The Medical Devices (Northern Ireland Protocol) Regulations 2021

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• Liquidator of Irvine and Fullarton Property Investment and Building Society v Cuthbertson
• European Union (Withdrawal) Act 2018
• Care Act 2014
• Consumer Rights Act 2015
• The Economic Growth (Regulatory Functions) Order 2017



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• Medical Devices Regulations 2002
• The Medicines (Products for Human Use) (Fees) Regulations 2016
• The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019
• The Blood Safety and Quality Regulations 2005
• The Blood Safety and Quality (Amendment) (EU Exit) Regulations 2019
• The Human Tissue (Quality and Safety for Human Application) Regulations 2007
• The Human Medicines Regulations 2012
• The Enterprise Act 2002 (Part 9 Restrictions on Disclosure of Information) (Amendment and Specification) Order 2003
• European Union (Withdrawal Agreement) Act 2020
• Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use
• Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (Text with EEA relevance. )
• Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use
• Commission Regulation (EU) No 722/2012 of 8 August 2012 concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured utilising tissues of animal origin Text with EEA relevance
• The Product Safety and Metrology etc. (Amendment etc.) (UK(NI) Indication) (EU Exit) Regulations 2020
• Medicines and Medical Devices Act 2021
• The Market Surveillance (Northern Ireland) Regulations 2021
• The Legislative and Regulatory Reform (Regulatory Functions) Order 2007