1.0 - Dietary Supplement 21 CFR 111 Definitions 111.455Glossary of the definitions and interpretations of the terms found in section 201 of the Federal Food, Drug, and Cosmetic Act applied to such terms when used in part 21 CFR 111 for dietary supplement good manufacturing practice or GMP.
performed during the development of a new drug product
You must provide water that is safe and sanitary
or reprocess
Each person involved in manufacturing
You must hold components and dietary supplements under appropriate conditions of temperature
apart from supplying medicinal products to the public
and maintaining plants and trees
or other extraneous material
Personnel shall practice good sanitation and health habits
and sanitizing operations
For the production of dietary supplements you must use equipment and utensils that are of appropriate design
and experience