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FDA Critical of GMO Labeling Bill

The Food and Drug Administration has sent the Senate Agriculture Committee technical comments on the genetically modified food labeling bill that Senate Agriculture Committee Chairman Pat Roberts, R-Kan., and ranking member Debbie Stabenow, D-Mich., have developed in an attempt to preempt state labeling laws. The technical comments surfaced as both sides in the labeling debate are making arguments to the Senate on whether the bill should be passed. The FDA noted that the bill would give USDA labeling authority in an area that is usually reserved for the FDA and that FDA has long held that foods developed with genetic engineering are safe and do not require labeling.

But the FDA also said that: -- Provisions to allow information regarding the GE (genetically engineered) content of food to be presented only in an electronically accessible form and not on the package label would be in tension with FDA's statute and regulations, which require disclosures on food labels. -- The definition of "bioengineering" would result in a somewhat narrow scope of coverage because it leaves out food without genetic material, which means that oil made from genetically engineered soybeans would not be covered. -- It appears that the intent is to have the bill apply to all foods except those that are essentially meat, poultry, or eggs, and that the drafters may have assumed, incorrectly, that products covered by the Federal Meat Inspection Act, the Poultry Products Inspection Act, or the Egg Products Inspection Act are not covered by the Food, Drug and Cosmetic Act. -- Language regarding exceptions and inclusions is unclear.

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