Irish Medicines Board (Miscellaneous Provisions) Act, 2006

This document cites

• Misuse of Drugs Act, 1977
• Petty Sessions (Ireland) Act 1851
• Misuse of Drugs Act, 1984
• European Communities (Clinical Trials on Medicinal Products For Human Use) Regulations, 2004
• Medicinal Products (Amendment) Regulations, 2004



See all quotations

• Medical Preparations (Labelling and Package Leaflets) (Amendment) Regulations, 1999
• Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use
• Council Directive of 27 July 1976 on the approximation of the laws of the Member States relating to cosmetic products (76/768/EEC)
• Directive 2004/23/EC of the European Parliament and of the Council of 31 March 2004 on setting standards of quality and safety for the donation, procurement, testing, processing, preservation, storage and distribution of human tissues and cells
• Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use
• Commission Directive 95/17/EC of 19 June 1995 laying down detailed rules for the application of Council Directive 76/768/EEC as regards the non-inclusion of one or more ingredients on the list used for the labelling of cosmetic products (Text with EEA relevance)
• Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Union procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency (Text with EEA relevance)Text with EEA relevance
• Council Regulation (EC) No 111/2005 of 22 December 2004 laying down rules for the monitoring of trade between the Union and third countries in drug precursors
• Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
• Regulation (EC) No 178/2002 of the European Parliament and of the Council of 28 January 2002 laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety
• Council Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices
• Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products
• Trade Marks Act, 1996
• Medical Preparations (Licensing of Manufacture) Regulations, 1993
• Companies Act, 1963
• Medical Preparations (Licensing of Manufacture) (Amendment) Regulations, 1996
• Medicinal Products (Licensing and Sale) Regulations, 1998
• The Medical Preparations (Advertising) Regulations, 1993
• The Medical Preparations (Labelling & Package Leaflets) Regulations, 1993
• Medical Preparations (Wholesale Licences) (Amendment) Regulations, 1996
• Health Act, 1947
• Nurses Act, 1985
• Health Act, 1970
• Medical Practitioners Act, 1978
• Medical Preparations (Wholesale Licences) Regulations, 1993
• Dentists Act, 1985
• Medicinal Products (Prescription and Control of Supply) Regulations 2003
• European Communities (Health Act, 1947, Amendment of Sections 54 and 61) Regulations, 1991.
• European Communities (Cosmetic Products) Regulations, 2004