The U.S. Food and Drug Administration’s (FDA) final regulation on good manufacturing practices (GMPs) for dietary supplements (21 CFR 111) established stringent requirements for companies involved with the manufacturing, packaging, labeling and holding of dietary supplements.
Under the rule, manufacturers are required to evaluate the identity, purity, quality, strength, and composition of their dietary ingredients and dietary supplements. GMPs are crucial to the supplement industry’s ability to deliver safe, accurately labeled products to the consumer and in achieving the public health benefits noted by Congress in the preamble to the Dietary Supplement Health and Education Act of 1994.
You can read the full guidance here, but why not let us assist you in becoming compliant or maintaining compliance without you having to read, interpret and implement the FDA Guidance? Contact Us Today!