S.I. No. 542/2007 - European Communities (Amendment of the Irish Medicines Board Act 1995) Regulations 2007 Skip to content Disclaimer Feedback Helpdesk Gaeilge Léim go dtí an t-ábhar Séanadh Aiseolas Deasc chabhrach English Gaeilge English Produced by the Office of the Attorney General Táirgthe ag Oifig an Ard-Aighne Home Legislation Acts of the Oireachtas Statutory Instruments Pre-1922 Legislation Constitution External Resources Bills (Houses of the Oireachtas) Iris Oifigiúil / Official Gazette Revised Acts (LRC) Classified List of Legislation (LRC) Translations (acts.
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- s)or rangeBliain nó blianta nó raon TypeCineál All Legislation Acts Statutory Instruments Advanced SearchCuardach Casta HomeBaile Statutory InstrumentsIonstraimí Reachtúla 2007 S.I. No. 542/2007 - European Communities (Amendment of the Irish Medicines Board Act 1995) Regulations 2007 S.I. No. 542/2007 - European Communities (Amendment of the Irish Medicines Board Act 1995) Regulations 2007 AmendmentsLeasuithe Download PDF Íoslódáil PDF S.I. No. 542 of 2007 EUROPEAN COMMUNITIES (AMENDMENT OF THE IRISH MEDICINES BOARD ACT 1995) REGULATIONS 2007 Notice of the making of this Statutory Instrument was published in “Iris Oifigiúil” of 31st July, 2007. I, MARY HARNEY, Minister for Health and Children, in exercise of the powers conferred on me by section 3 of the European Communities Act 1972 (No. 27 of 1972) and for the purpose of giving effect to Directive 2001/83/EC 1 , hereby make the following Regulations: 1. These Regulations may be cited as the European Communities (Amendment of the Irish Medicines Board Act 1995 ) Regulations 2007. 2. These Regulations shall come into operation on the 23rd July 2007. 3. Section 4
(1)(
- b)of the Irish Medicines Board Act 1995 (as substituted by section 11(a)(
- ii)of the Irish Medicines Board (Miscellaneous Provisions) Act 2006 (No. 3 of 2006)) is hereby amended by inserting “other than those powers conferred by Article 5.3 of the said Directive,” after “6 November 2001,”. 4. For the purposes of Article 5.3 of Directive 2001/83/EC, as amended by Directive 2004/27/EC 2 , the competent authority shall be the Minister for Health and Children. GIVEN under my Official Seal, 20 July 2007 MARY HARNEY Minister for Health and Children EXPLANATORY NOTE (This note is not part of the Instrument and does not purport to be a legal interpretation) 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. 1 OJ No. L.311, 28.11.2001, p.67 - 128. 2 OJ No. L.136, 30.04.2004, p. 34 - 57. Privacy Statement Accessibility European Legislation Identifier (PDF) Open Data License Ráiteas Príobháideachais Inrochtaineacht Aitheantóir Eorpach Reachtaíochta (ELI) Ceadúnas Sonraí Oscailte Liosta Fianán © Government of Ireland. Oireachtas Copyright Material is reproduced with the permission of the Houses of the Oireachtas © Rialtas na hÉireann. Atáirgtear ábhar faoi Chóipcheart le cead ó Thithe an Oireachtais