欧洲经济区联合委员会决定No 159/2012，修订欧洲经济区协议的附件II (技术法规、标准、检测和认证)
技术法规类型：欧盟Eurlex法规 来源：tbtmap
EURLEX ID：22012D0159
OJ编号：OJ L 341, 13.12.2012, p. 9-10
中文标题：欧洲经济区联合委员会决定No 159/2012，修订欧洲经济区协议的附件II (技术法规、标准、检测和认证)
原文标题：Decision of the EEA Joint Committee No 159/2012 of 28 September 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：2012-11-01
废止日期：2058-12-31
法规全文：查看欧盟官方文件
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13.12.2012 Official
Journal
of
the
European
Union
L
341/9
DECISION OF THE EEA JOINT COMMITTEE
No 159/2012
of 28 September 2012
amending Annex II (Technical regulations, standards, testing and certification) to the EEA
Agreement
THE EEA JOINT COMMITTEE,
to Regulation (EU) No 37/2010 on pharmacologically
active substances and their classification regarding
maximum residue limits in foodstuffs of animal origin,
Having regard to the Agreement on the European Economic
as regards the substance methylprednisolone ( 6 ) is to be
Area, as amended by the Protocol adjusting the Agreement
incorporated into the Agreement.
on the European Economic Area, hereinafter referred to as
‘the Agreement’, and in particular Article 98 thereof,
(7) Commission Implementing Regulation (EU) No
Whereas:
123/2012 of 13 February 2012 amending the Annex
to Regulation (EU) No 37/2010 on pharmacologically
active substances and their classification regarding
(1) Annex
II
to
the
Agreement
was
amended
by
Decision
of
maximum residue limits in foodstuffs of animal origin,
the EEA Joint Committee No 146/2012 of 13 July
as regards the substance monepantel ( 7 ) is to be incor
2012 ( 1 ).
porated into the Agreement.
(2) Commission
Implementing
Regulation
(EU)
No
84/2012
of 1 February 2012 amending the Annex to Regulation
(8) Commission Implementing Regulation (EU) No
(EU) No 37/2010 on pharmacologically active substances
201/2012 of 8 March 2012 amending the Annex to
and their classification regarding maximum residue limits
Regulation (EU) No 37/2010 on pharmacologically
in foodstuffs of animal origin, as regards the substance
active substances and their classification regarding
phenoxymethylpenicillin ( 2 ) is to be incorporated into the
maximum residue limits in foodstuffs of animal origin,
Agreement.
as regards the substance nitroxinil ( 8 ) is to be incor
porated into the Agreement.
(3) Commission
Implementing
Regulation
(EU)
No
85/2012
of 1 February 2012 amending the Annex to Regulation
(EU) No 37/2010 on pharmacologically active substances
(9) Commission Implementing Regulation (EU) No
and their classification regarding maximum residue limits
202/2012 of 8 March 2012 amending the Annex to
in foodstuffs of animal origin, as regards the substance
Regulation (EU) No 37/2010 on pharmacologically
altrenogest ( 3 ) is to be incorporated into the Agreement.
active substances and their classification regarding
maximum residue limits in foodstuffs of animal origin,
as regards the substance pegylated bovine granulocyte
(4) Commission
Implementing
Regulation
(EU)
No
86/2012
colony stimulating factor ( 9 ) is to be incorporated into
of 1 February 2012 amending the Annex to Regulation
the Agreement,
(EU) No 37/2010 on pharmacologically active substances
and their classification regarding maximum residue limits
in foodstuffs of animal origin, as regards the substance
lasalocid ( 4 ) is to be incorporated into the Agreement.
HAS ADOPTED THIS DECISION:
(5) Commission Implementing Regulation (EU) No
107/2012 of 8 February 2012 amending the Annex to
Article 1
Regulation (EU) No 37/2010 on pharmacologically active
substances and their classification regarding maximum
The following indents shall be added in point 13 (Commission
residue limits in foodstuffs of animal origin, as regards
Regulation (EU) No 37/2010) of Chapter XIII of Annex II to the
the substance octenidine dihydrochloride ( 5 ) is to be
Agreement:
incorporated into the Agreement.
(6) Commission Implementing Regulation (EU) No
‘— 32012 R 0084: Commission Implementing Regulation
122/2012 of 13 February 2012 amending the Annex
(EU) No 84/2012 of 1 February 2012 (OJ L 30,
2.2.2012, p. 1),
( 1 ) OJ L 309, 8.11.2012, p. 31.
