Submission of Unreasonable Adverse Effects Information Under FIFRA Section 6(a)(2) (Renewal)

Section 6(a)(2) of the Federal Insecticide, Fungicide and Rodenticide Act (FIFRA) requires pesticide registrants to submit information to the Agency which may be relevant to the balancing of the risks and benefits of a pesticide product. The statute requires the registrant to submit any factual information that it acquires regarding adverse effects associated with its pesticidal products, and it is up to the Agency to determine whether or not that factual information constitutes an unreasonable adverse effect. In order to limit the amount of less meaningful information that might be submitted to the Agency, the EPA has limited the scope of factual information that the registrant must submit. The Agencys regulations at 40 CFR part 159 provide a detailed description of the reporting obligations of registrants under FIFRA section 6(a)(2).

The latest form for Submission of Unreasonable Adverse Effects Information Under FIFRA Section 6(a)(2) (Renewal) expires 2021-02-28 and can be found here.

FIFRA Section 6(a)(2) Submisssions - Studies

Federal Enterprise Architecture: Environmental Management - Pollution Prevention and Control