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When used in parts 101 through 117 of this subchapter, the meaning of the words and phrases listed shall be as defined in this part.
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.
§ 151 - Preparation and sale of worthless or harmful products for domestic animals prohibited; preparation to be in compliance with rules at licensed establishments
§ 152 - Importation regulated and prohibited
§ 153 - Inspection of imports; denial of entry and destruction
§ 154 - Regulations for preparation and sale; licenses
§ 154a - Special licenses for special circumstances; expedited procedure; conditions; exemptions; criteria
§ 155 - Permits for importation
§ 156 - Licenses conditioned on permitting inspection; suspension of licenses
§ 157 - Inspection
§ 158 - Offenses; punishment
§ 159 - Enforcement; penalties applicable; Congressional findings
Title 9 published on 2015-01-01
The following are ALL rules, proposed rules, and notices (chronologically) published in the Federal Register relating to 9 CFR Part 101 after this date.
We are proposing to amend the Virus-Serum-Toxin Act regulations concerning records and reports. This change would require veterinary biologics licensees and permittees to record and submit reports concerning adverse events associated with the use of biological products they produce or distribute. The information that must be included in the adverse event reports submitted to the Animal and Plant Health Inspection Service would be provided in separate guidance documents. This proposed rule replaces a previously published proposed rule, which we are withdrawing as part of this document.