{"change_dates":[],"dossier":{"amendments":[],"changes":{"2017-12-16T06:09:03":[{"data":[{"body":"EC","commission":[],"date":"2017-12-06T00:00:00","docs":[{"celexid":"CELEX:52017PC0742:EN","title":"COM(2017)0742","type":"Legislative proposal published","url":"http://www.europarl.europa.eu/RegData/docs_autres_institutions/commission_europeenne/com/2017/0742/COM_COM(2017)0742_EN.pdf"}],"type":"Legislative proposal published"},{"body":"EP","committees":[{"body":"EP","committee":"AGRI","committee_full":"Agriculture and Rural Development","responsible":false},{"body":"EP","committee":"ENVI","committee_full":"Environment, Public Health and Food Safety","responsible":true}],"date":"2017-12-14T00:00:00","type":"Committee referral announced in Parliament, 1st reading/single reading"}],"path":["activities"],"type":"added"},{"data":[],"path":["other"],"type":"added"},{"data":[{"body":"EP","committee":"AGRI","committee_full":"Agriculture and Rural Development","responsible":false},{"body":"EP","committee":"ENVI","committee_full":"Environment, Public Health and Food Safety","responsible":true}],"path":["committees"],"type":"added"},{"data":{},"path":["links"],"type":"added"},{"data":{"Mandatory consultation of other institutions":"European Economic and Social Committee","dossier_of_the_committee":"ENVI/8/11809","instrument":"Directive","legal_basis":["Treaty on the Functioning of the EU TFEU 043-p2"],"reference":"2017/0329(COD)","stage_reached":"Awaiting committee decision","subject":["3.10.08 Animal health requirements, veterinary legislation and pharmacy","3.10.08.05 Animal diseases","4.60.04.04 Food safety"],"subtype":"Legislation","summary":["Amending Directive 92/66/EEC"],"title":"Measures for the control of Newcastle disease","type":"COD - Ordinary legislative procedure (ex-codecision procedure)"},"path":["procedure"],"type":"added"}],"2017-12-22T05:01:54":[{"data":{"Commissioner":"ANDRIUKAITIS Vytenis Povilas","DG":{"title":"Health and Food Safety","url":"http://ec.europa.eu/info/departments/health-and-food-safety_en"}},"path":["activities",0,"commission",0],"type":"added"},{"data":{"body":"EC","commissioner":"ANDRIUKAITIS Vytenis Povilas","dg":{"title":"Health and Food Safety","url":"http://ec.europa.eu/info/departments/health-and-food-safety_en"}},"path":["other",0],"type":"added"}],"2018-09-12T15:08:34":[{"data":[{"group":"S&D","mepref":"4f1ac963b819f25efd000132","name":"KADENBACH Karin"},{"group":"ECR","mepref":"4f1ac846b819f25efd0000da","name":"GIRLING Julie"},{"group":"ALDE","mepref":"4f1ac83bb819f25efd0000d5","name":"GERBRANDY Gerben-Jan"}],"path":["activities",1,"committees",1,"shadows"],"type":"added"},{"data":"2018-01-25T00:00:00","path":["activities",1,"committees",1,"date"],"type":"added"},{"data":[{"group":"EPP","mepref":"4f1adc41b819f207b300010c","name":"V\u0102LEAN Adina-Ioana"}],"path":["activities",1,"committees",1,"rapporteur"],"type":"added"},{"data":["
PURPOSE: to amend Council Directive 92/66/EEC\nintroducing Community measures for the control of Newcastle\ndisease, in order to bring it into line with the Treaty on the\nFunctioning of the European Union (TFEU) and the new official\ncontrol provisions in force.
\nPROPOSED ACT: Directive of the European Parliament and\nof the Council.
\nROLE OF THE EUROPEAN PARLIAMENT: the European\nParliament decides in accordance with the ordinary legislative\nprocedure on an equal footing with the Council.
