40 CFR 159, Subpart D - Reporting Requirements for Risk/Benefit Information
prev | next
- § 159.152 — What the law requires of registrants.
- § 159.153 — Definitions.
- § 159.155 — When information must be submitted.
- § 159.156 — How information must be submitted.
- § 159.158 — What information must be submitted.
- § 159.159 — Information obtained before promulgation of the rule.
- § 159.160 — Obligations of former registrants.
- § 159.165 — Toxicological and ecological studies.
- § 159.167 — Discontinued studies.
- § 159.170 — Human epidemiological and exposure studies.
- § 159.178 — Information on pesticides in or on food, feed or water.
- § 159.179 — Metabolites, degradates, contaminants, and impurities.
- § 159.184 — Toxic or adverse effect incident reports.
- § 159.188 — Failure of performance information.
- § 159.195 — Reporting of other information.
Title 40 published on 2012-07-01
no entries appear in the Federal Register after this date.
This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.
This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].
It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.
