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Document 22017D2126

    Decision of the EEA Joint Committee No 108/2016 of 3 June 2016 amending Annex I (Veterinary and phytosanitary matters) and Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement [2017/2126]

    OJ L 308, 23.11.2017, p. 6–7 (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/2017/2126/oj

    23.11.2017   

    EN

    Official Journal of the European Union

    L 308/6


    DECISION OF THE EEA JOINT COMMITTEE

    No 108/2016

    of 3 June 2016

    amending Annex I (Veterinary and phytosanitary matters) and Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement [2017/2126]

    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 Regulation (EU) 2016/46 of 18 January 2016 amending Annex III to Regulation (EC) No 396/2005 of the European Parliament and of the Council as regards maximum residue levels for oxadixyl and spinetoram in or on certain products (1) is to be incorporated into the EEA Agreement.

    (2)

    Commission Regulation (EU) 2016/53 of 19 January 2016 amending Annexes II and III to Regulation (EC) No 396/2005 of the European Parliament and of the Council as regards maximum residue levels for diethofencarb, mesotrione, metosulam and pirimiphos-methyl in or on certain products (2) is to be incorporated into the EEA Agreement.

    (3)

    Commission Regulation (EU) 2016/60 of 19 January 2016 amending Annexes II and III to Regulation (EC) No 396/2005 of the European Parliament and of the Council as regards maximum residue levels for chlorpyrifos in or on certain products (3) is to be incorporated into the EEA Agreement.

    (4)

    Commission Regulation (EU) 2016/67 of 19 January 2016 amending Annexes II, III and V to Regulation (EC) No 396/2005 of the European Parliament and of the Council as regards maximum residue levels for ametoctradin, chlorothalonil, diphenylamine, flonicamid, fluazinam, fluoxastrobin, halauxifen-methyl, propamocarb, prothioconazole, thiacloprid and trifloxystrobin in or on certain products (4) is to be incorporated into the EEA Agreement.

    (5)

    Commission Regulation (EU) 2016/75 of 21 January 2016 amending Annex III to Regulation (EC) No 396/2005 of the European Parliament and of the Council as regards maximum residue levels for fosetyl in or on certain products (5) is to be incorporated into the EEA Agreement.

    (6)

    This Decision concerns legislation regarding feedingstuffs and foodstuffs. Legislation regarding feedingstuffs and foodstuffs shall not apply to Liechtenstein as long as the application of the Agreement between the European Community and the Swiss Confederation on trade in agricultural products is extended to Liechtenstein, as specified in the sectoral adaptations to Annex I and the introduction to Chapter XII of Annex II to the EEA Agreement. This Decision is therefore not to apply to Liechtenstein.

    (7)

    Annexes I and II to the EEA Agreement should therefore be amended accordingly,

    HAS ADOPTED THIS DECISION:

    Article 1

    The following indents are added in point 40 (Regulation (EC) No 396/2005 of the European Parliament and of the Council) of Chapter II of Annex I to the EEA Agreement:

    ‘—

    32016 R 0046: Commission Regulation (EU) 2016/46 of 18 January 2016 (OJ L 12, 19.1.2016, p. 28),

    32016 R 0053: Commission Regulation (EU) 2016/53 of 19 January 2016 (OJ L 13, 20.1.2016, p. 12),

    32016 R 0060: Commission Regulation (EU) 2016/60 of 19 January 2016 (OJ L 14, 21.1.2016, p. 1),

    32016 R 0067: Commission Regulation (EU) 2016/67 of 19 January 2016 (OJ L 15, 22.1.2016, p. 2),

    32016 R 0075: Commission Regulation (EU) 2016/75 of 21 January 2016 (OJ L 16, 23.1.2016, p. 8).’

    Article 2

    The following indents are added in point 54zzy (Regulation (EC) No 396/2005 of the European Parliament and of the Council) of Chapter XII of Annex II to the EEA Agreement:

    ‘—

    32016 R 0046: Commission Regulation (EU) 2016/46 of 18 January 2016 (OJ L 12, 19.1.2016, p. 28),

    32016 R 0053: Commission Regulation (EU) 2016/53 of 19 January 2016 (OJ L 13, 20.1.2016, p. 12),

    32016 R 0060: Commission Regulation (EU) 2016/60 of 19 January 2016 (OJ L 14, 21.1.2016, p. 1),

    32016 R 0067: Commission Regulation (EU) 2016/67 of 19 January 2016 (OJ L 15, 22.1.2016, p. 2),

    32016 R 0075: Commission Regulation (EU) 2016/75 of 21 January 2016 (OJ L 16, 23.1.2016, p. 8).’

    Article 3

    The texts of Regulations (EU) 2016/46, (EU) 2016/53, (EU) 2016/60, (EU) 2016/67 and (EU) 2016/75 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 4

    This Decision shall enter into force on 4 June 2016, provided that all the notifications under Article 103(1) of the EEA Agreement have been made (*1).

    Article 5

    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, 3 June 2016.

    For the EEA Joint Committee

    The President

    Claude MAERTEN


    (1)   OJ L 12, 19.1.2016, p. 28.

    (2)   OJ L 13, 20.1.2016, p. 12.

    (3)   OJ L 14, 21.1.2016, p. 1.

    (4)   OJ L 15, 22.1.2016, p. 2.

    (5)   OJ L 16, 23.1.2016, p. 8.

    (*1)  No constitutional requirements indicated.


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