40 CFR Part 161 - DATA REQUIREMENTS FOR REGISTRATION OF ANTIMICROBIAL PESTICIDES
- SUBPART A — General Provisions (§§ 161.20 - 161.85)
- SUBPART B — How To Use Data Tables (§§ 161.100 - 161.108)
- SUBPART C — Product Chemistry Data Requirements (§§ 161.150 - 161.190)
- SUBPART D — Data Requirement Tables (§§ 161.202 - 161.640)
- Appendix A to Part 161 - Data Requirements for Registration: Use Pattern Index
Title 40 published on 2012-07-01
The following are only the Rules published in the Federal Register after the published date of Title 40.
For a complete list of all Rules, Proposed Rules, and Notices view the Rulemaking tab.
GPO FDSys XML | Text type regulations.gov FR Doc. 2013-04613 RIN 2070-AJ26 EPA-HQ-OPP-2010-0427 FRL-9372-7 ENVIRONMENTAL PROTECTION AGENCY Final rule. This final rule is effective April 29, 2013. 40 CFR Parts 152, 158 and 161 With this final rule EPA declares a prion ( i.e., proteinaceous infectious particle) to be a “pest” under the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) and amends the regulations to expressly include prion within the regulatory definition of pest. This final rule also amends existing pesticide product performance data requirements to clarify that efficacy data are required for pesticide products with prion-related claims. In addition, EPA is announcing the availability of final test guidelines on generating the product performance data for prion-related pesticide products.
Title 40 published on 2012-07-01
The following are ALL rules, proposed rules, and notices (chronologically) published in the Federal Register relating to 40 CFR 161 after this date.
GPO FDSys XML | Text type regulations.gov FR Doc. 2013-10162 RIN 2070-AD30 EPA-HQ-OPP-2008-0110 FRL-8886-5 ENVIRONMENTAL PROTECTION AGENCY Final rule. This final rule is effective July 8, 2013. 40 CFR Parts 158 and 161 EPA is revising the data requirements for antimicrobial pesticide products to reflect current scientific and regulatory practice, and to provide the regulated community with clearer and transparent information about the data needed to support pesticide registration decisions for antimicrobial products. The updated data requirements also serve to further enhance EPA's ability to make regulatory decisions about the human health, and environmental fate and effects of antimicrobial pesticide products. These revisions are also expected to help protect human health and the environment by providing an up-to-date scientific framework for identifying and assessing the risks of antimicrobial pesticides sold or distributed in the United States.
GPO FDSys XML | Text type regulations.gov FR Doc. 2013-04613 RIN 2070-AJ26 EPA-HQ-OPP-2010-0427 FRL-9372-7 ENVIRONMENTAL PROTECTION AGENCY Final rule. This final rule is effective April 29, 2013. 40 CFR Parts 152, 158 and 161 With this final rule EPA declares a prion ( i.e., proteinaceous infectious particle) to be a “pest” under the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) and amends the regulations to expressly include prion within the regulatory definition of pest. This final rule also amends existing pesticide product performance data requirements to clarify that efficacy data are required for pesticide products with prion-related claims. In addition, EPA is announcing the availability of final test guidelines on generating the product performance data for prion-related pesticide products.
GPO FDSys XML | Text type regulations.gov FR Doc. 2012-19406 RIN 2070-AJ26 EPA-HQ-OPP-2010-0427 FRL-9357-9 ENVIRONMENTAL PROTECTION AGENCY Notification of submission to the Secretaries of Agriculture and Health and Human Services. 40 CFR Parts 152, 158 and 161 This document notifies the public as required by the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) that the EPA Administrator has forwarded to the Secretary of the United States Department of Agriculture (USDA) and the Secretary of the United States Department of Health and Human Services (HHS) a draft regulatory document concerning Declaration of Prion as a Pest Under FIFRA; Related Amendments; and Availability of Final Test Guidelines. The draft regulatory document is not available to the public until after it has been signed and made available by EPA.