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