欧洲经济区联合委员会决定 No 84/2012,修订欧洲经济区协议附件II (技术法规, 标准, 检测与认证)
技术法规类型:欧盟Eurlex法规 来源:tbtmap
EURLEX ID:22012D0084
OJ编号:OJ L 248, 13.9.2012, p. 21-21
中文标题:欧洲经济区联合委员会决定 No 84/2012,修订欧洲经济区协议附件II (技术法规, 标准, 检测与认证)
原文标题:Decision of the EEA Joint Committee No 84/2012 of 30 April 2012 amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement
分类:11.40.10.10_欧洲自由贸易区(EFTA)国家
文件类型:外部关系 Decision|决定
生效日期:2012-05-01
废止日期:2058-12-31
法规全文:查看欧盟官方文件
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13.9.2012 Official
Journal
of
the
European
Union L
248/21
DECISION OF THE EEA JOINT COMMITTEE
No 84/2012
of 30 April 2012
amending Annex II (Technical regulations, standards, testing and certification) to the EEA
Agreement
THE EEA JOINT COMMITTEE,
‘, as amended by:
Having regard to the Agreement on the European Economic
— 32010 R 0890: Commission Regulation (EU)
Area, as amended by the Protocol adjusting the Agreement
No 890/2010 of 8 October 2010 (OJ L 266, 9.10.2010,
on the European Economic Area, hereinafter referred to as
p. 1),
‘the Agreement’, and in particular Article 98 thereof,
Whereas:
— 32010 R 0914: Commission Regulation (EU)
No 914/2010 of 12 October 2010 (OJ L 269,
13.10.2010, p. 5).’
(1) Annex
II
to
the
Agreement
was
amended
by
Decision
of
the EEA Joint Committee No 47/2012 of 30 March
2012 ( 1 ).
Article 2
The texts of Regulations (EU) No
890/2010 and (EU)
(2) Commission
Regulation
(EU)
No
890/2010
of
8
October No 914/2010 in the Icelandic and Norwegian languages, to
2010 amending the Annex to Regulation (EU)
be published in the EEA Supplement to the Official Journal of
No 37/2010 on pharmacologically active substances
the European Union, shall be authentic.
and their classification regarding maximum residue
limits in foodstuffs of animal origin, as regards the
substance derquantel ( 2 ) is to be incorporated into the
Article 3
Agreement.
This Decision shall enter into force on 1 May 2012, provided
that all the notifications under Article 103(1) of the Agreement
(3) Commission Regulation (EU) No
914/2010 of have been made to the EEA Joint Committee (*).
12 October 2010 amending the Annex to Regulation
(EU) No 37/2010 on pharmacologically active substances
and their classification regarding maximum residue limits
Article 4
in foodstuffs of animal origin, as regards the substance
This Decision shall be published in the EEA Section of, and in
sodium salicylate ( 3 ) is to be incorporated into the
the EEA Supplement to, the Official Journal of the European
Agreement,
Union.
HAS ADOPTED THIS DECISION:
Done at Brussels, 30 April 2012.
Article 1
For the EEA Joint Committee
The following shall be added in point 13 (Commission Regu
lation (EU) No 37/2010) of Chapter XIII of Annex II to the
The Acting President
Agreement:
Gianluca GRIPPA
( 1 ) OJ L 207, 2.8.2012, p. 27.
( 2 ) OJ L 266, 9.10.2010, p. 1.
( 3 ) OJ L 269, 13.10.2010, p. 5. (*)
No
constitutional
requirements
indicated.
13.9.2012 Official
Journal
of
the
European
Union L
248/21
DECISION OF THE EEA JOINT COMMITTEE
No 84/2012
of 30 April 2012
amending Annex II (Technical regulations, standards, testing and certification) to the EEA
Agreement
THE EEA JOINT COMMITTEE,
‘, as amended by:
Having regard to the Agreement on the European Economic
— 32010 R 0890: Commission Regulation (EU)
Area, as amended by the Protocol adjusting the Agreement
No 890/2010 of 8 October 2010 (OJ L 266, 9.10.2010,
on the European Economic Area, hereinafter referred to as
p. 1),
‘the Agreement’, and in particular Article 98 thereof,
Whereas:
— 32010 R 0914: Commission Regulation (EU)
No 914/2010 of 12 October 2010 (OJ L 269,
13.10.2010, p. 5).’
(1) Annex
II
to
the
Agreement
was
amended
by
Decision
of
the EEA Joint Committee No 47/2012 of 30 March
2012 ( 1 ).
Article 2
The texts of Regulations (EU) No
890/2010 and (EU)
(2) Commission
Regulation
(EU)
No
890/2010
of
8
October No 914/2010 in the Icelandic and Norwegian languages, to
2010 amending the Annex to Regulation (EU)
be published in the EEA Supplement to the Official Journal of
No 37/2010 on pharmacologically active substances
the European Union, shall be authentic.
and their classification regarding maximum residue
limits in foodstuffs of animal origin, as regards the
substance derquantel ( 2 ) is to be incorporated into the
Article 3
Agreement.
This Decision shall enter into force on 1 May 2012, provided
that all the notifications under Article 103(1) of the Agreement
(3) Commission Regulation (EU) No
914/2010 of have been made to the EEA Joint Committee (*).
12 October 2010 amending the Annex to Regulation
(EU) No 37/2010 on pharmacologically active substances
and their classification regarding maximum residue limits
Article 4
in foodstuffs of animal origin, as regards the substance
This Decision shall be published in the EEA Section of, and in
sodium salicylate ( 3 ) is to be incorporated into the
the EEA Supplement to, the Official Journal of the European
Agreement,
Union.
HAS ADOPTED THIS DECISION:
Done at Brussels, 30 April 2012.
Article 1
For the EEA Joint Committee
The following shall be added in point 13 (Commission Regu
lation (EU) No 37/2010) of Chapter XIII of Annex II to the
The Acting President
Agreement:
Gianluca GRIPPA
( 1 ) OJ L 207, 2.8.2012, p. 27.
( 2 ) OJ L 266, 9.10.2010, p. 1.
( 3 ) OJ L 269, 13.10.2010, p. 5. (*)
No
constitutional
requirements
indicated.
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