www.checkbiotech.org ; www.raupp.info ; www.czu.cz

The European Commission has authorised the placing on the market of three
oilseed rapes known as Ms8, Rf3 and Ms8xRf3, genetically modified for
tolerance to the herbicide glufosinate-ammonium. This decision is valid for
10 years and covers the use of the oilseed rapes for imports and processing
into animal feed or for industrial purposes, March 2007.

It includes measures to be taken by the company who developed the GM
oilseed rapes to prevent any damage to health and the environment in the
event of accidental spillage. Processed oil derived from these GM oilseed
rapes has already been approved for food use in 1999 and 2000 in the EU.

The authorisation covers the import and the use of Ms8, Rf3 and Ms8xRf3
oilseed rapes as animal feed, but not cultivation or food uses. These
genetically modified oilseed rapes are tolerant to the herbicide
glufosinate-ammonium and do not contain an antibiotic resistance marker
gene. They have been subject to a rigorous pre-market risk assessment and
have been scientifically assessed by the Member States, as well as the
European Food Safety Authority, as being as safe as any conventional oilseed
rape.

When put on the market, products containing Ms8, Rf3 or Ms8xRf3 will need to
be clearly labelled as containing genetically modified oilseed rape. They
will be covered by the strict labelling and traceability rules in force
since April 2004. The labelling will provide operators and consumers with
the information they need to decide whether to buy the product or not.

Robust post-marketing rules will ensure that the product can be traced and
monitored once put on the market, thanks to a unique identifier assigned to
the oilseed rape products. In addition, the authorisation includes a set of
guidelines to Bayer, the company who developed the oilseed rape, on how to
deal appropriately with accidental spillage should it occur.

During the past six years, the EU has put in place a clear, transparent and
stringent system to regulate genetically modified food, feed and crops. The
authorisation procedure under this new system ensures that only genetically
modified organisms (GMOs) which are safe for human and animal consumption
and for release into the environment can be placed on the European market.
Individual authorisations are granted following appraisal of the GMOs in
question on a case by case basis. Requests for authorisations which do not
fulfil all criteria have been and will continue to be rejected.

This is the sixth authorising decision to be issued under the Directive of
2001 on the deliberate release into the environment of GMOs.

In January 2003, Bayer submitted a request to the competent authorities of
Belgium for placing genetically modified oilseed rapes Ms8, Rf3 and Ms8xRf3
on the market. The initial request was for import, processing, feed use and
cultivation, but not food use.
The Belgian authorities came to the conclusion that Ms8, Rf3 and Ms8xRf3
oilseed rapes are as safe as conventional oilseed rapes and should be placed
on the market for import and processing and for use as any other oilseed
rape but not for the requested use of cultivation.

The European Food Safety Authority also appraised the application and
focused on the scientific issues raised by competent authorities from the
other Member States. Its opinion similarly concluded that Ms8, Rf3 and
Ms8xRf3 oilseed rapes were as safe as conventional oilseed rapes.

The Regulatory Committee established under Directive 2001/18 on the
deliberate release into the environment of GMOs did not give an opinion in
December 2005. The Commission therefore submitted a proposal to the Council.

The proposal was considered by the Agriculture and Fisheries Council on 18
September 2006. At that meeting the Council did not reach a qualified
majority either for or against the Commission proposal. Consequently, under
the legal "comitology" procedure, the Commission must adopt the Decision.
The Commission?s decision to approve Ms8, Rf3 and Ms8xRf3 is therefore
designed to ensure that this legal framework is correctly and fully applied
by Member States.

This includes post-market monitoring of the continued safety of the product
once it has been placed on the market via the use of surveillance systems.
This monitoring is required throughout the period of validity of the
consent. Reports of this monitoring programme must be submitted to all
Member States and the Commission on an annual basis.

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