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tabling member printed	Paul Farrelly
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.
max answer › question first answered	2019-05-21T13:17:05.177Z
max answer › date of answer	2018-12-03

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registered interest

date

exactly:

or between:
and

answering body

answering dept id

answering dept short name

answering dept sort name

hansard heading

house id

legislature


pref label

question text

tabling member constituency

tabling member printed

uin

answer

is ministerial correction

date of answer

exactly:

or between:
and

answer text

answering member constituency

answering member printed

question first answered

answering member


label

tabling member


label

1016320

registered interest

date

28/11/2018

answering body

Department of Health and Social Care

answering dept id

answering dept short name

Health and Social Care

answering dept sort name

Health and Social Care

hansard heading

Medicines and Healthcare products Regulatory Agency

house id

legislature

25259

	pref label	House of Commons

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.

tabling member constituency

Newcastle-under-Lyme

tabling member printed

Paul Farrelly

uin

196736

answer

is ministerial correction

date of answer

03/12/2018

answer text

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. The Medicines and Healthcare products Regulatory Agency (MHRA) will continue to be the UK competent authority during this period. 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.

answering member constituency

Thurrock

answering member printed

Jackie Doyle-Price

question first answered

03/12/2018 18:29:34

answering member

4065

	label	Biography information for Dame Jackie Doyle-Price

tabling member

1436

	label	Biography information for Paul Farrelly