The Human Medicines (Amendments relating to Registered Dental Hygienists, Registered Dental Therapists and Registered Pharmacy Technicians) Regulations 2024
These Regulations amend the Human Medicines Regulations 2012 (S.I. 2012/1916) (“HMRs”) which govern the arrangements across the United Kingdom for the licensing, manufacture, wholesale dealing and sale or supply of medicines for human use. The amendments extend to the whole of the United Kingdom.
Lifecycle
Department
Made
29 May 2024
—
Comes into force
TBC
Enabling power
the Act The Secretary of State in relation to England and Wales and Scotland and the Department of Health in Northern Ireland and the Secretary of State acting jointly in relation to Northern Ireland make these Regulations in exercise of the powers conferred by sections 2(1), 3(1)(n), 3(2)(a), (c) and (d) and 43(2) of the Medicines and Medical Devices Act 2021(“”). The Secretary of State and the Department of Health in Northern Ireland have carried out a public consultation in accordance with section 45(1) of the Act. In accordance with section 2(2) to (4) of the Act, the Secretary of State’s and the Department of Health in Northern Ireland’s overarching objective in making these Regulations is safeguarding public health. The Secretary of State and the Department of Health in Northern Ireland have had regard to the matters specified in section 2(3) of the Act and consider that, where these Regulations may have an impact on the safety of human medicines, the benefit of making these Regulations outweigh the risks. In accordance with section 47(3) and (6)(c) of the 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 →