\nBACKGROUND: Council\nDirective 92/66/EEC lays down the measures to be applied in the\nevent of an outbreak of Newcastle disease in poultry and certain\nbirds. The Directive confers on the Council, acting by a qualified\nmajority on a proposal from the Commission, the power to amend the\nDirectives Annexes.
\nThus, the Council may amend Annexes V, VI and VII to\nDirective 92/66/EEC which set out respectively (i) the indication\nof the European Union reference laboratory for Newcastle disease as\nwell as its functions and duties, (ii) the model form to be used by\nMember States in order to report on the disease situation and the\ncontrol measures applied; and (iii) the criteria to be applied by\nMember States for drawing up contingency plans specifying the\nnational measures to be implemented in the event of an outbreak the\ndisease.
\nIt is necessary to simplify and streamline the\nprocedures regarding the control of Newcastle disease, in\nparticular taking into account the new rules in relation to the\ndesignation of European Union reference laboratories provided for\nby Article 93 of Regulation\n(EU) 2017/625 of the European Parliament and of the Council,\nand also the new system of implementing acts provided for in\nArticle 291 of the Treaty on the Functioning of the European Union\n(TFEU).
\nThe current European reference laboratory (EURL) for\nNewcastle disease is located in the United Kingdom. Hence, it needs\nto be replaced by an EURL located in one of the other 27 Member\nStates in view of the United Kingdom exiting the EU. The\ncurrent procedure for designating an EURL for Newcastle disease is\nvia a Council Directive. This technical revision of the Directive\n92/66/EEC will enable the use of the required implementing\nprocedure to designate a new EURL for Newcastle disease within\nthe tight deadlines related to BREXIT.
\nCONTENT: the aim of this proposal is to amend\nCouncil Directive 92/66/EEC in order to ensure consistency with the\nTFEU and the new provisions on official controls with a view to\nsimplifying procedures. It aims to delete Annexes V, VI and VII of\nthat Directive and to confer on the Commission implementing powers\nin the matters covered by those Annexes. These powers should be\nexercised in accordance with Regulation (EU) No 182/2011 of the\nEuropean Parliament and of the Council (comitology\nRegulation).
\nThe proposal provides that the Commission shall\ndesignate, by means of implementing acts, a European Union\nreference laboratory for Newcastle disease. For the sake of\nclarity, it sets out the function and duties of the European Union\nreference laboratory for Newcastle Disease as well as the criteria\napplicable to the contingency plans to be established by Member\nStates in the event of the onset of the disease.
\nThe Committee on the Environment, Public Health and\nFood Safety adopted the report by Adina-Ioana VĂLEAN (EPP, RO)\non the proposal for a directive of the European Parliament and of\nthe Council amending Council Directive 92/66/EEC introducing\nCommunity measures for the control of Newcastle disease.
\nThe committee recommended that the European\nParliaments position adopted at first reading under the\nordinary legislative procedure should amend the Commission proposal\nto make it clear that the Directive should enter into force on\nthe day following its publication in the Official Journal of\nthe European Union.
\nMembers considered that this amendment is necessary\nin order for the Commission to designate\na new European Union reference laboratory for Newcastle disease\nwithin the tight deadlines related to BREXIT.
\nThe European Parliament adopted by 651 votes to 4,\nwith 48 abstentions, a legislative resolution on the proposal for a\ndirective of the European Parliament and of the Council amending\nCouncil Directive 92/66/EEC introducing Community measures for the\ncontrol of Newcastle disease.
\nThe technical revision of Directive 92/66/EEC shall\nmake it possible to use implementing acts to designate a new\nreference laboratory for Newcastle disease. Those implementing\npowers would be exercised in accordance with Regulation (EU) No\n182/2011 of the European Parliament and of the Council on\ncomitology.
\nFor the sake of clarity, the proposed amending\nDirective sets out the competences and tasks of the European\nUnion Reference Laboratory for Newcastle Disease and the criteria\nfor contingency plans. These plans shall allow access to\nfacilities, equipment, personnel and all other appropriate\nmaterials necessary for the rapid and efficient eradication of the\noutbreak of Newcastle disease. They shall give a precise indication\nof the vaccine requirements which each Member State deems necessary\nfor emergency vaccination.
