Full-text source covering federal and state laws and regulations and court decisions that govern the safety, effectiveness, purity, packaging and labeling of food, drugs and cosmetics. Devoted primarily to the Federal Food, Drug and Cosmetic Act, the Fair Packaging and Labeling Act and the Comprehensive Drug Prevention and Control Act.
Learn More »Upon application and review, the FDA may designate a country as not subject to bovine spongiform encephalopathy (BSE, “mad cow disease”) restrictions applicable to human food and cosmetics manufactured from, processed with, or that otherwise contain: specified risk materials, the small intestine of cattle (unless the distal ileum is removed), material from nonambulatory disabled cattle, or mechanically separated beef. Amending the definition of “ prohibited cattle materials” in two previous interim final rules, the FDA concurred with previously submitted comments that it was not necessary for all BSE-related restrictions to apply to human food and cosmetics regardless of a country's BSE status. Cattle materials inspected and passed from a country that receives the new designation will not be considered. FDA Interim Final Rule, ¶40,341D.
For more information regarding this topic, see the Food, Drug and Cosmetics Law Reporter. The Reporter provides the full-text source covering federal and state laws and regulations and court decisions that govern the safety, effectiveness, purity, packaging and labeling of food, drugs and cosmetics. Devoted primarily to the Federal Food, Drug and Cosmetic Act, the Fair Packaging and Labeling Act and the Comprehensive Drug Prevention and Control Act. Learn more.
Food, Drug and Cosmetics Law Reporter
Everything you need to know about Food and Drug Regulations.Full-text source covering federal and state laws and regulations and court decisions that govern the safety, effectiveness, purity, packaging and labeling of food, drugs and cosmetics. Learn More » |
Medical Devices ReporterAccess the full text plus expert analysis of all laws and regulations governing the classification, approval, manufacture, and marketing of all medical diagnostic, and radiological devices. Learn More » |