( 2 ) OJ L 30, 2.2.2012, p. 1.
( 6 ) OJ L 40, 14.2.2012, p. 2.
( 3 ) OJ L 30, 2.2.2012, p. 4.
( 7 ) OJ L 40, 14.2.2012, p. 4.
( 4 ) OJ L 30, 2.2.2012, p. 6.
( 8 ) OJ L 71, 9.3.2012, p. 37.
( 5 ) OJ L 36, 9.2.2012, p. 25.
( 9 ) OJ L 71, 9.3.2012, p. 40.
L 341/10
EN
Official Journal of the European Union
13.12.2012
— 32012 R 0085: Commission Implementing Regulation
Article 2
(EU) No 85/2012 of 1 February 2012 (OJ L 30,
2.2.2012, p. 4),
The texts of Implementing Regulations (EU) No 84/2012, (EU)
No 85/2012, (EU) No 86/2012, (EU) No 107/2012, (EU) No
122/2012, (EU) No 123/2012, (EU) No 201/2012 and (EU) No
— 32012 R 0086: Commission Implementing Regulation
202/2012 in the Icelandic and Norwegian languages, to be
(EU) No 86/2012 of 1 February 2012 (OJ L 30,
published in the EEA Supplement to the Official Journal of the
2.2.2012, p. 6),
European Union, shall be authentic.
— 32012 R 0107: Commission Implementing Regulation
(EU) No 107/2012 of 8 February 2012 (OJ L 36,
Article 3
9.2.2012, p. 25),
This Decision shall enter into force on 1 November 2012,
provided that all the notifications under Article 103(1) of the
Agreement have been made to the EEA Joint Committee (*).
— 32012 R 0122: Commission Implementing Regulation
(EU) No 122/2012 of 13 February 2012 (OJ L 40,
14.2.2012, p. 2),
Article 4
— 32012 R 0123: Commission Implementing Regulation
This Decision shall be published in the EEA Section of, and in
(EU) No 123/2012 of 13 February 2012 (OJ L 40,
the EEA Supplement to, the Official Journal of the European
14.2.2012, p. 4),
Union.
— 32012 R 0201: Commission Implementing Regulation
(EU) No 201/2012 of 8 March 2012 (OJ L 71, 9.3.2012,
Done at Brussels, 28 September 2012.
p. 37),
For the EEA Joint Committee
— 32012 R 0202: Commission Implementing Regulation
(EU) No 202/2012 of 8 March 2012 (OJ L 71, 9.3.2012,
The President
p. 40).’.
Atle LEIKVOLL
(*) No constitutional requirements indicated.
13.12.2012 Official
Journal
of
the
European
Union
L
341/9
DECISION OF THE EEA JOINT COMMITTEE
No 159/2012
of 28 September 2012
amending Annex II (Technical regulations, standards, testing and certification) to the EEA
Agreement
THE EEA JOINT COMMITTEE,
to Regulation (EU) No 37/2010 on pharmacologically
active substances and their classification regarding
maximum residue limits in foodstuffs of animal origin,
Having regard to the Agreement on the European Economic
as regards the substance methylprednisolone ( 6 ) is to be
Area, as amended by the Protocol adjusting the Agreement
incorporated into the Agreement.
on the European Economic Area, hereinafter referred to as
‘the Agreement’, and in particular Article 98 thereof,
(7) Commission Implementing Regulation (EU) No
Whereas:
123/2012 of 13 February 2012 amending the Annex
to Regulation (EU) No 37/2010 on pharmacologically
active substances and their classification regarding
(1) Annex
II
to
the
Agreement
was
amended
by
Decision
of
maximum residue limits in foodstuffs of animal origin,
the EEA Joint Committee No 146/2012 of 13 July
as regards the substance monepantel ( 7 ) is to be incor
2012 ( 1 ).
porated into the Agreement.
(2) Commission
Implementing
Regulation
(EU)
No
84/2012
of 1 February 2012 amending the Annex to Regulation
(8) Commission Implementing Regulation (EU) No
(EU) No 37/2010 on pharmacologically active substances
201/2012 of 8 March 2012 amending the Annex to
and their classification regarding maximum residue limits
Regulation (EU) No 37/2010 on pharmacologically
in foodstuffs of animal origin, as regards the substance
active substances and their classification regarding
phenoxymethylpenicillin ( 2 ) is to be incorporated into the
maximum residue limits in foodstuffs of animal origin,
Agreement.
as regards the substance nitroxinil ( 8 ) is to be incor
porated into the Agreement.
