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1022956
registered interest false more like this
date less than 2018-12-10more like thismore than 2018-12-10
answering body
Department for Education more like this
answering dept id 60 more like this
answering dept short name Education more like this
answering dept sort name Education more like this
hansard heading Children: Social Services more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Education, what recent assessment he has made of the correlation between deprivation and demand for children’s services. more like this
tabling member constituency Newcastle-under-Lyme more like this
tabling member printed
Paul Farrelly remove filter
uin 200581 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2018-12-13more like thismore than 2018-12-13
answer text <p>Demand for children’s services is associated with a number of factors, including deprivation. The most deprived local authorities (LAs) have more looked after children (per 10,000 17 year olds), and these rates have grown faster than the least deprived LAs.</p><p>In preparation for the Spending Review, to help ensure decisions are based on the best available evidence, the government is working with the sector to develop a sharper and more granular picture of demand for children’s services.</p><p>We are also working with Ministry of Housing, Communities and Local Government as part of the Government’s Fair Funding Review of relative needs and resources, where new, up-to-date formulas are being developed to ensure funding distribution to councils is based on the best available evidence.</p><p>We welcome the contributions from the sector in this area, including Newton Europe’s Making Sense (2018) report and the Association of Directors of Children’s Services' continuing research reports, Safeguarding Pressures (2018).</p>
answering member constituency Stratford-on-Avon more like this
answering member printed Nadhim Zahawi more like this
question first answered
less than 2018-12-13T14:41:48.833Zmore like thismore than 2018-12-13T14:41:48.833Z
answering member
4113
label Biography information for Nadhim Zahawi more like this
tabling member
1436
label Biography information for Paul Farrelly more like this
1020404
registered interest false more like this
date less than 2018-12-05more like thismore than 2018-12-05
answering body
Department of Health and Social Care more like this
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care more like this
hansard heading Medicines and Healthcare products Regulatory Agency more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Health and Social Care, pursuant to the Answer of 03 December 2018 to Question 196736 on Medicines and Healthcare Products Regulatory Agency (MHRA), and with reference to the transition period set out in the Agreement on the Withdrawal of the United Kingdom of Great Britain and Northern Ireland from the European Union, if the MHRA will be recognised as an EU competent authority under the EU (a) Medical Devices Directive, (b) in-vitro diagnostic medical devices, and (c) Medical Devices Regulation during the period covered by the Agreement. more like this
tabling member constituency Newcastle-under-Lyme more like this
tabling member printed
Paul Farrelly remove filter
uin 199325 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2018-12-10more like thismore than 2018-12-10
answer text <p>The agreement of an implementation period will mean that the Medicines and Healthcare products Regulatory Agency (MHRA) will continue to be recognised as a European Union competent authority designated under the EU Directives for medical devices, in vitro diagnostic medical devices and active implantable medical devices, during this period.</p><p> </p><p>This is also the case for the new EU Regulations for medical devices and in vitro diagnostic medical devices, which both entered into force in May 2017.</p><p> </p><p>It is possible for a single organisation to have individual notified bodies designated in more than one Member State. The authority within each Member State is responsible for notified bodies based in its own country.</p><p> </p><p>The MHRA is responsible for the designation and monitoring of notified bodies in the United Kingdom, which the response to Question 196736 refers to.</p> more like this
answering member constituency Thurrock more like this
answering member printed Jackie Doyle-Price more like this
grouped question UIN 199327 more like this
question first answered
less than 2018-12-10T14:12:25.46Zmore like thismore than 2018-12-10T14:12:25.46Z
answering member
4065
label Biography information for Dame Jackie Doyle-Price more like this
tabling member
1436
label Biography information for Paul Farrelly more like this
1020405
registered interest false more like this
date less than 2018-12-05more like thismore than 2018-12-05
answering body
Department for Exiting the European Union more like this
answering dept id 203 more like this
answering dept short name Exiting the European Union more like this
answering dept sort name Exiting the European Union more like this
hansard heading Medicines and Healthcare products Regulatory Agency more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Exiting the European Union, pursuant to the Answer of 03 December 2018 to Question 196736 on Medicines and Healthcare Products Regulatory Agency (MHRA) and with reference to the transition period set out in the Agreement on the Withdrawal of the United Kingdom of Great Britain and Northern Ireland from the European Union, if the MHRA will be recognised as an EU competent authority under EU Regulations (a) Medical Devices Directive, (b) in-vitro diagnostic medical devices, and (c) Medical Devices Regulation during that period. more like this
tabling member constituency Newcastle-under-Lyme more like this
tabling member printed
Paul Farrelly remove filter
uin 199326 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2018-12-10more like thismore than 2018-12-10
answer text <p>The agreement of an implementation period will mean that the Medicines and Healthcare products Regulatory Agency (MHRA) will continue to be recognised as an EU competent authority designated under the EU Directives for medical devices, in vitro diagnostic medical devices and active implantable medical devices, during this period.</p><p>This is also the case for the new EU Regulations for medical devices and in vitro diagnostic medical devices, which both entered into force in May 2017.</p><p><strong></strong><br><br></p><p> </p> more like this
answering member constituency Daventry more like this
