Author:
,Mullins Ewen,Bresson Jean‐Louis,Dalmay Tamas,Dewhurst Ian Crawford,Epstein Michelle M.,Firbank Leslie George,Guerche Philippe,Hejatko Jan,Moreno Francisco Javier,Naegeli Hanspeter,Nogué Fabien,Rostoks Nils,Sanchez Serrano Jose Juan,Savoini Giovanni,Veromann Eve,Veronesi Fabio,Casacuberta Josep,Afonso Ana,Lenzi Paolo,Papadopoulou Nikoletta,Raffaello Tommaso
Abstract
Abstract
EFSA was asked by the European Parliament to provide a scientific opinion on the analysis by the French Agency for Food, Environmental and Occupational Health & Safety (ANSES) of Annex I of the European Commission proposal for a regulation ‘on plants obtained by certain new genomic techniques (NGTs) and their food and feed, and amending regulation (EU) 2017/625’. The Panel on genetically modified organisms (GMO) assessed the opinion published by ANSES, which focuses on (i) the need to clarify the definitions and scope, (ii) the scientific basis for the equivalence criteria and (iii) the need to take potential risks from category 1 NGT plants into account. The EFSA GMO Panel considered the ANSES analysis and comments on various terms used in the criteria in Annex I of the European Commission proposal and discussed definitions based on previous EFSA GMO Panel opinions. The EFSA GMO Panel concluded that the available scientific literature shows that plants containing the types and numbers of genetic modifications used as criteria to identify category 1 NGT plants in the European Commission proposal do exist as the result of spontaneous mutations or random mutagenesis. Therefore, it is scientifically justified to consider category 1 NGT plants as equivalent to conventionally bred plants with respect to the similarity of genetic modifications and the similarity of potential risks. The EFSA GMO Panel did not identify any additional hazards and risks associated with the use of NGTs compared to conventional breeding techniques in its previous Opinions.