Comment Re:Authority (Score 1) 510
The irony here is that the FDA itself conducts no scientific review.
As reported last October: (emphasis added)
Q: Does the FDA test these foods before they're allowed on the market?
A: No. Instead there is a voluntary consultation process. Genetically engineered foods are overseen by the FDA, but there is no approval process. Foods are presumed to be safe unless the FDA has evidence to the contrary, Jaffe says. The FDA "has to show that there may be a problem with the food, as opposed to the company needing to prove it's safe to FDA's satisfaction before it can get on the market," he says.
And from the horse's mouth itself: (emphasis added)
[Section V B] It is the responsibility of the producer of a new food to evaluate the safety of the food and assure that the safety requirement of section 402(a)(1) of the act is met. In section VII., FDA provides guidance to the industry regarding prudent, scientific approaches to evaluating the safety of foods derived from new plant varieties, including the safety of the added substances that are subject to section 402(a)(1) of the act. FDA encourages informal consultation between producers and FDA scientists to ensure that safety concerns are resolved. However, producers remain legally responsible for satisfying section 402(a)(1) of the act, and they will continue to be held accountable by FDA through application of the agency's enforcement powers.
Also, the basis for the fallacious assumption that genes introduced from other species are not worth rigorous testing: (emphasis added)
[excerpted Section V C] With respect to transferred genetic material (nucleic acids), generally FDA does not anticipate that transferred genetic material would itself be subject to food additive regulation. Nucleic acids are present in the cells of every living organism, including every plant and animal used for food by humans or animals, and do not raise a safety concern as a component of food. In regulatory terms, such material is presumed to be GRAS. Although the guidance provided in section VII. calls for a good understanding of the identity of the genetic material being transferred through genetic modification techniques, FDA does not expect that there will be any serious question about the GRAS status of transferred genetic material.
"Obviously GMO organisms are safe because we have no expectations they won't be safe." Most people would call BS on that kind of self-fulfilling prophecy. Does the FDA really not understand it's how those nucleic acids are arranged, not just what nucleic acids are present?
