Commission Decision
of 19 May 2004
authorising the placing on the market of sweet corn from genetically modified maize line Bt11 as a novel food or novel food ingredient under Regulation (EC) No 258/97 of the European Parliament and of the Council
(notified under document number C(2004) 1865)
(only the Dutch text is authentic)
(2004/657/EC)
THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Whereas:
On 11 February 1999, Novartis (in the meantime: Syngenta), submitted a request to the competent authorities of the Netherlands for placing sweet maize from genetically modified maize line Bt11 on the market as a novel food or as a novel food ingredient.
In their initial assessment report of 12 May 2000, the Netherlands’ competent food assessment body came to the conclusion that Bt11 sweet maize is as safe as conventional sweet maize.
The Commission forwarded the initial assessment report to all Member States on 15 June 2000. Within the 60 days period laid down in Article 6(4) of the Regulation, reasoned objections to the marketing of the product were raised in accordance with that provision.
On 13 December 2000, the Commission requested an opinion from the Scientific Committee on Food, in accordance with Article 11 of the Regulation. On 17 April 2002, the Scientific Committee on Food delivered its opinion that Bt11 sweet maize is as safe for human food use as its conventional counterparts. This opinion focused, as requested by the Commission, on the issues raised in the comments made by Member States’ authorities, including molecular characterisation and toxicity studies. The concerns raised in the opinion of the ‘Agence française de sécurité sanitaire des aliments’ (AFSSA) of 26 November 2003 do not bring any new scientific elements in addition to the initial assessment of sweet maize Bt11.
The Joint Research Centre (JRC) of the European Commission, in collaboration with the European Network of GMO Laboratories (ENGL), has carried out a full validation study (ring-trial) following internationally accepted guidelines to test the performance of a quantitative event-specific method to detect and quantify the Bt11 transformation event in sweet maize. The method validated had been developed by the National Veterinary Institute of Norway and INRA, France. The materials needed in the study (GM and non-GM DNA as well as the method-specific reagents) had been provided by Syngenta. The JRC has considered that the method performance was appropriate for its aimed purpose, taken into account the performance criteria proposed by the ENGL for methods submitted for regulatory compliance as well as the current scientific understanding about satisfactory method performance. Both the method and the results of the validation have been made publicly available.
Reference material for sweet maize from genetically modified maize line Bt11 has been produced by the Joint Research Centre (JRC) of the European Commission.
Information on the identification of sweet maize from genetically modified maize line Bt11, including the validated detection method and the reference material, contained in the annex, shall be retrievable from the Register to be established by the Commission in accordance with Article 28 of Regulation (EC) No 1829/2003.
Genetically modified maize Bt11 has been notified to the Biosafety Clearing-House, pursuant to Articles 11(1) and 20(3)(c) of the Cartagena Protocol on Biosafety to the Convention on Biological Diversity.
However, the Council has not acted within the required time limit; a Decision should now be adopted by the Commission,
HAS ADOPTED THIS DECISION:
Article 1
Sweet maize from genetically modified maize line Bt11 (hereinafter referred to as the product), as designated and specified in the Annex, may be placed on the Community market as a novel food or novel food ingredient.
Article 2
The product shall be labelled as ‘genetically modified sweet maize’, in accordance with the labelling requirements laid down in Article 13 of Regulation (EC) No 1829/2003.
Article 3
The product and the information included in the Annex shall be entered in the Community register of genetically modified food and feed.
Article 4
This Decision is addressed to Syngenta Seeds BV, Westeinde 62, 1600 AA Enkhuizen, The Netherlands, representing Syngenta Seeds AG, Switzerland. It shall be valid for a period of 10 years.
Done at Brussels, 19 May 2004.
For the Commission
David Byrne
Member of the Commission
ANNEXInformation to be entered in the Community Register of Genetically Modified Food and Feed
- (a) Authorisation holder
- Name
Syngenta Seeds BV
- Address
Westeinde 62, 1600 AA Enkhuizen, The Netherlands
- On behalf of
Syngenta Seeds AG, Schwarzwaldallee 215, CH-4058 Basel, Switzerland
- Name
- (b) Designation and specification of the product
Sweet maize, fresh or canned, that is progeny from traditionally crosses of traditionally bred maize with genetically modified maize line Bt11 that contains:
a synthetic version of the cryIA (b) gene derived from Bacillus thuringiensis kurstaki strain HD1 under the control of a 35S promoter from Cauliflower Mosaic Virus, and IVS 6 intron from the maize alcohol dehydrogenase gene and the nopaline synthase terminator sequence of Agrobacterium tumefaciens, and
a synthetic version of the pat gene derived from Streptomyces viridochromogenes under the control of a 35S promoter from Cauliflower Mosaic Virus, an IVS intron from the maize alcholdehydrogenase gene and the nopaline synthase terminator sequence of Agrobacterium tumefaciens.
- (c) Labellin
‘Genetically modified sweet maize’
- (d) Method for detection
Event specific real-time quantitative PCR based method for genetically modifiedBt11 sweet maize, published in European Food Research and Technology, Vol. 216/2003, pages 347-354.
Validated by the Joint Research Centre (JRC) of the European Commission, in collaboration with the European Network of GMO Laboratories (ENGL), published at http://engl.jrc.it/crl/oj/bt11sm.pdf.
Reference Material: IRMM-412R, produced by the Joint Research Centre (JRC) of the European Commission.
- (e) Unique identifier
SYN-BT Ø11-1
- (f) Information required under Annex II to the Cartagena Protocol
Biosafety Clearing House, Record ID 1240
(see: http://bch.biodiv.org/Pilot/Record.aspx?RecordID=1240)
- (g) Conditions or restrictions on the placing on the market of the product
Not applicable
- (h) Post-market monitoring requirements
Not appropriate