Guest guest Posted June 18, 2003 Report Share Posted June 18, 2003 Tue, 17 Jun 2003 23:23:54 -0700 News Update from The Campaign FDA Policy on GE Foods: from bad to worse News Update From The Campaign to Label Genetically Engineered Foods ---- Dear News Update Subscribers, In an incredible act of irresponsibility, the U.S. Food and Drug Administration (FDA) has backpedaled on their already inadequate policy of regulating genetically engineered foods. In January 2001, the FDA issued " Proposed Rules " that if implemented would have required biotech companies to notify the agency before bringing a new genetically engineered food to market. However, the FDA never issued the " Final Rules " that would have made mandatory notification the law. On Tuesday, FDA Deputy Commissioner Lester Crawford told a Congressional committee that they no longer felt that mandatory notification is a priority. Before introducing the January 2001, Proposed Rules, the FDA had stated they were going to make mandatory consultation a requirement. But when they issued the Proposed Rules, they changed it from mandatory consultation to mandatory notification. Now they are telling the biotech companies they are not even required to notify the FDA before bringing a new product to market. Is it any wonder that European Union nations and countries around the world are concerned about the safety of genetically engineered foods? How can they have trust in the safety of genetically engineered foods when the U.S. agency charged with protecting human health has written themselves out of the regulatory oversight policy? The FDA has essentially said to Monsanto and the other biotech companies, " We trust you to do adequate safety testing. " But can we trust Monsanto? Monsanto is a company that just last year was found guilty in Alabama on issues regarding PCBs on all six charges the jury considered: negligence, wantonness, suppression of the truth, nuisance, trespass and outrage. Will Monsanto suppress the truth when it comes to genetically engineered foods? And what about that " outrage " charge against Monsanto? Under Alabama law, the charge of " outrage " requires conduct " so outrageous in character and extreme in degree as to go beyond all possible bounds of decency so as to be regarded as atrocious and utterly intolerable in civilized society. " In spite of this track record, the FDA is apparently trusting Monsanto and other biotech companies to be honest when it comes to the safety of genetically engineered foods. Perhaps the FDA has more confidence in Monsanto than many concerned citizens from around the world? Is there is a positive side to this new position by the FDA? Well, it does provide those of us questioning the safety of genetically engineered foods with more evidence that the regulatory oversight in the United States is grossly inadequate. And we will use this evidence as we make our case to Congress about the need to label and safety test genetically engineered foods. We expect the labeling and safety testing legislation to get re-introduced before Congress in the next few weeks. We will let you know when to start asking your members of Congress to co-sponsor the legislation. Posted below is an Associated Press article titled " FDA Opts Against Further Biotech Review " that provides further information on the latest FDA policy. Craig Winters Executive Director The Campaign to Label Genetically Engineered Foods The Campaign PO Box 55699 Seattle, WA 98155 Tel: 425-771-4049 Fax: 603-825-5841 E-mail: label Web Site: http://www.thecampaign.org Mission Statement: " To create a national grassroots consumer campaign for the purpose of lobbying Congress and the President to pass legislation that will require the labeling of genetically engineered foods in the United States. " *************************************************************** FDA Opts Against Further Biotech Review Posted on Tue, Jun. 17, 2003 EMILY GERSEMA Associated Press WASHINGTON - Genetically engineered foods from crops that have already been reviewed and approved by two government agencies shouldn't have to jump through a third regulatory hoop at the Food and Drug Administration, an FDA official told Congress Tuesday. FDA Deputy Commissioner Lester Crawford said the agency is inclined to reject a proposal made by the former Clinton administration that would require biotechnology companies to notify the FDA before putting products on the market. Biotech crops are already regulated by the Agriculture Department and the Environmental Protection Agency. " The current system is working, " Crawford told the House Agriculture Committee's subcommittee on research. " Since there is no public health reason to impose mandatory requirements, FDA is not making this rule a priority. " Crawford said he knows of no instance where a company has not voluntarily shared field tests and other information on its biotech products with the FDA. But Greg Jaffe, biotechnology director for the Center for Science in the Public Interest, said that without a regulation requiring it, companies could withhold data. " Under the current system, they could market something without us even knowing it, " Jaffe said. " That is not the best way to ensure the safety or instill consumer confidence in these crops. " Lisa Dry, a spokeswoman for the Biotechnology Industry Organization, said companies share their data with the FDA because after a review, the agency gives them a letter approving the products. Without the letter, a company would never be able to get its biotech crops to market, she said, explaining that food processors require the letter in order to do business. " They treat it as though it were mandatory because if they don't, they won't get a letter of review so that they can sell their product. " The EPA also has a role in checking food safety if a company is seeking approval to grow a crop genetically designed to contain a pesticide to fight insects. The EPA approves those crops only if they are safe for people to eat and if they won't harm the environment. The Agriculture Department is charged with monitoring the safety of biotech crops from the time they are planted until harvest in small field tests. The department approves the crop to go to market if the test results show it will not harm animals and plants, but it does not determine whether it is safe for humans. The subcommittee's chairman, Rep. Frank Lucas, R-Okla., said he's " confident that these three agencies have established a regulatory framework that ensures biotech products are safely developed and field-tested. " ON THE NET Food and Drug Administration: http://www.fda.gov *************************************************************** If you would like to comment on this News Update, you can do so at the forum section of our web site at: http://www.thecampaign.org/forums *************************************************************** --------- Gettingwell- / Vitamins, Herbs, Aminos, etc. To , e-mail to: Gettingwell- Or, go to our group site: Gettingwell SBC DSL - Now only $29.95 per month! Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.