The emergence and rapid advancement of new genomic techniques (NGTs) have sparked intense legal and policy debates in both health and agricultural biotechnology. NGTs allow for precise and efficient genetic modifications. In the health sector, the first CRISPR-based therapeutics are currently in development and testing, with broad global consensus around their transformative potential. In the agricultural sector, NGTs hold significant promise for enabling higher crop yields, greater varietal diversity, improved climate resilience, and reduced pesticide use.
Regulators have taken different stances towards NGTs. With respect to NGT plants, the United States and several other countries have adopted permissive frameworks that exempt NGT plants with minor genetic changes from strict GMO oversight. In contrast, the European Union, ruled in 2018 that all NGT plants fall under the 2001 GMO Directive - effectively treating them the same as traditional GMOs, subjecting NGT plants to a prohibitively costly and lengthy market authorization process. This stricter regulation of NGT plants has important implications for scientific innovation, investment, and the competitiveness of the EU. In response, the EU has initiated steps toward deregulation. In March 2025, the Council of the European Union agreed on a negotiating mandate for a revised regulatory framework on NGT plants.
Against this background, we will discuss the future of NGT regulation in Europe in two panels. The first panel will examine the scope and implications of the proposed EU deregulation compared to the current regime, with a focus on its impact on public and private sector research. The second panel will discuss one of the most contentious issues in ongoing negotiations: should NGT plants be eligible for patent protection? Across both panels, we will explore the broader consequences of regulatory choices for innovation, competition, and the future of biotechnology in Europe.
Konferenzbeschreibung als pdf (auf Englisch)