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Document 22018D1172

Decision of the EEA Joint Committee No 234/2016 of 2 December 2016 amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement [2018/1172]

OJ L 215, 23.8.2018, p. 30–31 (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/2018/1172/oj

23.8.2018   

EN

Official Journal of the European Union

L 215/30


DECISION OF THE EEA JOINT COMMITTEE

No 234/2016

of 2 December 2016

amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement [2018/1172]

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 Decision (EU) 2016/1174 of 15 July 2016 on the terms and conditions of the authorisation of a biocidal product containing difenacoum referred by Spain in accordance with Article 36 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (1) is to be incorporated into the EEA Agreement.

(2)

Commission Implementing Decision (EU) 2016/1175 of 15 July 2016 on the terms and conditions of the authorisation of a biocidal product containing spinosad referred by the United Kingdom in accordance with Article 36 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (2) is to be incorporated into the EEA Agreement.

(3)

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

HAS ADOPTED THIS DECISION:

Article 1

The following points are inserted after point 12nnx (Commission Implementing Decision (EU) 2016/904) of Chapter XV of Annex II to the EEA Agreement:

‘12nny.

32016 D 1174: Commission Implementing Decision (EU) 2016/1174 of 15 July 2016 on the terms and conditions of the authorisation of a biocidal product containing difenacoum referred by Spain in accordance with Article 36 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (OJ L 193, 19.7.2016, p. 110).

12nnz.

32016 D 1175: Commission Implementing Decision (EU) 2016/1175 of 15 July 2016 on the terms and conditions of the authorisation of a biocidal product containing spinosad referred by the United Kingdom in accordance with Article 36 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (OJ L 193, 19.7.2016, p. 113).’

Article 2

The texts of Implementing Decision (EU) 2016/1174 and (EU) 2016/1175 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 3 December 2016, 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, 2 December 2016.

For the EEA Joint Committee

The President

Bergdís ELLERTSDÓTTIR


(1)  OJ L 193, 19.7.2016, p. 110.

(2)  OJ L 193, 19.7.2016, p. 113.

(*1)  No constitutional requirements indicated.


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