Abstract |
The guidance provides information to assist in the preparation of Phase 3 response for reregistration of products. Phase 3 of reregistration is part of a five-phase process for the accelerated reregistration of pesticides established by Section 4 of the Federal Insecticide, Fungicide and Rodenticide Act (FIFRA). In Phase 3, registrants who seek reregistration but who are not eligible for a generic data exemption must determine which of their previously submitted scientific studies are adequate to support reregistration. The document contains guidance required by Section 4(e) of FIFRA concerning the adequacy of studies, how studies must be summarized and reformatted, and how to identify information on adverse effects. |