From: Rochella Cooper [cooper@pdq.net] Sent: Wednesday, March 28, 2001 4:49 PM To: fdadockets@oc.fda.gov Subject: Re: Docket 00N-1396 & Docket 00D-1598 GENETICALLY ENGINEERED PRODUCTS MUST BE LABELED AND TESTED FOR SAFETY! This is a request that you..... * Require mandatory pre-market safety testing * Require pre-market environmental review * Require mandatory labeling of GE foods * Encourage voluntary labeling of non-GE foods * Require a more than a letter of notification prior to the marketing of a GE food * Ensure public access to adequate information for independent review * 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. Sent: Wednesday, March 28, 2001 1:01 PM Subject: Docket 00N-1396 & Docket 00D-1598 GENETICALLY ENGINEERED PRODUCTS MUST BE LABELED AND TESTED FOR SAFETY! This is a request that you..... * Require mandatory pre-market safety testing * Require pre-market environmental review * Require mandatory labeling of GE foods * Encourage voluntary labeling of non-GE foods * Require a more than a letter of notification prior to the marketing of a GE food * Ensure public access to adequate information for independent review * 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. Sincerely, Rochella Cooper President Texans for Alternatives to Pesticides