FDA 21 CFR

FDA 21 CFR (Code of Federal Regulations Title 21) is a set of rules and standards established by the U.S. Food and Drug Administration to regulate the safety, effectiveness, and quality of food, drugs, medical devices, and cosmetics. It ensures that products are properly tested, labeled, and manufactured to protect public health. The regulations provide guidance for companies on how to develop, produce, and market their products compliantly. Essentially, 21 CFR acts as a legal framework to ensure that consumers receive safe and effective products and that companies adhere to consistent quality controls.