The Human Medicines (Amendment) (Supply to Northern Ireland) Regulations 2021
These Regulations amend the Human Medicines Regulations 2012 (“the 2012 Regulations”), which govern the arrangements, across the United Kingdom, for the licensing, manufacture, wholesale dealing and sale or supply of human medicines for human use.
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Lifecycle
Department
Made
15 Dec 2021
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In force
01 Jan 2022
Enabling power
The Secretary of State, in exercise of the powers conferred by section 8C of, and paragraph 21 of Schedule 7 to, the European Union (Withdrawal) Act 2018, makes the following Regulations:
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