GMP (Good Manufacturing Practice) refer to the Good Manufacturing Practice Regulations promulgated by the US Food and Drug Administration under the authority of the Federal Food, Drug and Cosmetic Act.

These regulations, which have the force of law require that manufactures, processors and packagers of drugs, medical device, some food, and blood take proactive steps to ensure that their products are safe, pure, and effective, GMP regulation require a quality approach to manufacturing, enabling companies to minimize or eliminate instance of contamination, mix-ups, and error.

This is turn, protects the consumer from purchasing a product, which is not effective or even dangerous.

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