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1146644
registered interest false more like this
date less than 2019-09-26more like thismore than 2019-09-26
answering body
Department for Transport more like this
answering dept id 27 more like this
answering dept short name Transport more like this
answering dept sort name Transport more like this
hansard heading Roads: Suffolk 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 Transport, what discussions his Department has had with Suffolk county council on the Ipswich northern route since 1 January 2019. more like this
tabling member constituency Ipswich more like this
tabling member printed
Sandy Martin more like this
uin 291481 more like this
answer
answer
is ministerial correction true more like this
date of answer less than 2019-10-01more like thismore than 2019-10-01
answer text <p><del class="ministerial">Since 1 January 2019, the Department has liaised with Suffolk County Council to support them in developing the evidence required to facilitate a thorough and efficient assessment of the proposed scheme. This has included analytical support to scheme promoters, in advance of Transport East submitting the scheme proposal to the Department on the County Council’s behalf in July 2019, and following this submission.</del></p><p><ins class="ministerial">Department for Transport officials have had regular discussions with Suffolk County Council regarding the Ipswich Northern Route since January 1 2019. As well as regular engagement, the Department has offered analytical support to all scheme promoters as part of the Major Road Network (MRN) and Large Local Majors (LLM) programme.</ins></p><p> </p><p> </p> more like this
answering member constituency Mid Norfolk remove filter
answering member printed George Freeman more like this
question first answered
less than 2019-10-01T16:04:51.793Zmore like thismore than 2019-10-01T16:04:51.793Z
question first ministerially corrected
less than 2019-10-08T13:22:47.04Zmore like thismore than 2019-10-08T13:22:47.04Z
answering member
4020
label Biography information for George Freeman more like this
previous answer version
136591
answering member constituency Mid Norfolk more like this
answering member printed George Freeman more like this
answering member
4020
label Biography information for George Freeman more like this
tabling member
4678
label Biography information for Sandy Martin more like this
522126
registered interest false more like this
date less than 2016-05-26more like thismore than 2016-05-26
answering body
Department of Health more like this
answering dept id 17 more like this
answering dept short name Health more like this
answering dept sort name Health more like this
hansard heading Human Papillomavirus: Vaccination 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, whether the Medicines and Healthcare Products Regulatory Agency holds any clinical trial data for HPV vaccines which is not in the public domain. more like this
tabling member constituency Denton and Reddish more like this
tabling member printed
Andrew Gwynne more like this
uin 38833 more like this
answer
answer
is ministerial correction true more like this
date of answer less than 2016-06-07more like thismore than 2016-06-07
answer text <p>There are <del class="ministerial">two</del> <ins class="ministerial">three </ins>human papilloma virus vaccines licensed in the European Union: Cervarix<ins class="ministerial">,</ins> <del class="ministerial">and</del> <ins class="ministerial">Gardasil and </ins>Gardasil 9. These products are licensed centrally throughout Europe by the European Commission via the European Medicines Agency (EMA). Applicants for centrally authorised products are required to submit all relevant supporting clinical trials data, whether published or not, to the EMA directly and not to the Medicines and Healthcare products Regulatory Agency.</p><p> </p><p>Under current medicines legislation, the EMA database registers all EU-approved clinical trials of investigational medicinal products. Since March 2011 this information has been publicly accessible through the EU Clinical Trials Register (except adult Phase 1 trials). The EU Clinical Trials Register includes all EU-conducted trials since May 2004 when the Clinical Trials Directive was implemented and can be found here:</p><p> </p><p><a href="https://www.clinicaltrialsregister.eu/ctr-search/search" target="_blank">https://www.clinicaltrialsregister.eu/ctr-search/search</a></p><p> </p><p>Furthermore since July 2014 clinical trial sponsors have been required to provide a summary of their trial results uploaded onto the EU Clinical Trials Register within one year of their trial completing. There is a two year programme of back-loading underway to provide summaries of trial results for all trials on the Register back to when the EudraCT database was initiated in May 2004.</p>
answering member constituency Mid Norfolk remove filter
answering member printed George Freeman more like this
question first answered
less than 2016-06-07T10:57:37.313Zmore like thisremove minimum value filter
question first ministerially corrected
less than 2016-06-13T10:14:27.603Zmore like thismore than 2016-06-13T10:14:27.603Z
answering member
4020
label Biography information for George Freeman more like this
previous answer version
2228
answering member constituency Mid Norfolk more like this
answering member printed George Freeman more like this
answering member
4020
label Biography information for George Freeman more like this
tabling member
1506
label Biography information for Andrew Gwynne more like this