Explanatory Memorandum to COM(2007)403 - Authorisation of the placing on the market of products containing, consisting of, or produced from genetically modified maize NK603xMON810 (MON-ØØ6Ø3-6xMON-ØØ81Ø-6) pursuant to Regulation 1829/2003 (Only the French and Dutch texts are authentic) - Main contents
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| dossier | COM(2007)403 - Authorisation of the placing on the market of products containing, consisting of, or produced from genetically modified ... |
|---|---|
| source | COM(2007)403  |
| date | 12-07-2007 |
The attached proposal also concerns the placing on the market of other products containing or consisting of NK603xMON810 maize for the same uses as any other maize with the exception of cultivation.
On 31 March 2006, the European Food Safety Authority ('EFSA') gave a favourable opinion in accordance with Articles 6 and 18 of Regulation (EC) No 1829/2003 and concluded that it is unlikely that the placing on the market of the products containing, consisting of, or produced from NK603xMON810 maize as described in the application will have adverse effects on human or animal health or the environment i. In its opinion, EFSA concluded that it was acceptable to use the data for the single events in support of the safety of the products and considered all specific questions and concerns raised by the Member States in the context of the consultation of the national competent authorities provided for by Article 6 i and 18 i of that Regulation.
Against this background, a draft Commission Decision authorising the placing on the Community market of products containing, consisting of, or produced from genetically modified NK603xMON810 maize was submitted to the Standing Committee on the Food Chain and Animal Health, on 8 June 2007, for vote. The Committee delivered no opinion : fifteen Member States (214 votes) voted in favour, nine Member States (86 votes) voted against and three Member States (45 votes) abstained.
Consequently, pursuant to Article 35, paragraph 2 of Regulation (EC) No 1829/2003 and in accordance with Article 5 of Council Decision 1999/468/EC modified by Council Decision 2006/512/EC, the Commission is required to submit to the Council a proposal relating to the measures to be taken, the Council having three months in which to act by a qualified majority, and inform the Parliament.
Contents
- Proposal for a
- Article 1 Genetically modified organism and unique identifier
- Article 2 Authorisation
- Article 3 Labelling
- Article 4 Monitoring for environmental effects
- Article 5Community register
- Article 6Authorisation holder
- Article 7Validity
- Article 8Addressee
- For the Council
- MON-ØØ6Ø3-6xMON-ØØ81Ø-6
COUNCIL DECISION
authorising the placing on the market of products containing, consisting of, or produced from genetically modified maize NK603xMON810 (MON-ØØ6Ø3-6xMON-ØØ81Ø-6) pursuant to Regulation (EC) No 1829/2003 of the European Parliament and of the Council
(Only the French and Dutch texts are authentic)
(Text with EEA relevance)
THE COUNCIL OF THE EUROPEAN UNION,
Having regard to the Treaty establishing the European Community,
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 i, and in particular Article 7 i and Article 19 i thereof,
Whereas:
On 1 June 2004, Monsanto Europe S.A., submitted to the competent authorities of The United Kingdom 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 NK603xMON810 maize ('the application').
The application also covers the placing on the market of other products containing or consisting of NK603xMON810 maize for the same uses as any other maize with the exception of cultivation. Therefore, in accordance with the provision of Articles 5 i and 17 i of Regulation (EC) No 1829/2003, it includes the data and information required by Annexes III and IV to 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 i and information and conclusions about the risk assessment carried out in accordance with the principles set out in Annex II to Directive 2001/18/EC.
On 31 March 2006, the European Food Safety Authority (‘EFSA’) gave a favourable opinion in accordance with Articles 6 and 18 of Regulation (EC) No 1829/2003 and concluded that it is unlikely that the placing on the market of the products containing, consisting of, or produced from NK603xMON810 maize as described in the application ('the products') will have adverse effects on human or animal health or the environment i. In its opinion, EFSA concluded that it was acceptable to use the data for the single events in support of the safety of the products and considered all specific questions and concerns raised by the Member States in the context of the consultation of the national competent authorities provided for by Articles 6 i and 18 i of that Regulation.
In October 2006, upon request of the Commission, EFSA published detailed clarifications on how the comments of the competent authorities of the Member States had been taken into account in its opinion. It also published further information on the different elements considered by the Scientific Panel on Genetically Modified Organisms of EFSA and the reason why some specific additional studies such as a 90-day toxicology study in rats were not considered as necessary.
In its opinion, EFSA also concluded that the environmental monitoring plan, consisting of a general surveillance plan, submitted by the applicant is in line with the intended use of the products.
Taking into account those considerations, authorisation should be granted for the products.
A unique identifier should be assigned to each GMO as provided for in 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 i.
On the basis of the EFSA opinion, no specific labelling requirements other than those provided for in Articles 13 i and 25 i of Regulation (EC) No 1829/2003 appear to be necessary for the foods, food ingredients, and feed containing, consisting, or produced from NK603xMON810 maize. However, in order to ensure the use of the products within the limits of authorisation provided by this Decision, the labelling of feed containing or consisting of the GMO and other products than food and feed containing or consisting of the GMO for which authorisation is requested should be complemented by a clear indication that the products in question must not be used for cultivation.
Similarly, the EFSA opinion does not justify the imposition of specific conditions or restrictions for the placing on the market and/or specific conditions or restrictions for the use and handling, including post-market monitoring requirements, or of specific conditions for the protection of particular ecosystems/environment and/or geographical areas, as provided for in point (e) of Articles 6 i and 18 i of Regulation (EC) No 1829/2003.
