Commission Implementing Decision of 10 February 2012 as regards the renewal of the authorisation for continued marketing of products containing, consisting of, or produced from genetically modified soybean 40-3-2 (MON-Ø4Ø32-6) pursuant to Regulation (EC) No 1829/2003 of the European Parliament and of the Council (notified under document C(2012) 700) (Only the Dutch and the French texts are authentic) (Text with EEA relevance) (2012/82/EU) (revoked)
EU Decision 2012/82 · Adopted 10 February 2012 · Extends to United Kingdom
Commission Implementing Decision
of 10 February 2012
as regards the renewal of the authorisation for continued marketing of products containing, consisting of, or produced from genetically modified soybean 40-3-2 (MON-Ø4Ø32-6) pursuant to Regulation (EC) No 1829/2003 of the European Parliament and of the Council
(notified under document C(2012) 700)
(Only the Dutch and the French texts are authentic)
(Text with EEA relevance)
(2012/82/EU) (revoked)
F1. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Annotations to the whole text
Textual amendments
- F1
Decision revoked (1.4.2025) by The Food and Feed (Regulated Products) (Amendment, Revocation, Consequential and Transitional Provision) Regulations 2025 (S.I. 2025/361), reg. 1(2), Sch. 6 para. 12 (with reg. 23)
Contents
- 1Genetically modified organism and unique identifier Repealed
- 2Authorisation Repealed
- 3Labelling Repealed
- 4Monitoring for environmental effects Repealed
- 5Register Repealed
- 6Authorisation holder Repealed
- 7Repeal Repealed
- 8Validity Repealed
- 9Addressee Repealed
- Annex Repealed
- (a)Applicant and authorisation holder Repealed
- (b)Designation and specification of the products Repealed
- (c)Labelling Repealed
- (d)Method for detection Repealed
- (e)Unique identifier Repealed
- (f)Information required under Annex II to the Cartagena Protocol on Biosafety to the Convention on Biological Diversity Repealed
- (g)Conditions or restrictions on the placing on the market, use or handling of the products Repealed
- (h)Monitoring plan Repealed
- (i)Post-market monitoring requirements for the use of the food for human consumption Repealed
- Repealed
1Genetically modified organism and unique identifierF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
2AuthorisationF1
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3LabellingF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4Monitoring for environmental effectsF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
5RegisterF1
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6Authorisation holderF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
7RepealF1
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8ValidityF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
9AddresseeF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(a)Applicant and authorisation holderF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(b)Designation and specification of the productsF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(c)LabellingF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(d)Method for detectionF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(e)Unique identifierF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(f)Information required under Annex II to the Cartagena Protocol on Biosafety to the Convention on Biological DiversityF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(g)Conditions or restrictions on the placing on the market, use or handling of the productsF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(h)Monitoring planF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(i)Post-market monitoring requirements for the use of the food for human consumptionF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .