Statutory Instruments

The Medicinal Products (Control of Manufacture) (Amendment) Regulations 2012

These Regulations amend the Medicinal Products (Control of Manufacture) Regulations 2007 (S.I. No. 539 of 2007)

These Regulations give further effect to Directive 2008/29/EC of the European Parliament and of the Council of 11 March 2008, Directive 2009/53/EC of the European Parliament and of the Council of 18 June 2009 and Directive 2010/84/EU of the European Parliament and of the Council of 15 December 2010

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