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731066
registered interest false more like this
date less than 2017-06-21more like thismore than 2017-06-21
answering body
Department of Health remove filter
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 NHS: Drugs more like this
house id 2 more like this
legislature
25277
pref label House of Lords more like this
question text Her Majesty's Government whether they plan to convert EU Regulation 658/2014 into UK law; and, if so, which UK body will assume the role of the European Medicines Agency for the setting and charging of fees to UK-based marketing authorisation holders. more like this
tabling member printed
Baroness Hayter of Kentish Town more like this
uin HL74 remove filter
answer
answer
is ministerial correction false more like this
date of answer less than 2017-06-29more like thismore than 2017-06-29
answer text <p>The Medicines and Healthcare products Regulatory Agency sets and charges fees for marketing authorisations in the United Kingdom which are granted nationally and not approved centrally by the European Medicines Agency. The extent to which European Medicines Agency procedures will apply in the UK after we have exited the European Union will be subject to negotiations. The Government will ensure that the UK’s full approval regime is ready and operational as soon as the UK has formally departed the EU.</p> more like this
answering member printed Lord O'Shaughnessy more like this
question first answered
less than 2017-06-29T11:37:19.147Zmore like thismore than 2017-06-29T11:37:19.147Z
answering member
4545
label Biography information for Lord O'Shaughnessy more like this
tabling member
4159
label Biography information for Baroness Hayter of Kentish Town more like this