The Human Medicines (Amendments Relating to Hub and Spoke Dispensing etc.) Regulations 2025
These Regulations amend the Human Medicines Regulations 2012 (“the 2012 Regulations”), which govern the arrangements throughout the United Kingdom for the licensing, manufacture, marketing, wholesale dealing and the sale and supply of medicines for human use. They also amend the Medicines Act 1968 (“the 1968 Act”).
Lifecycle
Department
Made
25 Jun 2025
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In force
01 Oct 2025
Enabling power
In accordance with section 47(3) and (6)(c) of that Act, a draft of this instrument was laid before Parliament and the Northern Ireland Assembly and approved by a resolution of each House of Parliament and the Northern Ireland Assembly.
DocumentsOpen on legislation.gov.uk →