The Medical Devices (Amendment etc.) (EU Exit) Regulations 2020
Tuesday, 8 December 2020 19:02
The Medical Devices (Amendment etc.) (EU Exit) Regulations 2020
These Regulations are made in exercise of the powers in sections
8(1) and 8C of the European Union (Withdrawal) Act 2018 (c. 16) in
order to address failures of retained EU law to operate effectively
and other deficiencies (in particular under section 8(2)(a))
arising from the withdrawal of the United Kingdom from the European
Union, and in order to give effect to the Protocol on
Ireland/Northern Ireland in the withdrawal...Request free trial
The Medical
Devices (Amendment etc.) (EU Exit) Regulations 2020
These Regulations are made in exercise of the powers in sections
8(1) and 8C of the European Union (Withdrawal) Act 2018 (c. 16) in
order to address failures of retained EU law to operate effectively
and other deficiencies (in particular under section 8(2)(a))
arising from the withdrawal of the United Kingdom from the European
Union, and in order to give effect to the Protocol on
Ireland/Northern Ireland in the withdrawal agreement,
respectively.
Schedule 1 to these Regulations amends the Medical Devices
Regulations 2002 (S.I. 2002/618) in relation to Northern
Ireland.
The provisions in that Schedule ensure that S.I. 2002/618 continues
to operate effectively in light of the Ireland/Northern Ireland
Protocol following IP completion day 64 Schedule 2 to these
Regulations amends the Medical Devices (Amendment etc.) (EU Exit)
Regulations 2019 (S.I. 2019/791) and makes provision in respect of
the regulatory regime applying to medical devices in Great Britain
following IP completion day
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