http://www.legislation.gov.uk/uksi/1994/276/contents/madeManufacturing licencesThe Medicines Act 1968 (Amendment) (No. 2) Regulations 1994Queen's Printer of Acts of Parliament2011-07-04MEDICINES These Regulations further amend the Medicines Act 1968 (“the Act”) to implement in part Council Directive 92/73/EEC (“the Homoeopathic Directive”) (OJ L 297, 13.10.92, p. 8) which widens the scope of Directives 65/65/EEC (OJ No. 22, 9.2.1965, p. 369/65) and 75/319/EEC (OJ No. L 147, 9.6.1975, p. 13) on the approximation of provisions laid down by law, regulation or administrative action relating to medicinal products and laying down additional provisions on homoeopathic medicinal products and Council Directive 92/27/EEC (OJ No. L113, 30.4.92, p. 8) (“the Labelling Directive”) which concerns the labelling of, and leaflets to be provided with, medicinal products. The Medicines Act 1968 (Amendment) (No. 2) Regulations 1994 1Citation, commencement and interpretation 2Revocation 3Section 7 of the Act — dealings with medicinal products 4Section 8 of the Act — manufacture and wholesale dealing 5Section 24 of the Act — duration and renewal of licence 6Section 28 of the Act — suspension etc. of the licence 7Section 86 of the Act—leaflets 8Section 91 of the Act — penalties 9Section 132 of the Act — interpretation This Statutory Instrument has been made in consequence of a defect in S.I. 1994/101 and is being issued free of charge to all known recipients of that Statutory Instrument. 1994 No. 276 Made 9th February 1994 Laid before Parliament 10th February 1994 Coming into force 13th February 1994 The Secretary of State for Health and the Minister for Agriculture, Fisheries and Food, acting jointly in exercise of the powers conferred on them by section 2(2) of the European Communities Act 1972, being designated for the purposes of that section in relation to medicinal products, hereby make the following Regulations: 1972 c. 68. S.I. 1972/1811.