answering member printed Chris Heaton-Harris more like this
question first answered
less than 2018-12-10T15:48:34.12Zmore like thismore than 2018-12-10T15:48:34.12Z
answering member
3977
label Biography information for Chris Heaton-Harris more like this
tabling member
1436
label Biography information for Paul Farrelly more like this
1020408
registered interest false more like this
date less than 2018-12-05more like thismore than 2018-12-05
answering body
Department of Health and Social Care more like this
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care more like this
hansard heading Medical Equipment: UK Notified Bodies more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Health and Social Care, pursuant to the Answer of 03 December 2018 to Question 196736 on Medicines and Healthcare Products Regulatory Agency (MHRA), whether the Department's response refers to (a) UK notified bodies licensed by the MHRA and (b) UK notified bodies that have also secured notified body status in other EU states. more like this
tabling member constituency Newcastle-under-Lyme more like this
tabling member printed
Paul Farrelly remove filter
uin 199327 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2018-12-10more like thismore than 2018-12-10
answer text <p>The agreement of an implementation period will mean that the Medicines and Healthcare products Regulatory Agency (MHRA) will continue to be recognised as a European Union competent authority designated under the EU Directives for medical devices, in vitro diagnostic medical devices and active implantable medical devices, during this period.</p><p> </p><p>This is also the case for the new EU Regulations for medical devices and in vitro diagnostic medical devices, which both entered into force in May 2017.</p><p> </p><p>It is possible for a single organisation to have individual notified bodies designated in more than one Member State. The authority within each Member State is responsible for notified bodies based in its own country.</p><p> </p><p>The MHRA is responsible for the designation and monitoring of notified bodies in the United Kingdom, which the response to Question 196736 refers to.</p> more like this
answering member constituency Thurrock more like this
answering member printed Jackie Doyle-Price more like this
grouped question UIN 199325 more like this
question first answered
less than 2018-12-10T14:12:25.523Zmore like thismore than 2018-12-10T14:12:25.523Z
answering member
4065
label Biography information for Dame Jackie Doyle-Price more like this
tabling member
1436
label Biography information for Paul Farrelly more like this
1016320
registered interest false more like this
date less than 2018-11-28more like thismore than 2018-11-28
answering body
Department of Health and Social Care more like this
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care more like this
hansard heading Medicines and Healthcare products Regulatory Agency more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Health and Social Care, with reference to the transition period set out in the agreement on the withdrawal of the United Kingdom of Great Britain and Northern Ireland from the European Union, whether the Medicines and Healthcare Products Regulatory Agency will retain its status as a competent authority; and whether existing CE marks assigned under that agency will be valid from 29 March 2019 until the end of that transition period. more like this
tabling member constituency Newcastle-under-Lyme more like this
tabling member printed
Paul Farrelly remove filter
uin 196736 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2018-12-03more like thismore than 2018-12-03
answer text <p>The agreement of an implementation period will ensure that access to medicines and medical devices continues, and patient safety is maintained, in both the United Kingdom and European Union markets.</p><p> </p><p>The Medicines and Healthcare products Regulatory Agency (MHRA) will continue to be the UK competent authority during this period.</p><p> </p><p>For medical devices, CE marks are assigned by notified bodies (rather than competent authorities such as the MHRA), and during the implementation period UK notified bodies will continue to conduct third-party conformity assessment in the UK, and the results of these tests will continue to be used and recognised for both the UK and EU markets.</p> more like this
answering member constituency Thurrock more like this
answering member printed Jackie Doyle-Price more like this
question first answered
less than 2018-12-03T18:29:34.66Zmore like thismore than 2018-12-03T18:29:34.66Z
answering member
4065
label Biography information for Dame Jackie Doyle-Price more like this
tabling member
1436
label Biography information for Paul Farrelly more like this
1012294
registered interest false more like this
date less than 2018-11-22more like thismore than 2018-11-22
answering body
Department for Digital, Culture, Media and Sport more like this
answering dept id 10 more like this
answering dept short name Digital, Culture, Media and Sport more like this
answering dept sort name Digital, Culture, Media and Sport more like this
hansard heading Arts: EU Grants and Loans more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Digital, Culture, Media and Sport, whether the Government plans to remain part of Creative Europe after the current funding period concludes in 2020. more like this
tabling member constituency Newcastle-under-Lyme more like this
tabling member printed
Paul Farrelly remove filter
uin 194605 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2018-11-27more like thismore than 2018-11-27
answer text The UK will always be a European country that advocates for cultural diversity as part of its global identity and is committed to continuing its contribution to and support of European culture. The Government has been clear that will be explore participation in any successor programme to Creative Europe. Where EU funding programmes are to the UK and EU's joint advantage, we want to discuss continued participation as part of the negotiations. Ultimately, the decision on which programmes are in the UK’s interests will be decided as part of the future partnership negotiations, which are ongoing. more like this
answering member constituency Stourbridge more like this
answering member printed Margot James more like this
question first answered
less than 2018-11-27T19:18:35.98Zmore like thismore than 2018-11-27T19:18:35.98Z
answering member
4115
label Biography information for Margot James more like this
tabling member
1436
label Biography information for Paul Farrelly more like this