(3) Commission
Implementing
Regulation
(EU)
No
85/2012
of 1 February 2012 amending the Annex to Regulation
(EU) No 37/2010 on pharmacologically active substances
(9) Commission Implementing Regulation (EU) No
and their classification regarding maximum residue limits
202/2012 of 8 March 2012 amending the Annex to
in foodstuffs of animal origin, as regards the substance
Regulation (EU) No 37/2010 on pharmacologically
altrenogest ( 3 ) is to be incorporated into the Agreement.
active substances and their classification regarding
maximum residue limits in foodstuffs of animal origin,
as regards the substance pegylated bovine granulocyte
(4) Commission
Implementing
Regulation
(EU)
No
86/2012
colony stimulating factor ( 9 ) is to be incorporated into
of 1 February 2012 amending the Annex to Regulation
the Agreement,
(EU) No 37/2010 on pharmacologically active substances
and their classification regarding maximum residue limits
in foodstuffs of animal origin, as regards the substance
lasalocid ( 4 ) is to be incorporated into the Agreement.
HAS ADOPTED THIS DECISION:
(5) Commission Implementing Regulation (EU) No
107/2012 of 8 February 2012 amending the Annex to
Article 1
Regulation (EU) No 37/2010 on pharmacologically active
substances and their classification regarding maximum
The following indents shall be added in point 13 (Commission
residue limits in foodstuffs of animal origin, as regards
Regulation (EU) No 37/2010) of Chapter XIII of Annex II to the
the substance octenidine dihydrochloride ( 5 ) is to be
Agreement:
incorporated into the Agreement.
(6) Commission Implementing Regulation (EU) No
‘— 32012 R 0084: Commission Implementing Regulation
122/2012 of 13 February 2012 amending the Annex
(EU) No 84/2012 of 1 February 2012 (OJ L 30,
2.2.2012, p. 1),
( 1 ) OJ L 309, 8.11.2012, p. 31.
( 2 ) OJ L 30, 2.2.2012, p. 1.
( 6 ) OJ L 40, 14.2.2012, p. 2.
( 3 ) OJ L 30, 2.2.2012, p. 4.
( 7 ) OJ L 40, 14.2.2012, p. 4.
( 4 ) OJ L 30, 2.2.2012, p. 6.
( 8 ) OJ L 71, 9.3.2012, p. 37.
( 5 ) OJ L 36, 9.2.2012, p. 25.
( 9 ) OJ L 71, 9.3.2012, p. 40.
L 341/10
EN
Official Journal of the European Union
13.12.2012
— 32012 R 0085: Commission Implementing Regulation
Article 2
(EU) No 85/2012 of 1 February 2012 (OJ L 30,
2.2.2012, p. 4),
The texts of Implementing Regulations (EU) No 84/2012, (EU)
No 85/2012, (EU) No 86/2012, (EU) No 107/2012, (EU) No
122/2012, (EU) No 123/2012, (EU) No 201/2012 and (EU) No
— 32012 R 0086: Commission Implementing Regulation
202/2012 in the Icelandic and Norwegian languages, to be
(EU) No 86/2012 of 1 February 2012 (OJ L 30,
published in the EEA Supplement to the Official Journal of the
2.2.2012, p. 6),
European Union, shall be authentic.
— 32012 R 0107: Commission Implementing Regulation
(EU) No 107/2012 of 8 February 2012 (OJ L 36,
Article 3
9.2.2012, p. 25),
This Decision shall enter into force on 1 November 2012,
provided that all the notifications under Article 103(1) of the
Agreement have been made to the EEA Joint Committee (*).
— 32012 R 0122: Commission Implementing Regulation
(EU) No 122/2012 of 13 February 2012 (OJ L 40,
14.2.2012, p. 2),
Article 4
— 32012 R 0123: Commission Implementing Regulation
This Decision shall be published in the EEA Section of, and in
(EU) No 123/2012 of 13 February 2012 (OJ L 40,
the EEA Supplement to, the Official Journal of the European
14.2.2012, p. 4),
Union.
— 32012 R 0201: Commission Implementing Regulation
(EU) No 201/2012 of 8 March 2012 (OJ L 71, 9.3.2012,
Done at Brussels, 28 September 2012.
p. 37),
For the EEA Joint Committee
— 32012 R 0202: Commission Implementing Regulation
(EU) No 202/2012 of 8 March 2012 (OJ L 71, 9.3.2012,
The President
p. 40).’.
Atle LEIKVOLL
(*) No constitutional requirements indicated.
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