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Document 52012PC0098
Proposal for a COUNCIL DECISION on the position to be taken by the European Union in the EEA Joint Committeeconcerning an amendment to Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement.
Proposal for a COUNCIL DECISION on the position to be taken by the European Union in the EEA Joint Committeeconcerning an amendment to Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement.
Proposal for a COUNCIL DECISION on the position to be taken by the European Union in the EEA Joint Committeeconcerning an amendment to Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement.
/* COM/2012/098 final - 2012/0044 (NLE) */
52012PC0098
Proposal for a COUNCIL DECISION on the position to be taken by the European Union in the EEA Joint Committeeconcerning an amendment to Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement. /* COM/2012/098 final - 2012/0044 (NLE) */
EXPLANATORY MEMORANDUM 1. CONTEXT OF THE PROPOSAL In order to ensure the requisite legal
security and homogeneity of the Internal Market, the EEA Joint Committee is to
integrate all the relevant Union legislation into the EEA Agreement as soon as
possible after its adoption. 2. RESULTS OF CONSULTATIONS
WITH THE INTERESTED PARTIES AND IMPACT ASSESSMENTS The draft Decision of the EEA Joint
Committee (annexed to the proposed Council Decision) aims to amend Annex II
(Technical regulations, standards, testing and certification) to the EEA
Agreement by adding new Union acquis in this field. This concerns Regulation
(EC) No 470/2009 of the European Parliament and of the Council of 6 May 2009
laying down Community procedures for the establishment of residue limits of
pharmacologically active substances in foodstuffs of animal origin, repealing
Council Regulation (EEC) No 2377/90 and amending Directive 2001/82/EC of the
European Parliament and of the Council and Regulation (EC) No 726/2004 of the
European Parliament and of the Council, which is to be incorporated into the
Agreement. Regulation 470/2009 provides the possibility for the Commission and
Member States to request opinions from European Medicines Agency. In the
present draft EEA Joint Committee Decisions it is proposed that the EEA EFTA
States may request such opinions, but that these requests shall first be
addressed to the Commission which shall, where it considers that the request is
of common interest, forward it to the Agency for further processing 3. LEGAL ELEMENTS OF THE
PROPOSAL Article 1(3) of Council Regulation (EC) No
2894/94 concerning arrangements for implementing the EEA Agreement provides
that the Council establishes the position to be adopted on the Union’s behalf
on such Decisions, on a proposal from the Commission. The Commission submits the Draft Decision
of the EEA Joint Committee for adoption by the Council as the Union’s position.
The Commission would hope to be able to present it in the EEA Joint Committee
at the earliest possible opportunity. 2012/0044 (NLE) Proposal for a COUNCIL DECISION on the position to be taken by the
European Union in the EEA Joint Committee
concerning an amendment to Annex II (Technical regulations, standards, testing
and certification) to the EEA Agreement. THE COUNCIL OF THE EUROPEAN UNION, Having regard to the Treaty on the Functioning
of the European Union, and in particular Articles 43, 168(4)(b) and 218 (9) thereof, Having regard to the proposal from the
European Commission, Whereas: (1)
Annex II to the Agreement on the European
Economic Area, ("the EEA Agreement") contains specific provisions and
arrangements concerning technical regulations, standards, testing and
certification. (2)
Regulation (EC) No 470/2009 of the European
Parliament and of the Council of 6 May 2009 laying down Community procedures
for the establishment of residue limits of pharmacologically active substances
in foodstuffs of animal origin,[1]
should be incorporated in the EEA Agreement. Regulation (EC) No 470/2009 repeals
Council Regulation (EEC) No 2377/90 and amends Directive 2001/82/EC of the
European Parliament and of the Council and Regulation (EC) No 726/2004 of the
European Parliament and of the Council. Commission Regulation (EU) No 37/2010
