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欧盟授权转基因大豆MON 87751 (MON-87751-7)及其产品投放市场

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放大字体  缩小字体 2019-08-12 02:32:52  来源:欧盟委员会  浏览次数:174
核心提示:欧盟授权转基因大豆MON 87751 (MON-87751-7)及含有转基因大豆MON 87751 (MON-87751-7)的产品投放市场,规定了转基因玉米及其产品的标签、授权持有人、有效期限及决定送达人等,附件详细规定了产品的名称和规格、对环境影响的监测、检测方法等。
发布单位
欧盟委员会,欧盟健康与食品安全署
欧盟委员会,欧盟健康与食品安全署
发布文号 实施决定 (EU) 2019/1309
发布日期 2019-07-26 生效日期 2019-08-02
有效性状态 废止日期 2029-08-02
属性 专业属性 产品及原料
备注 欧盟授权转基因大豆MON 87751 (MON-87751-7)及含有转基因大豆MON 87751 (MON-87751-7)的产品投放市场,规定了转基因玉米及其产品的标签、授权持有人、有效期限及决定送达人等,附件详细规定了产品的名称和规格、对环境影响的监测、检测方法等。
 COMMISSION IMPLEMENTING DECISION (EU) 2019/1309

of 26 July 2019

authorising the placing on the market of products containing, consisting of or produced from genetically modified soybean MON 87751 (MON-87751-7), pursuant to Regulation (EC) No 1829/2003 of the European Parliament and of the Council

(notified under document C(2019) 5489)

(only the Dutch and French texts are authentic)

(Text with EEA relevance)

 

THE EUROPEAN COMMISSION,

Having regard to the Treaty on the Functioning of the European Union,

Having regard to Regulation (EC) No 1829/2003 of the European Parliament and of the Council of 22 September 2003 on genetically modified food and feed (1), and in particular Articles 7(3) and 19(3) thereof,
Whereas:
(1)On 26 September 2014, Monsanto Europe S.A./N.V. submitted on behalf of Monsanto company, United States, an application, in accordance with Articles 5 and 17 of Regulation (EC) No 1829/2003, for the placing on the market of foods, food ingredients and feed containing, consisting of or produced from genetically modified soybean MON 87751 (‘the application’) to the national competent authority of the Netherlands. The application also covered the placing on the market of products containing or consisting of genetically modified soybean MON 87751 for uses other than food and feed, with the exception of cultivation.
(2)In accordance with Articles 5(5) and 17(5) of Regulation (EC) No 1829/2003, the application included information and conclusions about the risk assessment carried out in accordance with the principles set out in Annex II to Directive 2001/18/EC of the European Parliament and of the Council (2) and the information required by Annexes III and IV to that Directive. It also included a monitoring plan for environmental effects in accordance with Annex VII to Directive 2001/18/EC.
(3)On 2 August 2018, the European Food Safety Authority (‘the Authority’) issued a favourable opinion in accordance with Articles 6 and 18 of Regulation (EC) No 1829/2003 (3). The Authority concluded that genetically modified soybean MON 87751, as described in the application, is as safe as and nutritionally equivalent to its conventional counterpart and the tested non-genetically modified soybean reference varieties, with respect to the potential effects on human and animal health and the environment.
(4)In its opinion, the Authority considered all the questions and concerns raised by the Member States in the context of the consultation of the national competent authorities as provided for by Articles 6(4) and 18(4) of Regulation (EC) No 1829/2003.
(5)The Authority also concluded that the monitoring plan for environmental effects consisting of a general surveillance plan, submitted by the applicant, was in line with the intended uses of the products.
(6)Taking those conclusions into account, the placing on the market of products containing, consisting of or produced from genetically modified soybean MON 87751 should be authorised for the uses listed in the application.
(7)By letter dated 27 August 2018, Monsanto Europe N.V. informed the Commission that Monsanto Europe N.V. converted its legal form and changed its name to Bayer Agriculture BVBA, Belgium.
(8)A unique identifier should be assigned to genetically modified soybean MON 87751 in accordance with Commission Regulation (EC) No 65/2004 (4).
(9)On the basis of the Authority's opinion, no specific labelling requirements, other than those provided for in Articles 13(1) and 25(2) of Regulation (EC) No 1829/2003 and in Article 4(6) of Regulation (EC) No 1830/2003 of the European Parliament and of the Council (5), appear to be necessary for the products covered by this Decision. However, in order to ensure that the use of those products remains within the limits of the authorisation granted by this Decision, the labelling of the products containing or consisting of genetically modified soybean MON 87751, with the exception of food products, should contain a clear indication that they are not intended for cultivation.
(10)In order to account for the implementation and the results of the activities set out in the monitoring plan for environmental effects, the authorisation holder should submit annual reports, presented in accordance with the standard reporting format requirements laid down in Commission Decision 2009/770/EC (6).
(11)The opinion of the Authority does not justify the imposition of specific conditions or restrictions for the placing on the market, for the use and handling, including post-market monitoring requirements regarding the consumption of the food and feed, or for the protection of particular ecosystems/environment or geographical areas, as provided for in Articles 6(5)(e) and 18(5)(e) of Regulation (EC) No 1829/2003.
(12)All relevant information on the authorisation of the products should be entered in the Community register of genetically modified food and feed referred to in Article 28(1) of Regulation (EC) No 1829/2003.
(13)This Decision is to be notified through the Biosafety Clearing-House to the Parties to the Cartagena Protocol on Biosafety to the Convention on Biological Diversity, pursuant to Articles 9(1) and 15(2)(c) of Regulation (EC) No 1946/2003 of the European Parliament and of the Council (7).
(14)The Standing Committee on Plants, Animals, Food and Feed has not delivered an opinion within the time limit laid down by its Chairman. This implementing act was deemed to be necessary and the chair submitted it to the appeal committee for further deliberation. The appeal committee did not deliver an opinion,

