The Human Medicines (Amendment Relating to Original Pack Dispensing) (England and Wales and Scotland) Regulations 2023
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Change 1
Title and introductory text
2023 No. 1015 Medicines The Human Medicines (Amendment Relating to Original Pack Dispensing) (England and Wales and Scotland) Regulations 2023 Made 13th September 2023 Coming into force 11th October 2023 The Secretary of State makes the following Regulations in exercise of the powers conferred by sections 2(1), 3(1)(j), (m) and (n) and 43(2) of the Medicines and Medical Devices Act 2021. The Secretary of State has carried out a public consultation in accordance with section 45(1) of that Act. In accordance with section 2(2) to (4) of that Act, the Secretary of State’s overarching objective in making these Regulations is safeguarding public health, the Secretary of State has had regard to the matters specified in section 2(3) of that Act and considers that, where these Regulations may have an impact on the safety of human medicines, the benefits of making these Regulations outweigh the risks. In accordance with section 47(3) and (6)(a) of that Act, a draft of these Regulations was laid before Parliament and approved by a resolution of each House of Parliament.
Title and introductory text
2023 No. 1015 Medicines The Human Medicines (Amendment Relating to Original Pack Dispensing) (England and Wales and Scotland) Regulations 2023 Made 13th September 2023 Coming into force 11th October 2023 The Secretary of State makes the following Regulations in exercise of the powers conferred by sections 2(1), 3(1)(j), (m) and (n) and 43(2) of the Medicines and Medical Devices Act 2021. The Secretary of State has carried out a public consultation in accordance with section 45(1) of that Act. In accordance with section 2(2) to (4) of that Act, the Secretary of State’s overarching objective in making these Regulations is safeguarding public health, the Secretary of State has had regard to the matters specified in section 2(3) of that Act and considers that, where these Regulations may have an impact on the safety of human medicines, the benefits of making these Regulations outweigh the risks. In accordance with section 47(3) and (6)(a) of that Act, a draft of these Regulations was laid before Parliament and approved by a resolution of each House of Parliament.
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