\nThe Commission shall approve the contingency plans and\nany updates thereto, if necessary amended, in accordance with the\nexamination procedure.
\nThe European Parliaments position adopted at\nfirst reading under the ordinary legislative procedure amends the\nCommission proposal to make it clear that the Directive should\nenter into force on the day following its publication in the\nOfficial Journal of the European Union.
\nPURPOSE: to streamline measures for the control of\nNewcastle disease.
\nLEGISLATIVE ACT: Directive (EU) 2018/597 of the\nEuropean Parliament and of the Council amending Council Directive\n92/66/EEC introducing Community measures for the control of\nNewcastle disease.
\nCONTENT: Directive 92/66/EEC lays down the Union\ncontrol measures to be taken in the event of an outbreak of\nNewcastle disease in poultry, racing pigeons and other birds kept\nin captivity.
\nThis Directive consists of a technical revision of Directive\n92/66/EEC allowing the use of the implementing procedure to\ndesignate a new reference laboratory for Newcastle disease.\nThese implementing powers shall be exercised in accordance with\nRegulation (EU) No 182/2011 of the European Parliament and of the\nCouncil on comitology.
\nThe functions and duties of the European Union\nreference laboratory for Newcastle disease shall be:
\nEach Member State shall draw up a contingency\nplan, specifying the national measures to be implemented in the\nevent of an outbreak of Newcastle disease. The contingency plan\nshall be updated, as appropriate, to take account of developments\nin the situation.
\nENTRY INTO FORCE: 24.4.2018.
\nTRANSPOSITION: no later than 30.6.2018.
\nAPPLICATION: from\n1.1.2019.
\nPURPOSE: to amend Council Directive 92/66/EEC\nintroducing Community measures for the control of Newcastle\ndisease, in order to bring it into line with the Treaty on the\nFunctioning of the European Union (TFEU) and the new official\ncontrol provisions in force.
\nPROPOSED ACT: Directive of the European Parliament and\nof the Council.
\nROLE OF THE EUROPEAN PARLIAMENT: the European\nParliament decides in accordance with the ordinary legislative\nprocedure on an equal footing with the Council.
\nBACKGROUND: Council\nDirective 92/66/EEC lays down the measures to be applied in the\nevent of an outbreak of Newcastle disease in poultry and certain\nbirds. The Directive confers on the Council, acting by a qualified\nmajority on a proposal from the Commission, the power to amend the\nDirectives Annexes.
\nThus, the Council may amend Annexes V, VI and VII to\nDirective 92/66/EEC which set out respectively (i) the indication\nof the European Union reference laboratory for Newcastle disease as\nwell as its functions and duties, (ii) the model form to be used by\nMember States in order to report on the disease situation and the\ncontrol measures applied; and (iii) the criteria to be applied by\nMember States for drawing up contingency plans specifying the\nnational measures to be implemented in the event of an outbreak the\ndisease.
\nIt is necessary to simplify and streamline the\nprocedures regarding the control of Newcastle disease, in\nparticular taking into account the new rules in relation to the\ndesignation of European Union reference laboratories provided for\nby Article 93 of Regulation\n(EU) 2017/625 of the European Parliament and of the Council,\nand also the new system of implementing acts provided for in\nArticle 291 of the Treaty on the Functioning of the European Union\n(TFEU).
\nThe current European reference laboratory (EURL) for\nNewcastle disease is located in the United Kingdom. Hence, it needs\nto be replaced by an EURL located in one of the other 27 Member\nStates in view of the United Kingdom exiting the EU. The\ncurrent procedure for designating an EURL for Newcastle disease is\nvia a Council Directive. This technical revision of the Directive\n92/66/EEC will enable the use of the required implementing\nprocedure to designate a new EURL for Newcastle disease within\nthe tight deadlines related to BREXIT.
