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
14 Interpretation of Part 3 and supplementary provision
(1) In this Part— “active substance” means any substance or mixture of substances intended to be used in the manufacture of a veterinary medicine that, when used in its production, becomes an active ingredient of that medicine; “appropriate authority” has the meaning given by section 10(6); “manufacture” includes assembly; “marketing authorisation” means an authorisation to market a veterinary medicine in the United Kingdom; “veterinary medicine” means a veterinary medicinal product within the meaning given by regulation 2 of the Veterinary Medicines Regulations 2013 (S.I. 2013/2033). (2) In the Animals (Scientific Procedures) Act 1986, in section 2 (regulated procedures), in subsection (8)(d), after “the Veterinary Medicines Regulations 2011” insert “ or the Veterinary Medicines Regulations 2013 ”.
14 Interpretation of Part 3 and supplementary provision
(1) In this Part— “active substance” means any substance or mixture of substances intended to be used in the manufacture of a veterinary medicine that, when used in its production, becomes an active ingredient of that medicine; “appropriate authority” has the meaning given by section 10(6); “manufacture” includes assembly; “marketing authorisation” means an authorisation to market a veterinary medicine in the United Kingdom; “veterinary medicine” means a veterinary medicinal product within the meaning given by regulation 2 of the Veterinary Medicines Regulations 2013 (S.I. 2013/2033). (2) In the Animals (Scientific Procedures) Act 1986, in section 2 (regulated procedures), in subsection (8)(d), after “the Veterinary Medicines Regulations 2011” insert “ or the Veterinary Medicines Regulations 2013 ”.
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