Genetically Modified Organisms - food and feed
Comments to the EFSA public hearing of genetically modified maize MON 88017 (EFSA-GMO-RX-014)
Report no: Comments to EFSA
The Norwegian Committee for Food and Environment (VKM) has performed a preliminary assessment of a renewal application for authorisation of the genetically modified maize event MON 88017 in the EEA. The scope of the application includes all uses of MON 88017 and sub-combinations independently of their origin equivalent to the uses of any other maize grain and forage.
The assessment was performed in connection with EFSA´s (European Food Safety Authorities) public hearing of the renewal application EFSA-GMO-RX-014, on request from the Norwegian Food Safety Authority and the Norwegian Environment Agency.
The assessment of maize MON 88017 is based on information provided by the applicant in the application EFSA-GMO-RX-014 and relevant peer-reviewed scientific literature.
Maize MON 88017 provides tolerance to glyphosate based herbicides, and protection from feeding damage caused by coleopteran target pests. Commission decision of 2009 authorised the placing of products containing, consisting of, or produced from genetically modified maize MON 88017 on the EU market. The authorisation was granted for a period of ten years.
Authorisation process for genetically modified organisms
Through the EEA Agreement, the EU Directive 2001/18/EC on deliberate release into the environment of genetically modified organisms is implemented in Norwegian law. Norway is therefore affiliated with the GMO authorisation process in the EU. In the EU, both GMOs and derived products are regulated by the Directive and Regulation 1829/2003/EC. The Regulation concerns genetically modified food and feed and is currently not a part of the EEA Agreement. In preparation for a legal implementation of the Regulation in Norwegian law, Norway follows the EU proceedings for GMO applications.
Applicants wishing to extend the authorisation period for genetically modified organisms apply for renewal. EFSA submits the application for a public hearing across all EEA countries. VKM conducts its own review of the application and sends its comments to EFSA. EFSA then completes their scientific opinion based on information from the applicant, comments from EEA countries and independent literature. The scientific opinion is then issued to the European Commission.
VKM submitted comments to the application EFSA-GMO-RX-014 to EFSA on March 16th 2019.