Commission Implementing Decision (EU) 2021/66 of 22 January 2021 authorising the placing on the market of products containing, consisting of or produced from genetically modified soybean MON 87751 × MON 87701 × MON 87708 × MON 89788, pursuant to Regulation (EC) No 1829/2003 of the European Parliament and of the Council (notified under document C(2021) 285) (Only the Dutch text is authentic) (Text with EEA relevance)

Type Implementing Decision
Publication 2021-01-26
Last updated 2026-07-29
State In force
Department European Commission, SANTE
Source EUR-Lex
articles 9
Reform history JSON API

Article 1

Genetically modified organism and unique identifier

Genetically modified soybean (Glycine max (L.) Merr) MON 87751 × MON 87701 × MON 87708 × MON 89788, as specified in point (b) of the Annex to this Decision, is assigned the unique identifier MON-87751-7 × MON 877Ø1-2 × MON-877Ø8-9 × MON-89788-1, in accordance with Regulation (EC) No 65/2004.

Article 2

Authorisation

The following products are authorised for the purposes of Articles 4(2) and 16(2) of Regulation (EC) No 1829/2003 in accordance with the conditions set out in this Decision:

Article 3

Labelling
1.

For the purposes of the labelling requirements laid down in Articles 13(1) and 25(2) of Regulation (EC) No 1829/2003 and in Article 4(6) of Regulation (EC) No 1830/2003, the ‘name of the organism’ shall be ‘soybean’.

2.

The words ‘not for cultivation’ shall appear on the label of and in the documents accompanying products containing or consisting of genetically modified soybean MON-87751-7 × MON 877Ø1-2 × MON-877Ø8-9 × MON-89788-1, with the exception of products referred to in point (a) of Article 2.

Article 4

Method for detection

The method set out in point (d) of the Annex shall apply for the detection of genetically modified soybean MON-87751-7 × MON 877Ø1-2 × MON-877Ø8-9 × MON-89788-1 as referred to in Article 1.

Article 5

Monitoring for environmental effects
1.

The authorisation holder shall ensure that the monitoring plan for environmental effects, as set out in point (h) of the Annex, is put in place and implemented.

2.

The authorisation holder shall submit to the Commission annual reports on the implementation and the results of the activities set out in the monitoring plan in accordance with the format set out in Decision 2009/770/EC.

Article 6

Community register

The information set out in the Annex shall be entered in the Community register of genetically modified food and feed, as referred to in Article 28(1) of Regulation (EC) No 1829/2003.

Article 7

Authorisation holder

The authorisation holder shall be Bayer CropScience LLC, United States, represented in the Union by Bayer Agriculture B.V., Belgium.

Article 8

Validity

This Decision shall apply for a period of 10 years from the date of its notification.

Article 9

Addressee

This Decision is addressed to Bayer CropScience LLC, 800 N. Lindbergh Boulevard St. Louis, Missouri 63167, United States, represented in the Union by Bayer Agriculture B.V., Scheldelaan 460, 2040 Antwerp, Belgium.

ANNEX

(a) Applicant and authorisation holder:

Name: Bayer CropScience LLC

Address: 800 N. Lindbergh Boulevard St. Louis, Missouri 63167, United States,

represented in the Union by: Bayer Agriculture B.V., Scheldelaan 460, 2040 Antwerp, Belgium.

(b) Designation and specification of the products

The genetically modified soybean MON-87751-7 × MON 877Ø1-2 × MON--877Ø8-9 × MON-89788-1 expresses the dmo gene, which confer tolerance to dicamba based herbicides, the cp4 epsps gene which confers tolerance to glyphosate based herbicides, the cry1Ac, cry2Ab2 and cry1A.105 genes, which confer protection against certain lepidopteran pests.

(c) Labelling

(d) Method for detection

(e) Unique identifier

MON-87751-7 × MON 877Ø1-2 × MON-877Ø8-9 × MON-89788-1.

(f) Information required under Annex II to the Cartagena Protocol on Biosafety to the Convention on Biological Diversity

[Biosafety Clearing-House, Record ID number: published in the Community register of genetically modified food and feed when notified].

(g) Conditions or restrictions on the placing on the market, use or handling of the products

Not required.

(h) Monitoring plan for environmental effects

Monitoring plan for environmental effects in accordance with Annex VII to Directive 2001/18/EC.

[Link: plan published in the Community register of genetically modified food and feed]

(i) Post-market monitoring requirements for the use of the food for human consumption

Not required.

Note : Links to relevant documents may need to be modified over time. Those modifications will be made available to the public via the updating of the Community register of genetically modified food and feed.

Reading this document does not replace reading the official text published in the Official Journal of the European Union. We assume no responsibility for any inaccuracies arising from the conversion of the original to this format.

This text is published under EUR-Lex's own terms of reuse, not a Legalize or public-domain licence. EUR-Lex
Creative Commons Attribution 4.0 International (CC BY 4.0)
© European Union, https://eur-lex.europa.eu — Source: EUR-Lex (Publications Office of the European Union). Reused under the Creative Commons Attribution 4.0 International (CC BY 4.0) licence. Only EU legislation published in the printed Official Journal of the European Union is deemed authentic; consolidated texts are reproduced here for documentation purposes and have been reformatted to Markdown.