bring root and branch reform to the asylum system. We will take tougher action against anyone who facilitates illegal entry, such as by piloting a small boat. We plan to increase the maximum sentence for people smuggling to life imprisonment.
Border Force will be granted additional powers to stop illegal migration, including the ability to stop and redirect vessels at sea. These reforms will break the business model of criminal trafficking networks. They will deter illegal entry into this country and make it unviable.
The Home Office did reply to Mr Sharrod’s letters of 13 August 2020 and 20 October 2020, which was raised with the Home Office by a member in another place.
The Home Office previously engaged with the French on this issue of the applicability of French maritime regulation to migrant vessels and will continue to do so. However, any decision on when, where and how to apply French law in this area must be a matter for the French, in their jurisdiction. The Home Office is aware of France's obligations under the Migrant Smuggling Protocol to prevent illegal migration.
Our New Plan for Immigration and the legislation to implement it will bring root and branch reform to the asylum system. We will take tougher action against anyone who facilitates illegal entry, such as by piloting a small boat. We plan to increase the maximum sentence for people smuggling to life imprisonment.
Border Force will be granted additional powers to stop illegal migration, including the ability to stop and redirect vessels at sea. These reforms will break the business model of criminal trafficking networks. They will deter illegal entry into this country and make it unviable.
The Home Office did reply to Mr Sharrod’s letters of 13 August 2020 and 20 October 2020, which was raised with the Home Office by a member in another place.
The Home Office previously engaged with the French on this issue of the applicability of French maritime regulation to migrant vessels and will continue to do so. However, any decision on when, where and how to apply French law in this area must be a matter for the French, in their jurisdiction. The Home Office is aware of France's obligations under the Migrant Smuggling Protocol to prevent illegal migration.
Our New Plan for Immigration and the legislation to implement it will bring root and branch reform to the asylum system. We will take tougher action against anyone who facilitates illegal entry, such as by piloting a small boat. We plan to increase the maximum sentence for people smuggling to life imprisonment.
Border Force will be granted additional powers to stop illegal migration, including the ability to stop and redirect vessels at sea. These reforms will break the business model of criminal trafficking networks. They will deter illegal entry into this country and make it unviable.
Officials have been pursuing work on several fronts to improve our understanding of the characteristics of group-based child sexual exploitation, as well as the implications for the investigation and prevention of these crimes.
This internal work is being carried out as part of routine policy development. As such, it has not been undertaken with the intention of publication.
Much of the insight gained through our work with law enforcement partners contains operationally and personally sensitive information and will need to remain confidential.
In early 2020 the Government will publish a national strategy, the first of its kind, to tackle all forms of child sexual abuse.
Our new strategy will set out our whole system response to tackling child sexual abuse, including group-based sexual offending, drawing on this internal work. It will set out how we will work across government, law enforcement, safeguarding partners and industry to root out offending, protect victims and help victims and survivors rebuild their lives. We will work tirelessly to tackle all forms of sexual abuse; there will be no no-go areas.
The UK has some of the toughest powers in the world to deal with sex offenders and we are committed to ensuring that the system is as robust as it can be.
Registered sex offenders are managed by the police, who assess the risk each individual poses to the public and monitor changes to offenders’ circumstances.
Offenders must tell the police any names that they have used, including ones used online, and must notify the police within 3 days of any name change. This includes notifying the police of any changes to the offender’s passport or other identity documents. A failure to inform the police of a change in name constitutes a breach of notification requirements which is a criminal offence carrying up to 5 years’ imprisonment.
We will continue to work with the police to ensure they have all the necessary tools to manage sex offenders effectively.
The Home Office does not hold information centrally on the number of custody suites across England and Wales.
Decisions on the use of resources, including custody suites, are a matter for Police and Crime Commissioners and Chief Constables as they best understand the needs of the communities they serve.
Decisions on calling in applications are made in line with published call-in policy as set out in a Written Ministerial Statement by Nick Boles on 26 October 2012. The policy makes it clear that the power to call in a case will only be used very selectively. Air pollution levels are a potential consideration when considering whether to call in an application.
In December 2016, the Secretary of State declined to call in this application for his own determination. Following the categorisation of Canterbury as an air quality management area, he received requests to reconsider that decision. These requests were carefully considered having regard to his policy on calling in planning applications. The Secretary of State decided that his original decision, not to call in this application, should stand, and that the application should remain to be determined by the local planning authority.
