Before a company can register its pesticide products with the EPA, it must know what the EPA considers a pesticide under the law. According to section 2(u) of FIFRA, 7 U.S.C. section 136(u), the term "pesticide" is defined as the following: • any substance or mixture of substances intended for preventing, destroying, repelling, or mitigating any pest, • any substance or mixture of substances intended for use as a plant regulator, defoliant, or desiccant, and • any nitrogen stabilizer, except that the term "pesticide" shall not include any article that is a "new animal drug" within the meaning of section 321(w)[1] of title 21, that has been determined by the Secretary of Health and Human Services not to be a new animal drug by a regulation establishing conditions of use for the article, or that is an animal feed within the meaning of section 321(x)[1] of title 21 bearing or containing a new animal drug. The term "pesticide" does not include liquid chemical sterilant products (including any sterilant or subordinate disinfectant claims on such products) for use on a critical or semi-critical device, as defined in section 321 of title 21. For purposes of the preceding sentence, the term "critical device" includes any device which is introduced directly into the human body, either into or in contact with the bloodstream or normally sterile areas of the body and the term "semi-critical device" includes any device which contacts intact mucous membranes but which does not ordinarily penetrate the blood barrier or otherwise enter normally sterile areas of the body. An applicant will have to prove that the pesticide active ingredient, pesticide product, or proposed new use of a registered pesticide will not cause unreasonable adverse effects on human health and environment. There is considerable public interest in the contents of pesticide registration studies, which has led to conflict over public access to these materials. These competing interests as well as legislation addressing access has been covered separately under
Pesticide regulation in the United States. In some cases, manufacturers choose to conduct addition work to satisfy requirements for peer-reviewed literature, as was the case for the herbicide,
cloransulam-methyl. Publication of registration studies in the peer-reviewed literature not only provides unlimited public access, but also ensures sufficient rigor to satisfy the scientific community at large. Under Section 408 of the
Federal Food, Drug, and Cosmetic Act (FFDCA), the EPA can also regulate the amount of pesticide residues permissible on or in food/feed items, by establishing a "safe" level meaning there is "a reasonable certainty of no harm" from the exposure to the residue whether directly from the consumption of such food or from other non-occupational sources. The
Food Quality Protection Act (FQPA), amended FIFRA to require all older pesticides to cause no harm to infants, children, and sensitive individuals within "reasonable certainty". Through the reregistration program, older pesticides are eligible for reregistration if they have a complete database and not cause unreasonable health and environmental risks if used as directed in accordance to their labels. FQPA also requires the EPA to review pesticides on a 15-year cycle to ensure all pesticides meet contemporary safety and regulatory standards.
Fees Initial and final fees for reregistration of food or feed use active ingredients are $50,000 and $100,000-$150,000, respectively. Reregistration fees for non-food use pesticides are $50,000-$100,000. Annual maintenance fees are also imposed: $425 per product up to fifty products and a maximum of $20,000 per company. For each product over fifty, the fee is $100, for a maximum fee of $35,000. Fees may be reduced or waived for small business registrants, public health pesticides, or minor use pesticides at the EPA's discretion, and failure to pay reregistration fees or maintenance fees may result in cancellation of a product registration. ==Regulated non-pesticidal products not requiring registration==