This document is an excerpt from the EUR-Lex website
Document 22019D1055
Decision of the EEA Joint Committee No 167/2017 of 22 September 2017 amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement [2019/1055]
Decision of the EEA Joint Committee No 167/2017 of 22 September 2017 amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement [2019/1055]
Decision of the EEA Joint Committee No 167/2017 of 22 September 2017 amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement [2019/1055]
IO L 174, 27.6.2019, p. 28–28
(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
- Date of document:
- 22/09/2017; Dáta ar glacadh
- Date of effect:
- 23/09/2017; Teacht i bhfeidhm Féach Airt. 3
- Date of end of validity:
- No end date
- Author:
- Comhchoiste an LEE
- Form:
- Cinneadh arna ghlacadh ag comhlachtaí a cruthaíodh trí chomhaontuithe idirnáisiúnta
- Legal basis:
-
- 21994A0103(01) - A98
- Link
- Link
- Link
- Select all documents mentioning this document No data available in the table
- Modifies:
-
Relation Act Comment Subdivision concerned From To Modifies 21994A0103(52) Cur le caibidil XIII pointe 12a 23/09/2017 - Instruments cited:
- Link
- EUROVOC descriptor:
- Subject matter:
- Directory code:
|
27.6.2019 |
EN |
Official Journal of the European Union |
L 174/28 |
DECISION OF THE EEA JOINT COMMITTEE
No 167/2017
of 22 September 2017
amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement [2019/1055]
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) 2017/880 of 23 May 2017 laying down rules on the use of a maximum residue limit established for a pharmacologically active substance in a particular foodstuff for another foodstuff derived from the same species and a maximum residue limit established for a pharmacologically active substance in one or more species for other species, in accordance with Regulation (EC) No 470/2009 of the European Parliament and of the Council (1) is to be incorporated into the EEA Agreement. |
|
(2) |
Annex II to the EEA Agreement should therefore be amended accordingly, |
HAS ADOPTED THIS DECISION:
Article 1
The following point is inserted after point 12 (Regulation (EC) No 470/2009 of the European Parliament and of the Council) of Chapter XIII of Annex II to the EEA Agreement:
|
‘12a. |
32017 R 0880: Commission Regulation (EU) 2017/880 of 23 May 2017 laying down rules on the use of a maximum residue limit established for a pharmacologically active substance in a particular foodstuff for another foodstuff derived from the same species and a maximum residue limit established for a pharmacologically active substance in one or more species for other species, in accordance with Regulation (EC) No 470/2009 of the European Parliament and of the Council (OJ L 135, 24.5.2017, p. 1).’ |
Article 2
The text of Regulation (EU) 2017/880 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 23 September 2017, 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, 22 September 2017.
For the EEA Joint Committee
The President
Sabine MONAUNI
(1) OJ L 135, 24.5.2017, p. 1.
(*1) No constitutional requirements indicated.