All relevant information on the authorisation of the products should be entered in the Community register of genetically modified food and feed as provided for in Regulation (EC) No 1829/2003.
Article 4 i of 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 i, lays down labelling requirements for products consisting or containing GMOs.
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 Article 9 i and Article 15(2)(c) of Regulation (EC) No 1946/2003 of the European Parliament and of the Council of 15 July 2003 on transboundary movements of genetically modified organisms i.
The Standing Committee on the Food Chain and Animal Health has not delivered an opinion within the time-limit laid down by its Chairman and the measures provided for in this Decision must therefore be adopted by the Council.
HAS ADOPTED THIS DECISION:
Genetically modified maize ( Zea mays L.) NK603xMON810 produced by crosses between maize containing MON-ØØ6Ø3-6 and MON-ØØ81Ø-6 events, as specified in point (b) of the Annex to this Decision, is assigned the unique identifier MON-ØØ6Ø3-6xMON-ØØ81Ø-6, as provided for in Regulation (EC) No 65/2004.
The following products are authorised for the purposes of Articles 4 i and 16 i of Regulation 1829/2003, in accordance with the conditions set out in this Decision :
(a) foods and food ingredients containing, consisting of, or produced from MON-ØØ6Ø3-6xMON-ØØ81Ø-6 maize;
(b) feed containing, consisting of, or produced from MON-ØØ6Ø3-6xMON-ØØ81Ø-6 maize;
(c) products, other than food and feed, containing or consisting of MON-ØØ6Ø3-6xMON-ØØ81Ø-6 maize for the same uses as any other maize with the exception of cultivation.
1. For the purposes of the labelling requirements laid down in Articles 13 i and 25 i of Regulation (EC) No 1829/2003 and in Article 4 i of Regulation (EC) N°1830/2003, the ’name of the organism’ shall be ’maize’.
2. The words ‘not for cultivation’ shall appear on the label of and in documents accompanying products containing or consisting of MON-ØØ6Ø3-6xMON-ØØ81Ø-6 maize referred to in Article 2(b) and (c).
1. The authorisation holder shall ensure that the monitoring plan for environmental effects, as set out in the 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.
The information set out in the Annex to this Decision shall be entered in the Community register of genetically modified food and feed, as provided for in Article 28 of Regulation (EC) No 1829/2003.
The authorisation holder shall be Monsanto Europe S.A., Belgium, representing Monsanto Company, United States of America.
This Decision shall apply for a period of 10 years from the date of its notification.
This Decision is addressed to Monsanto Europe S.A., Scheldelaan 460, Haven 627 – B 2040 Antwerp – Belgium.
Done at Brussels,
The President
ANNEX
(a) Applicant and Authorisation holder:
Name: Monsanto Europe S.A.
Address: Scheldelaan 460, Haven 627 – B 2040 Antwerp – Belgium
On behalf of Monsanto Company - 800 N. Lindbergh Boulevard – St. Louis, Missouri 63167 - United States of America
(b) Designation and specification of the products:
Foods and food ingredients containing, consisting of, or produced from MON-ØØ6Ø3-6xMON-ØØ81Ø-6 maize;
Feed containing, consisting of, or produced from MON-ØØ6Ø3-6xMON-ØØ81Ø-6 maize;
Products other than food and feed containing or consisting of MON-ØØ6Ø3-6xMON-ØØ81Ø-6 maize for the same uses as any other maize with the exception of cultivation.
The genetically modified maize MON-ØØ6Ø3-6xMON-ØØ81Ø-6, as described in the application, is produced by crosses between maize containing MON-ØØ6Ø3-6 and MON-ØØ81Ø-6 events and expresses the CP4 EPSPS protein which confers tolerance to the glyphosate herbicide and the Cry1Ab protein which confers protection against certain lepidopteran insect pests ( Ostrinia nubilalis, Sesamia spp.).
(c) Labelling:
For the purposes of the labelling requirements laid down in Articles 13 i and 25 i of Regulation (EC) No 1829/2003 and in Article 4 i of Regulation (EC) n° 1830/2003, the ’name of the organism’ shall be ’maize’.
The words ‘not for cultivation’ shall appear on the label of and in documents accompanying products containing or consisting of MON-ØØ6Ø3-6xMON-ØØ81Ø-6 maize referred to in Article 2(b) and (c).
(d) Method for detection:
- Event specific real-time quantitative PCR based methods for genetically modified maize MON-ØØ6Ø3-6 and MON-ØØ81Ø-6 maize validated on MON-ØØ6Ø3-6xMON-ØØ81Ø-6 maize.
- Validated by the Community reference laboratory established under Regulation (EC) No 1829/2003, published at gmo-crl.jrc.it/statusofdoss
- Reference Material: ERM®-BF413 (for MON-ØØ81Ø-6) and ERM®-BF415 (for MON-ØØ6Ø3-6) accessible via the Joint Research Centre (JRC) of the European Commission, the Institute of Reference Materials and Measurements (IRMM) at www.irmm.jrc.be/html
(e) Unique identifier:
(f) Information required under Annex II to the Cartagena Protocol on Biosafety to the Convention on Biological Diversity:
Biosafety Clearing House, Record ID: see [ to be completed when notified ]
(g) Conditions or restrictions on the placing on the market, use or handling of the products:
Not required.
(h) Monitoring plan
Monitoring plan for environmental effects conforming with Annex VII to Directive 2001/18/EC.
[Link: plan published on the internet]
(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 the time. Those modifications will be made available to the public via the updating of the Community register of genetically modified food and feed.