The Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
Information
Type
Regulation
Regulated products
Medical Devices
Published
April 1, 2019
Last updated
May 26, 2020
Description
These Regulations are made in exercise of the powers conferred by section 8(1) of , paragraph 7(2) of Schedule 4 and paragraph 21 of Schedule 7 to the European Union (Withdrawal) Act 2018 (c. 16) (“the Withdrawal Act”) in order to address failures of retained EU law to operate effectively and other deficiencies (in particular under section 8(2)(a) of the Withdrawal Act) arising from the withdrawal of the UK from the European Union
Tags
Organization
Country / Region
United Kingdom
License
Open Government Licence 3.0 (United Kingdom)