Statutory Instruments

The European Communities (Amendment of the Irish Medicines Board Act 1995) Regulations 2007

The purpose of these Regulations is to enable the recommendations or requirements, in respect of the use of a medicinal product otherwise than for their authorised indications or in respect of the use of an unauthorised medicinal product, in response to the suspected or confirmed spread of pathogenic agents, toxins, chemical agents or nuclear reaction any of which could cause harm, to be laid down by the Minister for Health and Children, rather than by the Irish Medicines Board

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