by Jon Rappoport
March 1, 2013
Perhaps you remember the ill-fated Just-Label-It campaign. A number of activist groups petitioned the FDA for a federal regulation that would make labeling GMO food mandatory.
The petition amassed over a million signatures. But the FDA decided only 394 of these were legitimate, because all the others were electronically submitted in one document.
Infuriating? Of course. But that was nothing. Let’s get down to the core of the crime.
Imagine this. A killer is put on trial, and the jury, in a surprise verdict, finds him not guilty. Afterwards, reporters interview this killer. He says, “The jury freed me. It’s up to them. They decide. That’s what justice is all about.”
Then the press moves along to members of the jury, who say: Well, we had to take the defendant’s word. He said he was innocent, so that’s what we ruled.
That’s an exact description of the FDA and Monsanto partnership.
When you cut through the verbiage that surrounded the introduction of GMO food into America, you arrive at two key statements. One from Monsanto and one from the FDA, the agency responsible for overseeing, licensing, and certifying new food varieties as safe.
Quoted in the New York Times Magazine (October 25, 1998, “Playing God in the Garden”), Philip Angell, Monsanto’s director of corporate communications, famously stated: “Monsanto shouldn’t have to vouchsafe the safety of biotech food. Our interest is in selling as much of it as possible. Assuring its safety is the FDA’s job.”
From the Federal Register, Volume 57, No.104, “Statement of [FDA] Policy: Foods Derived from New Plant Varieties,” here is what the FDA had to say on this matter: “Ultimately, it is the food producer who is responsible for assuring safety.”
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