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European Union must reinstate science in GMO safety assessment and eliminate unnecessary animal testing, says EuropaBio


Brussels, Belgium
17 April 2018

Reacting to the outcomes of the EU research projects GRACE, G-TwYST and GMO90+ presented this week, Beat Späth, Director of Agricultural Biotechnology at EuropaBio, calls for an end to unneeded animal testing. “In light of the clear scientific evidence, political interference with GMO risk assessment has to stop,” he said. “If the EU is genuinely serious about being consistent with its own legislation aiming to replace, reduce and refine the use of animals used for scientific purposes and its policy to follow the science, wasteful and unnecessary animal tests should no longer be required.” 

The results of the research projects, which were funded with more than 11 million Euros(1) of European taxpayers’ money, show, yet again, that the mandatory requirement to conduct rodent tests for safety assessment lacks any scientific basis. In 2013, the EU imposed mandatory 90-day animal feeding trials for GM food and feed risk assessment despite the clear scientific advice of the EU’s risk assessment body, the European Food Safety Authority (EFSA), which repeatedly dismissed the mandatory requirement as unnecessary. The requirement remains in clear contradiction with the globally maintained principle of science-based risk assessment.

In 2013, the Commission was instructed to review the requirement for mandatory 90-day feeding studies by 30 June 2016 on the basis of the outcome of the EU research project GRACE. An independent academic consortium of the GRACE project concluded in November 2015 that there is no scientific justification for a mandatory 90-day study. 

Mandatory feeding studies do not add to product safety nor build trust in the EU’s authorisation system for GMO imports.  They only add further to the well-documented unnecessary delays in the process at the needless expense of animals.

“We support the objective of increasing trust in science and in the EU’s safety assessment procedure. One of the lowest hanging fruits is to make sure that the safety assessment requirements are, at the very least, science-based,” added Späth.

 

More details available here: G-TwYST, GRACE, GMO90+.
 
“EU Commission-sponsored Research on Safety of Genetically Modified Organisms’’ (1985-2000): “The use of more precise technology and the greater regulatory scrutiny probably makes GMOs even safer than conventional plants and foods.” "A decade of EU-funded GMO research’’ (2001-2010) covering 50 EU projects, more than 400 independent research groups, European research grants of some EUR 300 million.
 
BACKGROUND
 
• Over the past 25 years, the EU has spent well over €300 million on over 50 complementary studies on GMOs,(2)  consistently confirming the world-wide scientific consensus that all safety assessed GM crops are at least as safe as conventionally bred crops.
• Further on the theme of trust in science and decision-making, see also EuropaBio position paper and press release on transparency and sustainability of risk assessment.
• Europe benefits greatly from GM crop imports, and GM maize cultivation in Spain has provided considerable benefits after almost 20 years
• The same GMOs approved in other countries in 2 years often take up to 7 years for import approval in the EU. See EuropaBio’s risk assessment timeline factsheet.
 


More news from: EuropaBio


Website: http://www.europabio.org

Published: April 20, 2018

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