of 22 December 2009 on pharmacologically active substances and their
classification regarding maximum residue limits in foodstuffs of animal origin[2], as corrected by OJ L 293,
11.11.2010, p. 72, is to be incorporated into the Agreement, (3)
Annex II to the EEA Agreement should therefore
be amended accordingly. (4)
The position of the Union within the EEA Joint
Committee should be based on the attached draft Decision, HAS ADOPTED THIS DECISION: Article 1 The position to be taken by the Union within
the EEA Joint Committee on the proposed amendment to Annex II to the EEA
Agreement shall be based on the draft Decision of the EEA Joint Committee
attached to this Decision. Article 2 This Decision shall enter into force on the
day of its adoption. Done at Brussels, 9.3.2012 For
the Council The
President ANNEX Draft DECISION
OF THE EEA JOINT COMMITTEE
No of 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 ... of …[3]. (2)
Regulation (EC) No 470/2009 of the European
Parliament and of the Council of 6 May 2009 laying down Community procedures
for the establishment of residue limits of pharmacologically active substances
in foodstuffs of animal origin, repealing Council Regulation (EEC) No 2377/90
and amending Directive 2001/82/EC of the European Parliament and of the Council
and Regulation (EC) No 726/2004 of the European Parliament and of the Council[4] is to be incorporated into the Agreement. (3)
Commission Regulation (EU) No 37/2010 of 22 December
2009 on pharmacologically active substances and their classification regarding
maximum residue limits in foodstuffs of animal origin[5], as corrected by OJ L 293,
11.11.2010, p. 72, is to be incorporated into the Agreement, HAS ADOPTED THIS DECISION: Article 1 Chapter XIII of Annex II to the Agreement
shall be amended as follows: 1. The following text shall be
inserted in point 12 (deleted): ‘32009 R 0470: Regulation (EC) No
470/2009 of the European Parliament and of the Council of 6 May 2009 laying down
Community procedures for the establishment of residue limits of
pharmacologically active substances in foodstuffs of animal origin, repealing
Council Regulation (EEC) No 2377/90 and amending Directive 2001/82/EC of the
European Parliament and of the Council and Regulation (EC) No 726/2004 of the
European Parliament and of the Council (OJ L 152, 16.6.2009,
p. 11). The provisions of the Regulation shall, for the
purposes of this Agreement, be read with the following adaptation: (a) References to other acts in the
Regulation shall be considered relevant to the extent and in the form that
those acts are incorporated into the Agreement. (b) An EFTA State may request the Agency
to issue an opinion according to Article 9(1), first paragraph of Article 11,
Article 15(1) and Article 27(2). Such a request shall, in the first place, be
addressed to the Commission which shall, where it considers that the request is
of common interest, forward it to the Agency for further processing.’ 2. The following text shall be inserted
in point 13 (deleted): ‘32010 R 0037: Commission Regulation
(EU) No 37/2010 of 22 December 2009 on pharmacologically active substances and
their classification regarding maximum residue limits in foodstuffs of animal
origin (OJ L 15, 20.1.2010, p. 1), as corrected by OJ L 293, 11.11.2010, p. 72.’ 3. The following indent shall be
added in points 15p (Directive 2001/82/EC of the European Parliament and of the
Council) and 15zb (Regulation (EC) No 726/2004 of the European Parliament and
of the Council): ‘- 32009 R 0470: Regulation (EC)
No 470/2009 of the European Parliament and of the Council of 6 May 2009 (OJ L 152, 16.6.2009, p. 11).’ Article 2 The texts of Regulations (EC) No 470/2009
and 37/2010, as corrected by OJ L 293, 11.11.2010, p. 72, 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 ,
provided that all the notifications under Article 103(1) of the Agreement have
been made to the EEA Joint Committee*. 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, . For the EEA Joint Committee The
President
The Secretaries
to the EEA Joint Committee
[1] OJ L 152, 16.6.2009, p. 11 [2] OJ L 15, 20.1.2010, p. 1. [3] OJ L … [4] OJ L 152, 16.6.2009, p. 11. [5] OJ L 15, 20.1.2010,
p. 1. * [No constitutional requirements indicated.]
[Constitutional requirements indicated.]