Federal (United States) · Regulations
Subpart D — Reporting Requirements for Risk/Benefit Information
15 sections
15 sections
- 40 C.F.R. § 159.152What the law requires of registrants.
- 40 C.F.R. § 159.153Definitions.
- 40 C.F.R. § 159.155When information must be submitted.
- 40 C.F.R. § 159.156How information must be submitted.
- 40 C.F.R. § 159.158What information must be submitted.
- 40 C.F.R. § 159.159Information obtained before promulgation of the rule.
- 40 C.F.R. § 159.160Obligations of former registrants.
- 40 C.F.R. § 159.165Toxicological and ecological studies.
- 40 C.F.R. § 159.167Discontinued studies.
- 40 C.F.R. § 159.170Human epidemiological and exposure studies.
- 40 C.F.R. § 159.178Information on pesticides in or on food, feed or water.
- 40 C.F.R. § 159.179Metabolites, degradates, contaminants, and impurities.
- 40 C.F.R. § 159.184Toxic or adverse effect incident reports.
- 40 C.F.R. § 159.188Failure of performance information.
- 40 C.F.R. § 159.195Reporting of other information.