\nCONTENT: the aim of this proposal is to amend\nCouncil Directive 92/66/EEC in order to ensure consistency with the\nTFEU and the new provisions on official controls with a view to\nsimplifying procedures. It aims to delete Annexes V, VI and VII of\nthat Directive and to confer on the Commission implementing powers\nin the matters covered by those Annexes. These powers should be\nexercised in accordance with Regulation (EU) No 182/2011 of the\nEuropean Parliament and of the Council (comitology\nRegulation).
\nThe proposal provides that the Commission shall\ndesignate, by means of implementing acts, a European Union\nreference laboratory for Newcastle disease. For the sake of\nclarity, it sets out the function and duties of the European Union\nreference laboratory for Newcastle Disease as well as the criteria\napplicable to the contingency plans to be established by Member\nStates in the event of the onset of the disease.
\nThe Committee on the Environment, Public Health and\nFood Safety adopted the report by Adina-Ioana VĂLEAN (EPP, RO)\non the proposal for a directive of the European Parliament and of\nthe Council amending Council Directive 92/66/EEC introducing\nCommunity measures for the control of Newcastle disease.
\nThe committee recommended that the European\nParliaments position adopted at first reading under the\nordinary legislative procedure should amend the Commission proposal\nto make it clear that the Directive should enter into force on\nthe day following its publication in the Official Journal of\nthe European Union.
\nMembers considered that this amendment is necessary\nin order for the Commission to designate\na new European Union reference laboratory for Newcastle disease\nwithin the tight deadlines related to BREXIT.
\nThe European Parliament adopted by 651 votes to 4,\nwith 48 abstentions, a legislative resolution on the proposal for a\ndirective of the European Parliament and of the Council amending\nCouncil Directive 92/66/EEC introducing Community measures for the\ncontrol of Newcastle disease.
\nThe technical revision of Directive 92/66/EEC shall\nmake it possible to use implementing acts to designate a new\nreference laboratory for Newcastle disease. Those implementing\npowers would be exercised in accordance with Regulation (EU) No\n182/2011 of the European Parliament and of the Council on\ncomitology.
\nFor the sake of clarity, the proposed amending\nDirective sets out the competences and tasks of the European\nUnion Reference Laboratory for Newcastle Disease and the criteria\nfor contingency plans. These plans shall allow access to\nfacilities, equipment, personnel and all other appropriate\nmaterials necessary for the rapid and efficient eradication of the\noutbreak of Newcastle disease. They shall give a precise indication\nof the vaccine requirements which each Member State deems necessary\nfor emergency vaccination.
\nThe Commission shall approve the contingency plans and\nany updates thereto, if necessary amended, in accordance with the\nexamination procedure.
\nThe European Parliaments position adopted at\nfirst reading under the ordinary legislative procedure amends the\nCommission proposal to make it clear that the Directive should\nenter into force on the day following its publication in the\nOfficial Journal of the European Union.
\nPURPOSE: to streamline measures for the control of\nNewcastle disease.
\nLEGISLATIVE ACT: Directive (EU) 2018/597 of the\nEuropean Parliament and of the Council amending Council Directive\n92/66/EEC introducing Community measures for the control of\nNewcastle disease.
\nCONTENT: Directive 92/66/EEC lays down the Union\ncontrol measures to be taken in the event of an outbreak of\nNewcastle disease in poultry, racing pigeons and other birds kept\nin captivity.
\nThis Directive consists of a technical revision of Directive\n92/66/EEC allowing the use of the implementing procedure to\ndesignate a new reference laboratory for Newcastle disease.\nThese implementing powers shall be exercised in accordance with\nRegulation (EU) No 182/2011 of the European Parliament and of the\nCouncil on comitology.
\nThe functions and duties of the European Union\nreference laboratory for Newcastle disease shall be:
\nEach Member State shall draw up a contingency\nplan, specifying the national measures to be implemented in the\nevent of an outbreak of Newcastle disease. The contingency plan\nshall be updated, as appropriate, to take account of developments\nin the situation.
\nENTRY INTO FORCE: 24.4.2018.
\nTRANSPOSITION: no later than 30.6.2018.
\nAPPLICATION: from\n1.1.2019.
\n