Dáil Éireann Debate, Tuesday - 11 October 2016
466. Deputy Billy Kelleher asked 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]
Amharc ar fhreagraThe 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. |
