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New animal drugs in genetically engineered animals (21 CFR 528.1070-528.2010).

Country/Territory
United States of America
Document type
Regulation
Date
2009 (2015)
Source
FAO, FAOLEX
Original source
Code of Federal Regulations - Title 21 - Food and Drugs.
Subject
Livestock
Keyword
Drugs Procedural matters Classification/declassification Genetically modified organism (GMO) Animal health
Geographical area
Americas, Arctic, East Pacific, North America, North Atlantic
Abstract

Part 528 of Title 21 of the Federal Code of Regulations prescribes the technical and procedural issues regarding the application/use of new animal drugs in genetically engineered animals.

Full text
English
Website
www.gpo.gov

References - Legislation

Implements

Federal Food, Drug, and Cosmetic Act (21 U.S.C. 301-399d).

Legislation | United States of America | 1938 (2021)

Keyword: Basic legislation, Food quality control/food safety, Hygiene/sanitary procedures, Packaging/labelling, Food additives, Residues, MRL-maximum residue limit, Standards, Registration, Inspection, Traceability/product tracing, Treated food, HACCP, Fish products, Fraud, Enforcement/compliance, Offences/penalties, Pesticides, Animal health, Animal feed/feedstuffs, Drugs

Source: FAO, FAOLEX