Medicines and Medical Devices Act 2021
Write the words of this act the way you think they should read. Solon shows your change as a redline against the published text and pins it to that exact text, so it can never be applied to wording you did not see.
Change 1
2 Power to make regulations about human medicines
(1) The appropriate authority may by regulations make provision specified in sections 3 to 7 amending or supplementing the law relating to human medicines. (2) In making regulations under subsection (1), the appropriate authority's overarching objective must be safeguarding public health. (3) In considering whether regulations under subsection (1) would contribute to this objective, the appropriate authority must have regard to— (a) the safety of human medicines; (b) the availability of human medicines; (c) the likelihood of the relevant part of the United Kingdom being seen as a favourable place in which to— (i) carry out research relating to human medicines, (ii) conduct clinical trials, or (iii) manufacture or supply human medicines. (4) Where regulations under subsection (1) may have an impact on the safety of human medicines, the appropriate authority may make the regulations only if the authority considers that the benefits of doing so outweigh the risks. (5) In subsection (3)(c), “relevant part of the United Kingdom” means— (a) so far as the regulations relate to England and Wales and Scotland, those parts of the United Kingdom, and (b) so far as the regulations relate to Northern Ireland, that part of the United Kingdom. (6) In this Part, “appropriate authority” means— (a) in relation to England and Wales and Scotland, the Secretary of State, and (b) in relation to Northern Ireland— (i) the Department of Health in Northern Ireland, or (ii) the Department of Health in Northern Ireland and the Secretary of State acting jointly.
2 Power to make regulations about human medicines
(1) The appropriate authority may by regulations make provision specified in sections 3 to 7 amending or supplementing the law relating to human medicines. (2) In making regulations under subsection (1), the appropriate authority's overarching objective must be safeguarding public health. (3) In considering whether regulations under subsection (1) would contribute to this objective, the appropriate authority must have regard to— (a) the safety of human medicines; (b) the availability of human medicines; (c) the likelihood of the relevant part of the United Kingdom being seen as a favourable place in which to— (i) carry out research relating to human medicines, (ii) conduct clinical trials, or (iii) manufacture or supply human medicines. (4) Where regulations under subsection (1) may have an impact on the safety of human medicines, the appropriate authority may make the regulations only if the authority considers that the benefits of doing so outweigh the risks. (5) In subsection (3)(c), “relevant part of the United Kingdom” means— (a) so far as the regulations relate to England and Wales and Scotland, those parts of the United Kingdom, and (b) so far as the regulations relate to Northern Ireland, that part of the United Kingdom. (6) In this Part, “appropriate authority” means— (a) in relation to England and Wales and Scotland, the Secretary of State, and (b) in relation to Northern Ireland— (i) the Department of Health in Northern Ireland, or (ii) the Department of Health in Northern Ireland and the Secretary of State acting jointly.
One line that says what changes, such as "Halve the dog tax".
Who it helps, what it costs, what it fixes. It is what persuades people to support it.
A proposal here is not law. Support on Solon is evidence that people want the change; the official route says what it takes to make it law.
Sign in to file your proposal. What you have written stays on this page.
Sign in to file itThink it through
Ask what your change would do, who would gain and who would bear a cost, and where something like it is already law. The assistant reads your draft as it stands, cites the law and the studies it finds, and takes no side. What you file stays yours.