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Medicines Act 1968, Part V is up to date with all changes known to be in force on or before 04 January 2025. There are changes that may be brought into force at a future date. Changes that have been made appear in the content and are referenced with annotations.
Revised legislation carried on this site may not be fully up to date. Changes and effects are recorded by our editorial team in lists which can be found in the ‘Changes to Legislation’ area. Where those effects have yet to be applied to the text of the legislation by the editorial team they are also listed alongside the legislation in the affected provisions. Use the ‘more’ link to open the changes and effects relevant to the provision you are viewing.
Whole provisions yet to be inserted into this Act (including any effects on those provisions):
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Textual Amendments
F1S. 86 repealed (14.8.2012) by The Human Medicines Regulations 2012 (S.I. 2012/1916), reg. 1(2), Sch. 35 (with Sch. 32)
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Textual Amendments
F1S. 86 repealed (14.8.2012) by The Human Medicines Regulations 2012 (S.I. 2012/1916), reg. 1(2), Sch. 35 (with Sch. 32)
(1)The F2... Ministers may make regulations prohibiting the sale or supply of medicinal products otherwise than in containers which comply with such requirements as [F3the Ministers] consider necessary or expedient for any of the purposes specified in [F4subsection (3)], or for the purpose of preserving the quality of the products, and in particular, may by the regulations require such containers to be of such strength, to be made of such materials, and to be of such shapes or patterns, as may be prescribed.
(2)No person shall, in the course of a business carried on by him, sell or supply, or have in his possession for the purpose of sale or supply, any medicinal product in such circumstances as to contravene any requirements imposed by regulations under this section which are applicable to that product.
[F5(3)The purposes mentioned in subsection (1) are—
(a)securing that medicinal products are correctly described and readily identifiable;
(b)securing that any appropriate warning or other appropriate instruction or information is given, and that false or misleading information is not given, with respect to medicinal products;
(c)promoting safety in relation to medicinal products.]
Textual Amendments
F2Word in s. 87(1) omitted (1.10.2006) by virtue of The Veterinary Medicines Regulations 2006 (S.I. 2006/2407), reg. 1, Sch. 8 para. 44(a) (with regs. 2(4), 3)
F3Words in s. 87(1) substituted (1.10.2006) by The Veterinary Medicines Regulations 2006 (S.I. 2006/2407), reg. 1, Sch. 8 para. 44(b) (with regs. 2(4), 3)
F4Words in s. 87(1) substituted (14.8.2012) by The Human Medicines Regulations 2012 (S.I. 2012/1916), reg. 1(2), Sch. 34 para. 12(a) (with Sch. 32)
F5S. 87(3) inserted (14.8.2012) by The Human Medicines Regulations 2012 (S.I. 2012/1916), reg. 1(2), Sch. 34 para. 12(b) (with Sch. 32)
Modifications etc. (not altering text)
C1Pt. V (ss. 85–91) extended with modifications by S.I. 1985/1403, art. 3(1)
C2Ss. 85–88, 91 extended by S.I. 1984/187, art. 2
(1)Regulations made by the F6... Ministers may impose such requirements as, for any of the purposes specified in [F7section 87(3)] of this Act, [F8the Ministers] consider necessary or expedient with respect to any one or more of the following matters, that is to say—
(a)the colour of the products;
(b)the shape of the products; and
(c)distinctive marks to be displayed on the products.
(2)Regulations made under this section may provide that medicinal products of any such description, or falling within any such class, as may be specified in the regulations shall not except in such circumstances (if any) as may be so specified, be of any such colour or shape, or display any such mark, as may be so specified.
(3)No person shall, in the course of a business carried on by him, sell or supply, or have in his possession for the purpose of sale or supply, any medicinal product which contravenes any requirements imposed by regulations under this section.
