Accept Refuse

EUR-Lex Access to European Union law

This document is an excerpt from the EUR-Lex website

Document 22018D1752

Decision of the EEA Joint Committee No 18/2017 of 3 February 2017 amending Annex I (Veterinary and phytosanitary matters) and Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement [2018/1752]

OJ L 297, 22.11.2018, p. 22–23 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

In force

ELI: http://data.europa.eu/eli/dec/2018/1752/oj

22.11.2018   

EN

Official Journal of the European Union

L 297/22


DECISION OF THE EEA JOINT COMMITTEE

No 18/2017

of 3 February 2017

amending Annex I (Veterinary and phytosanitary matters) and Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement [2018/1752]

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) 2016/1002 of 17 June 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 AMTT, diquat, dodine, glufosinate and tritosulfuron in or on certain products (1) is to be incorporated into the EEA Agreement.

(2)

Commission Regulation (EU) 2016/1003 of 17 June 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 abamectin, acequinocyl, acetamiprid, benzovindiflupyr, bromoxynil, fludioxonil, fluopicolide, fosetyl, mepiquat, proquinazid, propamocarb, prohexadione and tebuconazole in or on certain products (2) is to be incorporated into the EEA Agreement.

(3)

Commission Regulation (EU) 2016/1015 of 17 June 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 1-naphthylacetamide, 1-naphthylacetic acid, chloridazon, fluazifop-P, fuberidazole, mepiquat and tralkoxydim in or on certain products (3) is to be incorporated into the EEA Agreement.

(4)

Commission Regulation (EU) 2016/1016 of 17 June 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 ethofumesate, etoxazole, fenamidone, fluoxastrobin and flurtamone in or on certain products (4) is to be incorporated into the EEA Agreement.

(5)

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.

(6)

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 1002: Commission Regulation (EU) 2016/1002 of 17 June 2016 (OJ L 167, 24.6.2016, p. 1),

32016 R 1003: Commission Regulation (EU) 2016/1003 of 17 June 2016 (OJ L 167, 24.6.2016, p. 46),

32016 R 1015: Commission Regulation (EU) 2016/1015 of 17 June 2016 (OJ L 172, 29.6.2016, p. 1),

32016 R 1016: Commission Regulation (EU) 2016/1016 of 17 June 2016 (OJ L 172, 29.6.2016, p. 22).’

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 1002: Commission Regulation (EU) 2016/1002 of 17 June 2016 (OJ L 167, 24.6.2016, p. 1),

32016 R 1003: Commission Regulation (EU) 2016/1003 of 17 June 2016 (OJ L 167, 24.6.2016, p. 46),

32016 R 1015: Commission Regulation (EU) 2016/1015 of 17 June 2016 (OJ L 172, 29.6.2016, p. 1),

32016 R 1016: Commission Regulation (EU) 2016/1016 of 17 June 2016 (OJ L 172, 29.6.2016, p. 22).’

Article 3

The texts of Regulations (EU) 2016/1002, (EU) 2016/1003, (EU) 2016/1015 and (EU) 2016/1016 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 February 2017, 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 February 2017.

For the EEA Joint Committee

The President

Claude MAERTEN


(1)  OJ L 167, 24.6.2016, p. 1.

(2)  OJ L 167, 24.6.2016, p. 46.

(3)  OJ L 172, 29.6.2016, p. 1.

(4)  OJ L 172, 29.6.2016, p. 22.

(*1)  No constitutional requirements indicated.


Top