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Document 22005D0131

Decision of the EEA Joint Committee No 131/2005 of 21 October 2005 amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement

OJ L 14, 19.1.2006, p. 18–19 (ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, NL, PL, PT, SK, SL, FI, SV)

⏵This document has been published in a special edition(s) (BG, RO, HR)

Legal status of the document In force

ELI: http://data.europa.eu/eli/dec/2005/131(2)/oj

Date of document:
21/10/2005
Date of effect:
22/10/2005; Entry into force See Art 3
Date of signature:
21/10/2005; Brussels
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) Repeal chapter XIII point 15f Text 22/10/2005
Modifies 21994A0103(52) Addition chapter XIII point 15x 22/10/2005
Instruments cited:
Link

19.1.2006   

EN

Official Journal of the European Union

L 14/18

DECISION OF THE EEA JOINT COMMITTEE

No 131/2005

of 21 October 2005

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, as amended by the Protocol adjusting the Agreement on the European Economic Area, hereinafter referred to as ‘the Agreement’, and in particular Article 98 thereof,

Whereas:

(1)

Annex II to the Agreement was amended by Decision of the EEA Joint Committee No 116/2005 (1).

(2)

Regulation (EC) No 273/2004 of the European Parliament and of the Council of 11 February 2004 on drug precursors (2) is to be incorporated into the Agreement.

(3)

Regulation (EC) No 273/2004 repeals Council Directive 92/109/EEC (3), which is incorporated into the Agreement and which is consequently to be repealed under the Agreement,

HAS DECIDED AS FOLLOWS:

Article 1

Chapter XIII of Annex II to the Agreement shall be amended as follows:

1.

The following point shall be added after point 15w (Directive 2004/23/EC of the European Parliament and of the Council):

‘15x.

32004 R 0273: Regulation (EC) No 273/2004 of the European Parliament and of the Council of 11 February 2004 on drug precursors (OJ L 47, 18.2.2004, p. 1).

The provisions of the Regulation shall, for the purposes of this Agreement, be read with the following adaptations:

(a)

The text of Article 11(2) shall not apply.

(b)

In Article 15 a reference is made to the Committee set up by Article 10 of Regulation (EEC) No 3677/90. When that Committee deals with matters covered by this Regulation the EFTA States shall participate fully in the work of the Committee, but shall not have the right to vote.’

2.

The text of point 15f (Council Directive 92/109/EEC) shall be deleted.

Article 2

The text of Regulation (EC) No 273/2004 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 22 October 2005, provided that all the notifications under Article 103(1) of the Agreement have been made to the EEA Joint Committee (*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, 21 October 2005.

For the EEA Joint Committee

The President

HSH Prinz Nikolaus von LIECHTENSTEIN

(1)   OJ L 339, 22.12.2005, p. 18.

(2)   OJ L 47, 18.2.2004, p. 1.

(3)   OJ L 370, 10.12.1992, p. 76.

(*1)  No constitutional requirements indicated.

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