HAS ADOPTED THIS DECISION:

Article 1

Genetically modified organism and unique identifier

Genetically modified soybean (Glycine max (L.) Merr.) MON 87751, as specified in point (b) of the Annex to this Decision, is assigned the unique identifier MON-87751-7, 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:
(a)foods and food ingredients containing, consisting of or produced from genetically modified soybean MON-87751-7;
(b)feed containing, consisting of or produced from genetically modified soybean MON-87751-7;
(c)products containing or consisting of genetically modified soybean MON-87751-7 for uses other than those provided for in points (a) and (b), with the exception of cultivation.

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, 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.

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 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 Monsanto Company, United States, represented by Bayer Agriculture BVBA, 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 Agriculture BVBA, Scheldelaan 460, 2040 Antwerp, Belgium.

Done at Brussels, 26 July 2019.

For the Commission

Vytenis ANDRIUKAITIS

Member of the Commission


(1)  OJ L 268, 18.10.2003, p. 1.

(2)  Directive 2001/18/EC of the European Parliament and of the Council of 12 March 2001 on the deliberate release into the environment of genetically modified organisms and repealing Council Directive 90/220/EEC (OJ L 106, 17.4.2001, p. 1).

(3)  EFSA GMO Panel (EFSA Panel on genetically Modified Organisms), 2018. Scientific opinion on the assessment of genetically modified soybean MON 87751 for food and feed uses under Regulation (EC) No 1829/2003 (application EFSA-GMO-NL-2014–121). EFSA Journal 2018; 16(8):5346, 32 pp. doi: 10.2903/j.efsa.2018.5346

(4)  Commission Regulation (EC) No 65/2004 of 14 January 2004 establishing a system for the development and assignment of unique identifiers for genetically modified organisms (OJ L 10, 16.1.2004, p. 5).

(5)  Regulation (EC) No 1830/2003 of the European Parliament and of the Council of 22 September 2003 concerning the traceability and labelling of genetically modified organisms and the traceability of food and feed products produced from genetically modified organisms and amending Directive 2001/18/EC (OJ L 268, 18.10.2003, p. 24).

(6)  Commission Decision 2009/770/EC of 13 October 2009 establishing standard reporting formats for presenting the monitoring results of the deliberate release into the environment of genetically modified organisms, as or in products, for the purpose of placing on the market, pursuant to Directive 2001/18/EC of the European Parliament and of the Council (OJ L 275, 21.10.2009, p. 9).

(7)  Regulation (EC) No 1946/2003 of the European Parliament and of the Council of 15 July 2003 on transboundary movements of genetically modified organisms (OJ L 287, 5.11.2003, p. 1).


ANNEX

 

 

(a)Applicant and authorisation holder:
Name:Monsanto Company
Address:800 N. Lindbergh Boulevard, St. Louis, Missouri 63167, United States of America
Represented by Bayer Agriculture BVBA, Scheldelaan 460, 2040 Antwerp, Belgium.
(b)Designation and specification of the products:
(1)foods and food ingredients containing, consisting of or produced from genetically modified soybean MON-87751-7;
(2)feed containing, consisting of or produced from genetically modified soybean MON-87751-7;
(3)products containing or consisting of genetically modified soybean MON-87751-7 for uses other than those provided in points (1) and (2), with the exception of cultivation.
The genetically modified soybean MON-87751-7 was developed to confer protection against certain lepidopteran pests through the expression of cry1A.105 and cry2Ab2 genes.
(c)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 documents accompanying the products containing or consisting of genetically modified soybean MON-87751-7, with the exception of products referred to in point (b)(1) of this Annex.
(d)Method for detection:
(1)Event-specific real time quantitative PCR detection methods for genetically modified soybean MON-87751-7.
(2)Validated by the EU Reference Laboratory established under Regulation (EC) No 1829/2003, published at http://gmo-crl.jrc.ec.europa.eu/statusofdossiers.aspx;
(3)Reference Material: AOCS 0215-A is accessible via the American Oil Chemists' Society (AOCS) at https://www.aocs.org/crm.
(e) Unique identifier:
MON-87751-7
(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.

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