Medicinal Products (Control of Wholesale Distribution) Regulations, 2007

This document cites

• Pre-Hospital Emergency Care Council (Establishment) Order, 2000 (Amendment) Order, 2004
• European Communities (Clinical Trials on Medicinal Products For Human Use) Regulations, 2004
• European Communities (Amendment of the Irish Medicines Board Act 1995) Regulations, 2007
• Medicinal Products (Control of Placing on the Market) Regulations, 2007
• Medicinal Products (Control of Manufacture) Regulations, 2007



See all quotations

• 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
• Directive 2002/98/EC of the European Parliament and of the Council of 27 January 2003 setting standards of quality and safety for the collection, testing, processing, storage and distribution of human blood and blood components and amending Directive 2001/83/EC
• Council Regulation (EEC) No 2309/93 of 22 July 1993 laying down Community procedures for the authorization and supervision of medicinal products for human and veterinary use and establishing a European Agency for the Evaluation of Medicinal Products
• 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
• Directive 2004/27/EC of the European Parliament and of the Council of 31 March 2004 amending Directive 2001/83/EC on the Community code relating to medicinal products for human use (Text with EEA relevance)
• Health (Alteration of Name of Department and Title of Minister) Order, 1997
• Medical Practitioners Act, 1978
• Medical Preparations (Wholesale Licences) Regulations, 1993