In accordance with an assignment specified by the Norwegian Food Safety Authority (NFSA) and the Norwegian Environment Agency (NEA), VKM assesses whether genetically modified organisms (GMOs) intended for the European market can pose risks to human or animal health, or the environment in Norway. VKM assesses the scientific documentation regarding GMO applications seeking approval for use of GMOs as food and feed, processing, or cultivation.

The EU Regulation 1829/2003/EC (Regulation) covers living GMOs that fall under the Norwegian Gene Technology Act, as well as processed food and feed from GMOs (dead material) that fall under the Norwegian Food Act. The regulation is currently not part of the EEA agreement or implemented in Norwegian law.

Norway conducts its own assessments of GMO applications in preparation for the possible implementation of the Regulation.

In accordance with the assignment by NFSA and NEA, VKM assesses GMO applications during scientific hearings initiated by the European Food Safety Authority (EFSA), as well as after EFSA has published its own risk assessment of a GMO, up until EU member countries vote for or against approval in the EU Commission. The assignment is divided into three stages.

Genetically modified oilseed rape MON 94100 × MON 88302 × RF3

MON 94100 × MON 88302 × RF3 oilseed rape was produced by crossing oilseed rape plants containing MON 94100, MON 88302 and RF3 by traditional breeding methods. MON 94100 × MON 88302 × RF3 expresses the DMO enzyme from MON 94100 conferring tolerance to the herbicide dicamba, CP4 EPSPS enzyme from MON 88302 conferring tolerance to the herbicide glyphosate, the enzyme PAT/bar conferring tolerance to the herbicide glufosinate-ammonium and the male fertility-restorer protein from RF3.

The scientific documentation provided in the application for genetically modified oilseed rape MON 94100 × MON 88302 × RF3 is adequate for risk assessment, and in accordance with EFSA guidance on risk assessment of genetically modified plants for use in food or feed. The VKM GMO panel does not consider the introduced modifications in oilseed rape MON 94100 × MON 88302 × RF3 to imply potential specific health or environmental risks in Norway, compared to EU-countries.

Therefore, VKM had no comments to EFSA regarding the application GMFF-2022-11270 during EFSA's scientific hearing.

Previous assessments of oilseed rape MON 94100 × MON 88302 × RF3 by VKM

No

About the assignment

The assignment is divided into three stages.

In stage 1, VKM shall assess the health and environmental risks of the genetically modified organism and derived products in connection with the EFSA scientific hearing of GMO applications. VKM shall review the scientific documentation that the applicant has submitted and possibly provide comments to EFSA. VKM must also consider: i) whether there are specific Norwegian conditions that could give other risks in Norway than those mentioned in the application, ii) whether the Norwegian diet presents a different health risk for the Norwegian population should the GMO be approved, compared to the European population, and iii) risks associated with co-existence with conventional and/or ecologic production of plants for GMOs seeking approval for cultivation. Relevant measures to ensure co-existence must also be considered.

In stage 2, VKM shall assess whether comments from Norway have been satisfactorily answered by EFSA. In addition, VKM shall assess whether comments from other countries imply need for further follow-up.

If EFSAs response to Norwegian comments is not satisfactory, or comments by other countries imply the need for further follow-up, VKM shall in stage 3 perform a risk assessment of these conditions, including conditions specific to Norway.