The Human Medicines (Coronavirus) (Further Amendments) Regulations 2020
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 medicines for human use.
Lifecycle
Department
Made
17 Dec 2020
—
Comes into force
TBC
Enabling power
The Secretary of State and the Minister of Health in Northern Ireland make the following Regulations in exercise of the powers conferred by section 2(2) and (5) of the European Communities Act 1972. They have been designated for the purposes of section 2(2) of that Act in relation to medicinal products.
DocumentsOpen on legislation.gov.uk →