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Document 22013D0189

    Decision of the EEA Joint Committee No 189/2013 of 8 November 2013 amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement

    OJ L 92, 27.3.2014, p. 15–15 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

    Legal status of the document In force

    ELI: http://data.europa.eu/eli/dec/2013/189(2)/oj

    Date of document:
    08/11/2013
    Date of effect:
    09/11/2013; Entry into force See Art 3
    Date of end of validity:
    No end date
    Author:
    EEA Joint Committee
    Form:
    Decision adopted by bodies created by international agreements
    Treaty:
    Agreement on the European Economic Area
    Legal basis:
    Link
    Link
    Link
    Select all documents mentioning this document
    Modifies:
    Relation Act Comment Subdivision concerned From To
    Modifies 21994A0103(52) Addition chapter XIII point 13 indent 09/11/2013
    Instruments cited:
    Link

    27.3.2014   

    EN

    Official Journal of the European Union

    L 92/15

    DECISION OF THE EEA JOINT COMMITTEE

    No 189/2013

    of 8 November 2013

    amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement

    THE EEA JOINT COMMITTEE,

    Having regard to the Agreement on the European Economic Area (‘the EEA Agreement’), and in particular Article 98 thereof,

    Whereas:

    (1)

    Commission Implementing Regulation (EU) No 59/2013 of 23 January 2013 amending the Annex to Regulation (EU) No 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance monensin (1) is to be incorporated into the EEA Agreement.

    (2)

    Commission Implementing Regulation (EU) No 115/2013 of 8 February 2013 amending the Annex to Regulation (EU) No 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance diclazuril (2) is to be incorporated into the EEA Agreement.

    (3)

    Commission Implementing Regulation (EU) No 116/2013 of 8 February 2013 amending the Annex to Regulation (EU) No 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance eprinomectin (3) is to be incorporated into the EEA Agreement.

    (4)

    Annex II to the EEA Agreement should therefore be amended accordingly,

    HAS ADOPTED THIS DECISION:

    Article 1

    The following indents are added in point 13 (Commission Regulation (EU) No 37/2010) of Chapter XIII of Annex II to the EEA Agreement:

    ‘—

    32013 R 0059: Commission Implementing Regulation (EU) No 59/2013 of 23 January 2013 (OJ L 21, 24.1.2013, p. 21),

    —

    32013 R 0115: Commission Implementing Regulation (EU) No 115/2013 of 8 February 2013 (OJ L 38, 9.2.2013, p. 11),

    —

    32013 R 0116: Commission Implementing Regulation (EU) No 116/2013 of 8 February 2013 (OJ L 38, 9.2.2013, p. 14).’

    Article 2

    The texts of Implementing Regulations (EU) No 59/2013, (EU) No 115/2013 and (EU) No 116/2013 in the Icelandic and Norwegian languages, to be published in the EEA Supplement to the Official Journal of the European Union, shall be authentic.

    Article 3

    This Decision shall enter into force on 9 November 2013, provided that all the notifications under Article 103(1) of the EEA Agreement have been made (*1).

    Article 4

    This Decision shall be published in the EEA Section of, and in the EEA Supplement to, the Official Journal of the European Union.

    Done at Brussels, 8 November 2013.

    For the EEA Joint Committee

    The President

    Thórir IBSEN

    (1)   OJ L 21, 24.1.2013, p. 21.

    (2)   OJ L 38, 9.2.2013, p. 11.

    (3)   OJ L 38, 9.2.2013, p. 14.

    (*1)  No constitutional requirements indicated.

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