Decisions on calling in applications are made in line with published call-in policy as set out in a Written Ministerial Statement by Nick Boles on 26 October 2012. The policy makes it clear that the power to call in a case will only be used very selectively. Air pollution levels are a potential consideration when considering whether to call in an application.
The Local Government Act 1972 allows local planning authorities (including National Parks) to arrange for the discharge of any of its functions by a committee, sub-committee, or an officer. The operation of such committees, including which applications are considered by members and the procedure by which they are governed, are administrative matters for the National Park Authority.
Like other planning committees, where a decision is made by a National Park planning committee, members should carefully consider all the evidence before them and must be prepared to modify or change their initial view in light of the arguments and evidence presented to them. They must make their final decision at the meeting with an open mind based on this evidence. The law requires that planning decisions are made in accordance with the local development plan, unless material considerations indicate otherwise.
National Park authorities must also promote and maintain high standards of conduct by their members. Members have to abide by their authorities’ code of conduct and this must be consistent with the seven ‘Nolan’ principles of standards in public life. National Park Authorities are responsible for ensuring members observe their codes of conduct and maintain high standards.
The Local Government Act 1972 allows local planning authorities (including National Parks) to arrange for the discharge of any of its functions by a committee, sub-committee, or an officer. The operation of such committees, including which applications are considered by members and the procedure by which they are governed, are administrative matters for the National Park Authority.
Like other planning committees, where a decision is made by a National Park planning committee, members should carefully consider all the evidence before them and must be prepared to modify or change their initial view in light of the arguments and evidence presented to them. They must make their final decision at the meeting with an open mind based on this evidence. The law requires that planning decisions are made in accordance with the local development plan, unless material considerations indicate otherwise.
National Park authorities must also promote and maintain high standards of conduct by their members. Members have to abide by their authorities’ code of conduct and this must be consistent with the seven ‘Nolan’ principles of standards in public life. National Park Authorities are responsible for ensuring members observe their codes of conduct and maintain high standards.
There are two settings in which a child aged 16 or under may be handcuffed: through interaction with the Police, or within a secure setting overseen by the Youth Custody Service.
Owing to the way in which police use of force data is collected, data is recorded on the number of times a tactic was used, not the number of unique events or people involved in incidents. 36,279 police handcuffing tactics were recorded for those aged under 18 in the year ending March 2020.
In 2019/20, in Young Offender Institutions and Secure Training Centres handcuffs were applied to children under the age of 16 on 117 occasions, involving 63 different individual children.
Any use of force, including the use of handcuffs by the Police or within a secure setting, must be reasonable and necessary in the circumstances, proportionate to the threat posed and only the minimum force necessary may be used.
The College of Policing is responsible for setting the standards and training to which police operate. Guidance on the use of force and restraint by the police is set out in the College of Policing Authorised Professional Practice, which includes guidance on how to deal with vulnerable people.
In Young Offender Institutions and Secure Training Centres, handcuffs are one of a range of approved restraint techniques. Handcuffs are used as an ethical and safer alternative to physical restraint technique. The use of handcuffs must always be reasonable and proportionate, and with the aim of preventing harm occurring to the young person or others. A report must be made every time handcuffs are used.
There are two settings in which a child aged 16 or under may be handcuffed: through interaction with the Police, or within a secure setting overseen by the Youth Custody Service.
Owing to the way in which police use of force data is collected, data is recorded on the number of times a tactic was used, not the number of unique events or people involved in incidents. 36,279 police handcuffing tactics were recorded for those aged under 18 in the year ending March 2020.
In 2019/20, in Young Offender Institutions and Secure Training Centres handcuffs were applied to children under the age of 16 on 117 occasions, involving 63 different individual children.
Any use of force, including the use of handcuffs by the Police or within a secure setting, must be reasonable and necessary in the circumstances, proportionate to the threat posed and only the minimum force necessary may be used.
The College of Policing is responsible for setting the standards and training to which police operate. Guidance on the use of force and restraint by the police is set out in the College of Policing Authorised Professional Practice, which includes guidance on how to deal with vulnerable people.
In Young Offender Institutions and Secure Training Centres, handcuffs are one of a range of approved restraint techniques. Handcuffs are used as an ethical and safer alternative to physical restraint technique. The use of handcuffs must always be reasonable and proportionate, and with the aim of preventing harm occurring to the young person or others. A report must be made every time handcuffs are used.