Written answers
Tuesday, 11 October 2016
Department of Health
EU Directives
Billy Kelleher (Cork North Central, Fianna Fail)
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466. To ask the Minister for Health the outstanding EU directives that his Department or agencies under its remit are responsible for implementing, in tabular form; if the implementation of any of them require specific legislative change; and, if so, the details of same. [29771/16]
Simon Harris (Wicklow, Fine Gael)
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The EU Directives which the Department of Health has lead responsibility for transposing are set out in tabular form:
| Commission Proposal | Irish Legislative Transposition Measure | Deadline Date for Transposition |
|---|---|---|
| Commission Directive (EU) 2015/565 of 8 April 2015 amending Directive 2006/86/EC as regards certain technical requirements for the coding of human tissues and cells. | Secondary Legislation is required. | 29 October 2016. |
| Commission Directive (EU) 2015/566 of 8 April 2015 implementing Directive 2004/23/EC as regards the procedures for verifying the equivalent standards of quality and safety of imported tissues and cells. | Secondary legislation is required. | 29 October 2016. |
| Council Decision - subjecting the new psychoactive substance methyl 2-[[1-(cyclohexylmethyl)-1H-indole-3-carbonyl]amino]-3,3-dimethylbutanoate (MDMB-CHMICA) to control measures. | Secondary legislation is required. | 31 August 2017. |
| Commission Directive (EU) 2016/1214 of 25 July 2016 amending Directive 2005/62/EC as regards quality system standards and specifications for blood establishments. | Secondary legislation is required. | 15 February 2018. |
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