Textual Amendments
F6Word in s. 88(1) omitted (1.10.2006) by virtue of The Veterinary Medicines Regulations 2006 (S.I. 2006/2407), reg. 1, Sch. 8 para. 45(a) (with regs. 2(4), 3)
F7Words in s. 88(1) substituted (14.8.2012) by The Human Medicines Regulations 2012 (S.I. 2012/1916), reg. 1(2), Sch. 34 para. 13 (with Sch. 32)
F8Words in s. 88(1) substituted (1.10.2006) by The Veterinary Medicines Regulations 2006 (S.I. 2006/2407), reg. 1, Sch. 8 para. 45(b) (with regs. 2(4), 3)
Modifications etc. (not altering text)
C3Pt. V (ss. 85–91) extended with modifications by S.I. 1985/1403, art. 3(1)
C4Ss. 85–88, 91 extended by S.I. 1984/187, art. 2
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Textual Amendments
F9S. 89 repealed (14.8.2012) by The Human Medicines Regulations 2012 (S.I. 2012/1916), reg. 1(2), Sch. 35 (with Sch. 32)
Modifications etc. (not altering text)
C5Pt. V (ss. 85–91) extended with modifications by S.I. 1985/1403, art. 3(1)
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Textual Amendments
F10S. 90 omitted (1.10.2006) by virtue of The Veterinary Medicines Regulations 2006 (S.I. 2006/2407), reg. 1, Sch. 8 para. 47 (with regs. 2(4), 3)
Modifications etc. (not altering text)
C6Pt. V (ss. 85–91) extended with modifications by S.I. 1985/1403, art. 3(1)
F11(1). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(2)Any regulations made under this Part of this Act may provide that any person who contravenes the regulations, or who contravenes the provisions of F12... section 87(2) of this Act F13..., shall be guilty of an offence and—
(a)shall be liable on summary conviction to a fine not exceeding £400 or such lesser sum as may be specified in the regulations, and
(b)if the regulations so provide, shall be liable on conviction on indictment to a fine or to imprisonment for a term not exceeding two years or to both.
(3)Without prejudice to the application of section 129(5) of this Act, any power to make regulations conferred by [F14section] 87 of this Act may be exercised so as to impose requirements either in relation to medicinal products generally or in relation to medicinal products of a particular description, or falling within a particular class, specified in the regulationsF15....
(4)In this Part of this Act “requirements” includes restrictions.
Textual Amendments
F11S. 91(1) repealed (14.8.2012) by virtue of The Human Medicines Regulations 2012 (S.I. 2012/1916), reg. 1(2), Sch. 34 para. 14(a), Sch. 35 (with Sch. 32)
F12Words in s. 91(2) omitted (14.8.2012) by virtue of The Human Medicines Regulations 2012 (S.I. 2012/1916), reg. 1(2), Sch. 34 para. 14(b) (with Sch. 32)
F13Words in s. 91(2) omitted (1.10.2006) by virtue of The Veterinary Medicines Regulations 2006 (S.I. 2006/2407), reg. 1, Sch. 8 para. 48(b) (with regs. 2(4), 3)
F14Word in s. 91(3) substituted (14.8.2012) by The Human Medicines Regulations 2012 (S.I. 2012/1916), reg. 1(2), Sch. 34 para. 14(c) (with Sch. 32)
F15Words in s. 91(3) omitted (1.10.2006) by virtue of The Veterinary Medicines Regulations 2006 (S.I. 2006/2407), reg. 1, Sch. 8 para. 48(c) (with regs. 2(4), 3)
Modifications etc. (not altering text)
C7Pt. V (ss. 85–91) extended with modifications by S.I. 1985/1403, art. 3(1)
C8Ss. 85–88, 91 extended by S.I. 1984/187, art. 2
C9S. 91 applied (with modifications) (3.4.1992) by S.I. 1992/605, reg. 2(1)(2), Sch.
C10Criminal Justice Act 1982 (c. 48, SIF 39:1), ss. 38 (increase of fines) and 46 (substitution of references to levels on the standard scale) apply (E.W.) and Criminal Procedure (Scotland) Act 1975 (c. 21, SIF 39:1), ss. 289F, 289G (increase of fines and substitution of references to levels on the standard scale) apply (S.) and S.I. 1984/703 (N.I. 3), art. 5 (substitution of references to levels on the standard scale) and art. 6 (increase of fines) apply (N.I.)
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