Medicinal Products (Control of Advertising) Regulations, 2007
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Medicinal Products (Control of Advertising) Regulations, 2007
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- Misuse of Drugs Act, 1977
- Medicinal Products (Control of Placing on the Market) Regulations, 2007
- 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
