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Context of 'Early January 2001: Biotech Consultant Says Biotech Industry Hopes to Force Acceptance of GM Foods by Making Them Prevalent'

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Over the span of two decades, Monsanto accumulates approximately 650 plant-related biotech patents, including the patent on the 35S promoter, a genetic mechanism used extensively in the biotech industry. All biotech companies using the promoter must pay Monsanto a technology use fee. By 2004, the company has a 29.82 percent share of all research and development in the biotech industry. [Center for Food Safety, 2005, pp. 13 pdf file]

Entity Tags: Monsanto

Timeline Tags: Seeds

Anti-abortion activist Don Benny Anderson tries to burn down two women’s clinics in Florida. [Kushner, 2003, pp. 38]

Entity Tags: Don Benny Anderson

Timeline Tags: US Health Care, Domestic Propaganda, US Domestic Terrorism

Vice President Dan Quayle, chairman of the President’s Council on Competitiveness, and Louis Sullivan, secretary of health and human services, announce the FDA’s new policy on the regulation of genetically engineered foods. In the policy statement that is published three days later, the FDA will say it has determined that genetically modified (GM) foods are “substantially equivalent” to conventionally grown foods and therefore will not be subject to any special regulations. The agency justifies its position saying that assessments concerning the safety of food products should be based on the characteristics of the food product and not on the methods used to develop that product. [US Food and Drug Administration, 5/29/1992 pdf file] Specifically addressing the issue of labeling for GM foods, the May 29 statement will read: “The agency is not aware of any information showing that foods derived by these new methods differ from other foods in any meaningful or uniform way, or that, as a class, foods developed by the new techniques present any different or greater safety concern than foods developed by traditional plant breeding. For this reason, the agency does not believe that the method of development of a new plant variety… would… usually be required to be disclosed in labeling for the food.” Labeling would only be required in special cases, the FDA says. For example, if a genetically engineered tomato contains a peanut protein that is a proven allergen, a label will be needed. [US Food and Drug Administration, 5/29/1992, pp. 22991 pdf file] In their statement to the press, Sullivan says that biotechnology promises to develop new food products “that are tastier, more varied, more wholesome, and that can be produced more efficiently.” Quayle’s council played a key role in expediting the development of the policy. [Food and Drug Administration, 5/26/1992] Quayle explains that the policy will ensure the competitiveness of US firms. “The reforms we announce today will speed up and simplify the process of bringing better agricultural products, developed through biotech, to consumers, food processors, and farmers,” he says. “We will ensure that biotech products will receive the same oversight as other products, instead of being hampered by unnecessary regulation.” [New York Times, 1/25/2001]

Entity Tags: Dan Quayle, Louis Sullivan, US Food and Drug Administration

Timeline Tags: Seeds

Don Westfall, vice president of biotech consulting company Promar International, tells the Toronto Star, “The hope of the [biotech] industry is that over time the market is so flooded [with GM food products] that there’s nothing you can do about it. You just sort of surrender.” [Toronto Star, 1/9/2001]

Entity Tags: Don Westfall

Timeline Tags: Seeds

Defense Department spokesman Lt. Cmdr. Don Sewell asserts in an email to the San Francisco Chronicle, “The Army and all other components of [Defense Department] have no plans, programs, or intentions to develop chemical or biological weapons prohibited by statute or treaty.” [San Francisco Chronicle, 6/9/2003]

Entity Tags: Don Sewell

Timeline Tags: US Military

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