From: RickieB19@aol.com Sent: Monday, March 26, 2001 10:17 AM To: fdadockets@oc.fda.gov Subject: Docket 00N-1396 & Docket 00D-1598 This email is to advocate for genetically engineered products to be labeled and tested for safety. Please require mandatory pre-market safety testing, r equire pre-market environmental review, require mandatory labeling of GE foods, no restriction on voluntary Labeling of non-GE foods, strict notification of intent to genetically engineer products, thorough assessment and testing for years prior to the marketing of a GE food, ensure public access to adequate information for independent review, and listen to consumer groups. * 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 for your consideration of this request. Fredrika Block l89-04 64th Ave - 10C Fresh Meadows, NY ll365