Before a GMO can be approved, the public has 30 days to comment:
- on the summary of the applications submitted under Directive 2001/18/EC.
- on the risk assessment done by the European Food Safety Authority (EFSA) for applications submitted under Regulation (EC) 1829/2003 (see below).
After the consultation, the Commission sends the comments received for the applications submitted under Directive 2001/18/EC directly to the lead competent authority for analysis. Scientific comments received for the applications submitted under Regulation (EC) 1829/2003 are sent to EFSA who checks their impact on the EFSA scientific opinion.
Assessment of genetically modified soybean A5547-127 for renewal under Regulation (EC) No 1829/2003 (application EFSA-GMO-RX-020).
Oilseed rape MS11
EFSA statement complementing the EFSA Scientific Opinion on application for authorisation of food and feed containing, consisting of and produced from genetically modified oilseed rape MS11.
Maize DP4114 × MON 810 × MIR604 × NK603 and subcombinations
Assessment of genetically modified maize DP4114 × MON 810 × MIR604 × NK603 and subcombinations, for food and feed uses, under Regulation (EC) No 1829/2003 (application EFSA-GMO-NL-2018-150)
Maize NK603 x T25 x DAS-40278-9
Assessment of genetically modified maize NK603 x T25 x DAS-40278-9 and its subcombinations for food and feed uses, under Regulation (EC) No 1829/2003 (application EFSA‐GMO‐NL‐2019‐164)
Consultations from previous years
- Consultations 2021
- Consultations 2020
- Consultations 2019
- Consultations 2018
- Consultations 2017
- Consultations 2016
- Consultations 2015
- Consultations 2014
- Consultations 2013
- Consultations 2012
- Consultations 2011
- Consultations 2010
- Consultations 2009
- Consultations 2008
- Consultations 2007
- Consultations 2006
- Consultations 2005