From: Katrina [katrina@maui.net] Sent: Tuesday, April 03, 2001 8:57 PM To: fdadocket@oc.fda.gov Subject: Docket OON-1396 & Docket 00D-1598 Thank you for your time and consideration in reading these comments. Sincerely, Katrina Pitman Kula, Maui, Hawaii > > FOR THE SAKE OF THE ENVIRONMENT AND FUTURE > > GENERATIONS > > > > TELL THE FDA THAT GENETICALLY ENGINEERED PRODUCTS > > MUST BE LABELED AND TESTED FOR SAFETY! > > > > The Food and Drug Administration is now accepting public > > comment on its proposed new rules on genetically engineered > > (GE) foods. Despite overwhelming consumer demand, the FDA > > has failed to require health and ecological safety testing > > or mandatory labeling, and thus puts your health and our > > environment at risk and deprives you of the right to know > > or choose what you are eating. > > > > The proposed rules: > > > > * Do not require mandatory pre-market safety testing > > * Do not require pre-market environmental review > > * Do not require mandatory labeling of GE foods > > * Restrict voluntary labeling of non-GE foods > > * Require a mere letter of notification prior to the > > marketing of a GE food > > * Fail to ensure public access to adequate information > > for independent review > > * Are supported by industry and opposed by consumer groups > > > > The FDA needs to hear from hundreds of thousands of Americans > > that: > > > > * The FDA must require mandatory pre-market comprehensive > > environmental review. Unlike conventional pollutants, > > where a given amount of pollutant causes a limited amount > > of damage, a small number of mutant genes could have a > > population explosion and reproduce forever, causing > > unlimited and irreparable damage. > > > > * The FDA must require mandatory pre-market long-term health > > testing. GE products could be toxic, cause allergic > > responses, have lower nutritional value, and compromise > > immune responses in consumers. > > > > * The FDA must require mandatory labeling of GE products. > > Without mandatory labeling, neither consumers nor health > > professionals will know if an allergic or toxic reaction > > was the result of a genetically engineered food. Consumers > > would be deprived of the critical knowledge needed to hold > > food producers liable should any of these novel products > > be hazardous. > > > > * The FDA must end its cozy relationship with the industries > > it purports to be regulating. People have been allowed to > > work for a biotech company, then work for the FDA writing the > > regulatory rules on that company's product, then go back to > > working for the company. Ninety-two percent of FDA advisory > > committee meetings had at least one conflict of interest. Thank you.