Additional CGMPs for Certain Types of Food. Dietary Supplements - 21 CFR Part 111 For additional information, see Dietary Supplements Guidance Documents & Regulatory Information.

Fact Sheet: Dietary Supplement Current Good Manufacturing Practices (CGMPs) and Interim Final Rule (IFR) Facts (June 2007)

Packaging that may come into contact with dietary supplements must be safe and suitable for its intended use and must not be reactive or absorptive or otherwise affect the safety or quality of the dietary supplement.

2007 - Today the FDA took action to help Americans get accurately labeled and properly manufactured dietary supplements, through its final rule establishing dietary supplement CGMPs.

Ready-to-eat food (RTE food) means any food that is normally eaten in its raw state or any other food, including a processed food, for which it is reasonably foreseeable that the food will be eaten without further processing that would significantly minimize biological hazards.

The Dietary Supplement (DS) CGMP rule in 21 CFR part 111 (“the DS CGMP rule”) requires persons who manufacture, package, label, or hold a dietary supplement to establish and follow current good manufacturing practice to ensure the quality of the dietary supplement and to

The U.S. Food and Drug Administration’s (FDA) final regulation on good manufacturing practices (GMPs) for dietary supplements established stringent requirements for companies involved with the manufacturing, packaging, labeling and holding of dietary supplements.

independently certifies manufacturers as meeting GMP requirements. The program is open not just to manufacturers of dietary supplements, but also to manufacturers of ingredients, raw materials, components, and packaging and labeling .

Dietary Supplements. On June 25, 2007, the U.S. Food and Drug Administration (FDA) released the final rule for dietary supplement Current Good Manufacturing Practices (cGMPs). This rule, which establishes uniform standards needed to ensure quality throughout the manufacturing, packaging, labeling, and holding of dietary supplement products, was ...

The regulations set forth in 21 CFR Part 111 are referred to as the current Good Manufacturing Practices (cGMPs). They represent the minimum standards required to produce and safe and effective dietary supplement.